[ CAS No. 7254-29-7 ] {[proInfo.proName]}

Name: 7254-29-7|2-Amino-5-nitropyrimidin-4(1H)-one|95%
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DV 2D 3D

3d Animation Molecule Structure of 7254-29-7

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Quality Control of [ 7254-29-7 ]

COA NMR CNMR HPLC LC-MS

Related Doc. of [ 7254-29-7 ]

SDS Specification

Alternatived Products of [ 7254-29-7 ]

Product Details of [ 7254-29-7 ]

CAS No. :	7254-29-7	MDL No. :	MFCD22495111
Formula :	C₄H₄N₄O₃	Boiling Point :	-
Linear Structure Formula :	-	InChI Key :	XQMCRIHJUALWCL-UHFFFAOYSA-N
M.W :	156.10	Pubchem ID :	252091
Synonyms :

Calculated chemistry of [ 7254-29-7 ] Expand+

Physicochemical Properties

Num. heavy atoms :	11
Num. arom. heavy atoms :	6
Fraction Csp3 :	0.0
Num. rotatable bonds :	1
Num. H-bond acceptors :	4.0
Num. H-bond donors :	2.0
Molar Refractivity :	38.08
TPSA :	117.59 Å²

Pharmacokinetics

GI absorption :	High
BBB permeant :	No
P-gp substrate :	No
CYP1A2 inhibitor :	No
CYP2C19 inhibitor :	No
CYP2C9 inhibitor :	No
CYP2D6 inhibitor :	No
CYP3A4 inhibitor :	No
Log Kp (skin permeation) :	-8.15 cm/s

Lipophilicity

Log Po/w (iLOGP) :	-0.56
Log Po/w (XLOGP3) :	-1.26
Log Po/w (WLOGP) :	-0.73
Log Po/w (MLOGP) :	-1.83
Log Po/w (SILICOS-IT) :	-1.57
Consensus Log Po/w :	-1.19

Druglikeness

Lipinski :	0.0
Ghose :	None
Veber :	0.0
Egan :	0.0
Muegge :	2.0
Bioavailability Score :	0.55

Water Solubility

Log S (ESOL) :	-0.35
Solubility :	69.5 mg/ml ; 0.445 mol/l
Class :	Very soluble
Log S (Ali) :	-0.71
Solubility :	30.2 mg/ml ; 0.194 mol/l
Class :	Very soluble
Log S (SILICOS-IT) :	-0.57
Solubility :	42.2 mg/ml ; 0.27 mol/l
Class :	Soluble

Medicinal Chemistry

PAINS :	0.0 alert
Brenk :	2.0 alert
Leadlikeness :	1.0
Synthetic accessibility :	2.05

Safety of [ 7254-29-7 ]

Signal Word:	Warning	Class:	N/A
Precautionary Statements:	P280-P305+P351+P338	UN#:	N/A
Hazard Statements:	H302	Packing Group:	N/A
GHS Pictogram:

Application In Synthesis of [ 7254-29-7 ]

* All experimental methods are cited from the reference, please refer to the original source for details. We do not guarantee the accuracy of the content in the reference.

Upstream synthesis route of [ 7254-29-7 ]
Downstream synthetic route of [ 7254-29-7 ]

[ 7254-29-7 ] Synthesis Path-Upstream 1~4

1
[ 7254-29-7 ]
[ 7664-93-9 ]
[ 611-08-5 ]

Reference： [1] American Chemical Journal, 1905, vol. 34, p. 564

2
[ 7254-29-7 ]
[ 77994-12-8 ]

Reference： [1] Angewandte Chemie - International Edition, 2007, vol. 46, # 14, p. 2478 - 2484
[2] Chemistry - An Asian Journal, 2011, vol. 6, # 5, p. 1252 - 1262

3
[ 108-53-2 ]
[ 7254-29-7 ]

Reference： [1] Angewandte Chemie - International Edition, 2007, vol. 46, # 14, p. 2478 - 2484
[2] Chemistry - An Asian Journal, 2011, vol. 6, # 5, p. 1252 - 1262
[3] American Chemical Journal, 1905, vol. 34, p. 564
[4] Patent: US2012/214762, 2012, A1, . Location in patent: Page/Page column 80

4
[ 99968-75-9 ]
[ 7254-29-7 ]

Reference： [1] Journal of the Chemical Society, 1959, p. 3647

[ 7254-29-7 ] Synthesis Path-Downstream 1~8

1
[ 99968-75-9 ]
[ 7254-29-7 ]

Reference： [1]Journal of the Chemical Society,1959,p. 3647

2
[ 108-53-2 ]
[ 7254-29-7 ]

Yield	Reaction Conditions	Operation in experiment
	With sulfuric acid; nitric acid; at 20 - 70℃; for 2.5h;Cooling with ice;	Step 1-Synthesis of 2-amino-5-nitro-3,4-dihydropyrimidin-4-one Concentrated sulfuric acid (2.4 mL) was added to 2-amino-3,4-dihydropyrimidin-4-one (1 g, 9.0 mmol). The mixture was stirred and cooled in ice bath before dropwise addition of concentrated nitric acid (0.56 mL). The mixture was stirred at RT for 30 min before being heated at 70 C. for 2 hr. The mixture was allowed to cool to RT and was slowly added to water (10 mL), cooled in an ice bath. The resultant precipitate was collected by suction filtration, washed with diethyl ether (5 mL) and then thoroughly dried under high vacuum to give the title compound: 1H NMR (250 MHz, DMSO) delta 7.18 (1H, br. s.), 8.61 (1H, br. s.), 8.81 (1H, s); LC-MS: m/z=+156.9 (M+H)+.

Reference： [1]Angewandte Chemie - International Edition,2007,vol. 46,p. 2478 - 2484
[2]Chemistry - An Asian Journal,2011,vol. 6,p. 1252 - 1262
[3]American Chemical Journal,1905,vol. 34,p. 564
[4]Patent: US2012/214762,2012,A1 .Location in patent: Page/Page column 80

3
[ 7254-29-7 ]
[ 79442-02-7 ]

Reference： [1]Journal of Heterocyclic Chemistry,1981,vol. 18,p. 671 - 673

5
[ 7254-29-7 ]
[ 7664-93-9 ]
[ 611-08-5 ]

Reference： [1]American Chemical Journal,1905,vol. 34,p. 564

6
[ 7254-29-7 ]
[ 77994-12-8 ]

Reference： [1]Angewandte Chemie - International Edition,2007,vol. 46,p. 2478 - 2484
[2]Chemistry - An Asian Journal,2011,vol. 6,p. 1252 - 1262

7
[ 7254-29-7 ]
[ 108-24-7 ]
[ 3005-72-9 ]

Reference： [1]Chemistry - An Asian Journal,2011,vol. 6,p. 1252 - 1262

8
[ 7254-29-7 ]
[ 160948-35-6 ]

Yield	Reaction Conditions	Operation in experiment
	With trichlorophosphate; at 100℃; for 18.0h;Reflux;	Step 2-Synthesis of 6-chloro-5-nitro-1,6-dihydropyrimidin-2-amine A suspension mixture of <strong>[7254-29-7]2-amino-5-nitro-3,4-dihydropyrimidin-4-one</strong> (1.5 g, 9.61 mmol) and phosphorus oxychloride (27 mL, 0.29 mol) was heated under reflux (100 C.) for 18 hr. The reaction mixture turned into a yellow solution. The mixture was cooled to RT before being concentrated in vacuo. DCM (10 mL) was added and concentrated in vacuo was repeated. Ice (ca 5 g) was added, resulted in a sticky solid. DCM (20 mL) was added and the mixture was quenched by addition to an ice-cold saturated aqueous NaHCO3 solution (150 mL). The pH of mixture was adjusted to basic by final addition of 2M aq K2CO3. Attempt to extract product with DCM resulted in emulsion formation. Emulsion was removed by suction filtration. The aqueous layer was extracted with EtOAc (3*50 mL). The EtOAc extracts were combined with the DCM extract, dried over Na2SO4, filtered and concentrated in vacuo to afford the title compound as a yellow powder: 1H NMR (500 MHz, DMSO) delta 8.40-8.48 (2H, m), 9.02 (1H, s). LC-MS: m/z=+174.9 (M+H)+.

Reference： [1]Patent: US2012/214762,2012,A1 .Location in patent: Page/Page column 80

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Isomers

Technical Information

• 1,4-Addition of an Amine to a Conjugated Enone • 1,4-Addition of an Amine to a Conjugated Enone • Acyl Group Substitution • Amide Hydrolysis • Amide Hydrolysis • Amides Can Be Converted into Aldehydes • Amine Synthesis from Nitriles • Amine Synthesis from Nitriles • Amines Convert Acyl Chlorides into Amides • Amines Convert Esters into Amides • Azide Reduction by LiAlH4 • Azide Reduction by LiAlH4 • Basicity of Amines • Buchwald-Hartwig C-N Bond and C-O Bond Formation Reactions • Chan-Lam Coupling Reaction • Chichibabin Reaction • Complex Metal Hydride Reductions • Diazotization Reaction • DIBAL Attack Nitriles to Give Ketones • Enamine Formation • Formation of an Amide from an Amine and a Carboxylic Acid • Formation of an Amide from an Amine and a Carboxylic Acid • Hemiaminal Formation from Amines and Aldehydes or Ketones • Hemiaminal Formation from Amines and Aldehydes or Ketones • Hofmann Elimination • Hofmann Rearrangement • Hydride Reductions • Hydrolysis of Imines to Aldehydes and Ketones • Imine Formation from Amines and Aldehydes or Ketones • Lawesson's Reagent • Leuckart-Wallach Reaction • Mannich Reaction • Methylation of Ammonia • Methylation of Ammonia • Nitrosation of Amines • Peptide Bond Formation with DCC • Petasis Reaction • Preparation of Amines • Preparation of LDA • Reactions of Amines • Reduction of an Amide to an Amine • Reduction of an Amide to an Amine • Reductive Amination • Reductive Amination • Ring Opening of Azacyclopropanes • Ring Opening of Azacyclopropanes • Ring Opening of Oxacyclobutanes • Specialized Acylation Reagents-Carbodiimides and Related Reagents • Specialized Acylation Reagents-Ketenes • Specialized Acylation Reagents-Vilsmeier Reagent • Strecker Synthesis • Synthesis of 2-Amino Nitriles • Ugi Reaction

Historical Records

Related Functional Groups of
[ 7254-29-7 ]

Amides

[ 4214-85-1 ]

2-Amino-6-methyl-5-nitro-3H-pyrimidin-4-one

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[ 1672-50-0 ]

4,5-Diamino-6-hydroxypyrimidine

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[ 108-53-2 ]

2-Aminopyrimidin-4(1H)-one

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[ 611-08-5 ]

5-Nitropyrimidine-2,4(1H,3H)-dione

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[ 16632-21-6 ]

5-Nitro-6-methyluracil

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Amines

[ 4214-85-1 ]

2-Amino-6-methyl-5-nitro-3H-pyrimidin-4-one

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[ 1672-50-0 ]

4,5-Diamino-6-hydroxypyrimidine

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[ 108-53-2 ]

2-Aminopyrimidin-4(1H)-one

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[ 6232-92-4 ]

6-Nitro-1H-benzo[d]imidazol-2-amine

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[ 3346-22-3 ]

6-Amino-5-nitropyrimidine-2,4(1H,3H)-dione

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Nitroes

[ 4214-85-1 ]

2-Amino-6-methyl-5-nitro-3H-pyrimidin-4-one

Similarity: 0.90

[ 611-08-5 ]

5-Nitropyrimidine-2,4(1H,3H)-dione

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[ 16632-21-6 ]

5-Nitro-6-methyluracil

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[ 6232-92-4 ]

6-Nitro-1H-benzo[d]imidazol-2-amine

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[ 3346-22-3 ]

6-Amino-5-nitropyrimidine-2,4(1H,3H)-dione

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Related Parent Nucleus of
[ 7254-29-7 ]

Pyrimidines

[ 4214-85-1 ]

2-Amino-6-methyl-5-nitro-3H-pyrimidin-4-one

Similarity: 0.90

[ 1672-50-0 ]

4,5-Diamino-6-hydroxypyrimidine

Similarity: 0.66

[ 108-53-2 ]

2-Aminopyrimidin-4(1H)-one

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5-Nitropyrimidine-2,4(1H,3H)-dione

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[ 16632-21-6 ]

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Code	Phrase
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Code	Phrase
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P220	Keep/Store away from clothing/combustible materials.
P221	Take any precaution to avoid mixing with combustibles
P222	Do not allow contact with air.
P223	Keep away from any possible contact with water, because of violent reaction and possible flash fire.
P230	Keep wetted
P231	Handle under inert gas.
P232	Protect from moisture.
P233	Keep container tightly closed.
P234	Keep only in original container.
P235	Keep cool
P240	Ground/bond container and receiving equipment.
P241	Use explosion-proof electrical/ventilating/lighting/equipment.
P242	Use only non-sparking tools.
P243	Take precautionary measures against static discharge.
P244	Keep reduction valves free from grease and oil.
P250	Do not subject to grinding/shock/friction.
P251	Pressurized container: Do not pierce or burn, even after use.
P260	Do not breathe dust/fume/gas/mist/vapours/spray.
P261	Avoid breathing dust/fume/gas/mist/vapours/spray.
P262	Do not get in eyes, on skin, or on clothing.
P263	Avoid contact during pregnancy/while nursing.
P264	Wash hands thoroughly after handling.
P265	Wash skin thouroughly after handling.
P270	Do not eat, drink or smoke when using this product.
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P285	In case of inadequate ventilation wear respiratory protection.
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Response
Code	Phrase
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P315	Get immediate medical advice/attention.
P320
P302 + P352	IF ON SKIN: wash with plenty of soap and water.
P321
P322
P330	Rinse mouth.
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P342	If experiencing respiratory symptoms:
P350	Gently wash with plenty of soap and water.
P351	Rinse cautiously with water for several minutes.
P352	Wash with plenty of soap and water.
P353	Rinse skin with water/shower.
P360	Rinse immediately contaminated clothing and skin with plenty of water before removing clothes.
P361	Remove/Take off immediately all contaminated clothing.
P362	Take off contaminated clothing and wash before reuse.
P363	Wash contaminated clothing before reuse.
P370	In case of fire:
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P372	Explosion risk in case of fire.
P373	DO NOT fight fire when fire reaches explosives.
P374	Fight fire with normal precautions from a reasonable distance.
P376	Stop leak if safe to do so. Oxidising gases (section 2.4) 1
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P378
P380	Evacuate area.
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P390	Absorb spillage to prevent material damage.
P391	Collect spillage. Hazardous to the aquatic environment
P301 + P310	IF SWALLOWED: Immediately call a POISON CENTER or doctor/physician.
P301 + P312	IF SWALLOWED: call a POISON CENTER or doctor/physician IF you feel unwell.
P301 + P330 + P331	IF SWALLOWED: Rinse mouth. Do NOT induce vomiting.
P302 + P334	IF ON SKIN: Immerse in cool water/wrap in wet bandages.
P302 + P350	IF ON SKIN: Gently wash with plenty of soap and water.
P303 + P361 + P353	IF ON SKIN (or hair): Remove/Take off Immediately all contaminated clothing. Rinse SKIN with water/shower.
P304 + P312	IF INHALED: Call a POISON CENTER or doctor/physician if you feel unwell.
P304 + P340	IF INHALED: Remove victim to fresh air and Keep at rest in a position comfortable for breathing.
P304 + P341	IF INHALED: If breathing is difficult, remove victim to fresh air and keep at rest in a position comfortable for breathing.
P305 + P351 + P338	IF IN EYES: Rinse cautiously with water for several minutes. Remove contact lenses, if present and easy to do. Continue rinsing.
P306 + P360	IF ON CLOTHING: Rinse Immediately contaminated CLOTHING and SKIN with plenty of water before removing clothes.
P307 + P311	IF exposed: call a POISON CENTER or doctor/physician.
P308 + P313	IF exposed or concerned: Get medical advice/attention.
P309 + P311	IF exposed or if you feel unwell: call a POISON CENTER or doctor/physician.
P332 + P313	IF SKIN irritation occurs: Get medical advice/attention.
P333 + P313	IF SKIN irritation or rash occurs: Get medical advice/attention.
P335 + P334	Brush off loose particles from skin. Immerse in cool water/wrap in wet bandages.
P337 + P313	IF eye irritation persists: Get medical advice/attention.
P342 + P311	IF experiencing respiratory symptoms: call a POISON CENTER or doctor/physician.
P370 + P376	In case of fire: Stop leak if safe to Do so.
P370 + P378	In case of fire:
P370 + P380	In case of fire: Evacuate area.
P370 + P380 + P375	In case of fire: Evacuate area. Fight fire remotely due to the risk of explosion.
P371 + P380 + P375	In case of major fire and large quantities: Evacuate area. Fight fire remotely due to the risk of explosion.
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P401
P402	Store in a dry place.
P403	Store in a well-ventilated place.
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P411
P412	Do not expose to temperatures exceeding 50 oC/ 122 oF.
P413
P420	Store away from other materials.
P422
P402 + P404	Store in a dry place. Store in a closed container.
P403 + P233	Store in a well-ventilated place. Keep container tightly closed.
P403 + P235	Store in a well-ventilated place. Keep cool.
P410 + P403	Protect from sunlight. Store in a well-ventilated place.
P410 + P412	Protect from sunlight. Do not expose to temperatures exceeding 50 oC/122oF.
P411 + P235	Keep cool.
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P501	Dispose of contents/container to ...
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Physical hazards
Code	Phrase
H200	Unstable explosive
H201	Explosive; mass explosion hazard
H202	Explosive; severe projection hazard
H203	Explosive; fire, blast or projection hazard
H204	Fire or projection hazard
H205	May mass explode in fire
H220	Extremely flammable gas
H221	Flammable gas
H222	Extremely flammable aerosol
H223	Flammable aerosol
H224	Extremely flammable liquid and vapour
H225	Highly flammable liquid and vapour
H226	Flammable liquid and vapour
H227	Combustible liquid
H228	Flammable solid
H229	Pressurized container: may burst if heated
H230	May react explosively even in the absence of air
H231	May react explosively even in the absence of air at elevated pressure and/or temperature
H240	Heating may cause an explosion
H241	Heating may cause a fire or explosion
H242	Heating may cause a fire
H250	Catches fire spontaneously if exposed to air
H251	Self-heating; may catch fire
H252	Self-heating in large quantities; may catch fire
H260	In contact with water releases flammable gases which may ignite spontaneously
H261	In contact with water releases flammable gas
H270	May cause or intensify fire; oxidizer
H271	May cause fire or explosion; strong oxidizer
H272	May intensify fire; oxidizer
H280	Contains gas under pressure; may explode if heated
H281	Contains refrigerated gas; may cause cryogenic burns or injury
H290	May be corrosive to metals
Health hazards
Code	Phrase
H300	Fatal if swallowed
H301	Toxic if swallowed
H302	Harmful if swallowed
H303	May be harmful if swallowed
H304	May be fatal if swallowed and enters airways
H305	May be harmful if swallowed and enters airways
H310	Fatal in contact with skin
H311	Toxic in contact with skin
H312	Harmful in contact with skin
H313	May be harmful in contact with skin
H314	Causes severe skin burns and eye damage
H315	Causes skin irritation
H316	Causes mild skin irritation
H317	May cause an allergic skin reaction
H318	Causes serious eye damage
H319	Causes serious eye irritation
H320	Causes eye irritation
H330	Fatal if inhaled
H331	Toxic if inhaled
H332	Harmful if inhaled
H333	May be harmful if inhaled
H334	May cause allergy or asthma symptoms or breathing difficulties if inhaled
H335	May cause respiratory irritation
H336	May cause drowsiness or dizziness
H340	May cause genetic defects
H341	Suspected of causing genetic defects
H350	May cause cancer
H351	Suspected of causing cancer
H360	May damage fertility or the unborn child
H361	Suspected of damaging fertility or the unborn child
H361d	Suspected of damaging the unborn child
H362	May cause harm to breast-fed children
H370	Causes damage to organs
H371	May cause damage to organs
H372	Causes damage to organs through prolonged or repeated exposure
H373	May cause damage to organs through prolonged or repeated exposure
Environmental hazards
Code	Phrase
H400	Very toxic to aquatic life
H401	Toxic to aquatic life
H402	Harmful to aquatic life
H410	Very toxic to aquatic life with long-lasting effects
H411	Toxic to aquatic life with long-lasting effects
H412	Harmful to aquatic life with long-lasting effects
H413	May cause long-lasting harmful effects to aquatic life
H420	Harms public health and the environment by destroying ozone in the upper atmosphere

[ CAS No. 7254-29-7 ] {[proInfo.proName]}

Quality Control of [ 7254-29-7 ]

Related Doc. of [ 7254-29-7 ]

Product Details of [ 7254-29-7 ]

Calculated chemistry of [ 7254-29-7 ] Expand+

Physicochemical Properties

Pharmacokinetics

Lipophilicity

Druglikeness

Water Solubility

Medicinal Chemistry

Safety of [ 7254-29-7 ]

Application In Synthesis of [ 7254-29-7 ]

[ 7254-29-7 ] Synthesis Path-Upstream 1~4

[ 7254-29-7 ] Synthesis Path-Downstream 1~8

Technical Information

Related Functional Groups of [ 7254-29-7 ]

Amides

Amines

Nitroes

Related Parent Nucleus of [ 7254-29-7 ]

Pyrimidines

Precautionary Statements-General

Prevention

Response

Storage

Disposal

Physical hazards

Health hazards

Environmental hazards

Inquiry

Related Functional Groups of
[ 7254-29-7 ]

Related Parent Nucleus of
[ 7254-29-7 ]