[ CAS No. 105618-29-9 ] {[proInfo.proName]}

Name: 105618-29-9|Furo[3,4-b]furo[3',4':5,6]pyrazino[2,3-f]furo[3',4':5,6]pyrazino[2,3-h]quinoxaline-1,3,6,8,11,13-hexaone|95%
Brand: Ambeed
SKU: A1494920
Rating: 99 (30 reviews)

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Quality Control of [ 105618-29-9 ]

COA NMR CNMR HPLC LC-MS

Related Doc. of [ 105618-29-9 ]

SDS Specification

Alternatived Products of [ 105618-29-9 ]

Product Details of [ 105618-29-9 ]

CAS No. :	105618-29-9	MDL No. :	N/A
Formula :	C₁₈N₆O₉	Boiling Point :	-
Linear Structure Formula :	-	InChI Key :	BTASSOQNDRGAGE-UHFFFAOYSA-N
M.W :	444.23	Pubchem ID :	13692981
Synonyms :

Safety of [ 105618-29-9 ]

Signal Word:	Warning	Class:	N/A
Precautionary Statements:	P261-P280-P301+P312-P302+P352-P305+P351+P338	UN#:	N/A
Hazard Statements:	H302-H315-H319-H335	Packing Group:	N/A
GHS Pictogram:

Application In Synthesis of [ 105618-29-9 ]

* 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.

Downstream synthetic route of [ 105618-29-9 ]

[ 105618-29-9 ] Synthesis Path-Downstream 1~18

1
[ 67-56-1 ]
[ 105618-29-9 ]
[ 120933-46-2 ]

Yield	Reaction Conditions	Operation in experiment
	Yield given;

Reference： [1]Kanakarajan, K.; Czarnik, Anthony W. [Journal of Heterocyclic Chemistry, 1988, vol. 25, p. 1869 - 1872]

2
[ 111-26-2 ]
[ 105618-29-9 ]
[ 120933-47-3 ]

Yield	Reaction Conditions	Operation in experiment
88%	In acetonitrile

Reference： [1]Kanakarajan, K.; Czarnik, Anthony W. [Journal of Heterocyclic Chemistry, 1988, vol. 25, p. 1869 - 1872]

3
[ 771-60-8 ]
[ 105618-29-9 ]
[ 120933-57-5 ]

Yield	Reaction Conditions	Operation in experiment
	In N,N-dimethyl acetamide for 0.25h; Heating;

Reference： [1]Kanakarajan, K.; Czarnik, Anthony W. [Journal of Heterocyclic Chemistry, 1988, vol. 25, p. 1869 - 1872]

4
[ 769-92-6 ]
[ 105618-29-9 ]
C₄₈H₃₉N₉O₆ [ No CAS ]

Yield	Reaction Conditions	Operation in experiment
	With trifluoroacetic anhydride

Reference： [1]Rademacher, Jude T.; Czarnik, Anthony W. [Journal of the American Chemical Society, 1993, vol. 115, # 7, p. 3018 - 3019]

5
[ 769-92-6 ]
[ 105618-29-9 ]
3,7,10-Tris-(4-tert-butyl-phenylcarbamoyl)-1,4,5,8,9,12-hexaaza-triphenylene-2,6,11-tricarboxylic acid [ No CAS ]
3,7,11-Tris-(4-tert-butyl-phenylcarbamoyl)-1,4,5,8,9,12-hexaaza-triphenylene-2,6,10-tricarboxylic acid [ No CAS ]

Yield	Reaction Conditions	Operation in experiment
	Title compound not separated from byproducts;

Reference： [1]Rademacher, Jude T.; Czarnik, Anthony W. [Journal of the American Chemical Society, 1993, vol. 115, # 7, p. 3018 - 3019]

6
[ 105598-29-6 ]
[ 105618-29-9 ]

Yield	Reaction Conditions	Operation in experiment
95%	With acetic anhydride at 115℃; for 0.166667h;
	With acetic anhydride at 115℃;
	With acetic anhydride at 115 - 117℃; for 0.333333h; Inert atmosphere;

Reference： [1]Kanakarajan, K.; Czarnik, Anthony W. [Journal of Organic Chemistry, 1986, vol. 51, # 26, p. 5241 - 5243]
[2]Kanakarajan, K.; Czarnik, Anthony W. [Journal of Heterocyclic Chemistry, 1988, vol. 25, p. 1869 - 1872]
[3]Bhanvadia, Viraj J.; Patel, Arun L.; Zade, Sanjio S. [New Journal of Chemistry, 2018, vol. 42, # 21, p. 17700 - 17707]

7
[ 105618-29-9 ]
[ 124-40-3 ]
[ 120933-52-0 ]

Yield	Reaction Conditions	Operation in experiment
	In acetonitrile

Reference： [1]Kanakarajan, K.; Czarnik, Anthony W. [Journal of Heterocyclic Chemistry, 1988, vol. 25, p. 1869 - 1872]

8
[ 105618-29-9 ]
[ 75-64-9 ]
[ 120933-58-6 ]

Yield	Reaction Conditions	Operation in experiment
	In acetonitrile for 1h;

Reference： [1]Kanakarajan, K.; Czarnik, Anthony W. [Journal of Heterocyclic Chemistry, 1988, vol. 25, p. 1869 - 1872]

9
[ 105618-29-9 ]
[ 120933-53-1 ]

Yield	Reaction Conditions	Operation in experiment
	Multi-step reaction with 2 steps 1: acetonitrile 2: thionyl chloride / 0.5 h / Heating

Reference： [1]Kanakarajan, K.; Czarnik, Anthony W. [Journal of Heterocyclic Chemistry, 1988, vol. 25, p. 1869 - 1872]

10
[ 105618-29-9 ]
[ 120933-50-8 ]

Yield	Reaction Conditions	Operation in experiment
	Multi-step reaction with 3 steps 1: acetonitrile 2: thionyl chloride / 0.5 h / Heating 3: 0.25 h

Reference： [1]Kanakarajan, K.; Czarnik, Anthony W. [Journal of Heterocyclic Chemistry, 1988, vol. 25, p. 1869 - 1872]

11
[ 105618-29-9 ]
[ 120933-51-9 ]

Yield	Reaction Conditions	Operation in experiment
	Multi-step reaction with 4 steps 1: acetonitrile 2: thionyl chloride / 0.5 h / Heating 3: 0.25 h 4: 60 percent / acetonitrile / 0.17 h / Heating

Reference： [1]Kanakarajan, K.; Czarnik, Anthony W. [Journal of Heterocyclic Chemistry, 1988, vol. 25, p. 1869 - 1872]

12
[ 105618-29-9 ]
[ 86723-23-1 ]
C₈₄H₁₀₈N₁₂O₉ [ No CAS ]

Yield	Reaction Conditions	Operation in experiment
7%	Stage #1: hexaazatriphenylenehexacarboxylic acid trianhydride; 4,5-bis(octyloxy)benzene-1,2-diamine With triethylamine In acetonitrile at 90℃; for 24h; Inert atmosphere; Stage #2: In 1-methyl-pyrrolidin-2-one at 190℃; for 30h;

Reference： [1]Bhanvadia, Viraj J.; Patel, Arun L.; Zade, Sanjio S. [New Journal of Chemistry, 2018, vol. 42, # 21, p. 17700 - 17707]

13
[ 105618-29-9 ]
[ 86723-23-1 ]
C₈₄H₁₀₈N₁₂O₉ [ No CAS ]
C₁₅₀H₂₂₂N₁₈O₁₂ [ No CAS ]

Yield	Reaction Conditions	Operation in experiment
	Stage #1: hexaazatriphenylenehexacarboxylic acid trianhydride; 4,5-bis(octyloxy)benzene-1,2-diamine With triethylamine In acetonitrile at 90℃; for 24h; Inert atmosphere; Stage #2: In 1-methyl-pyrrolidin-2-one at 190℃; for 30h;

Reference： [1]Bhanvadia, Viraj J.; Patel, Arun L.; Zade, Sanjio S. [New Journal of Chemistry, 2018, vol. 42, # 21, p. 17700 - 17707]

14
[ 527-31-1 ]
[ 105618-29-9 ]

Reference： [1]New Journal of Chemistry,2018,vol. 42,p. 17700 - 17707

15
[ 105598-27-4 ]
[ 105618-29-9 ]

Yield	Reaction Conditions	Operation in experiment
	Multi-step reaction with 3 steps 1.1: sulfuric acid / 72 h / 20 °C 2.1: acetic acid; sodium nitrite; trifluoroacetic acid / 12 h 2.2: 12 h / 20 °C 3.1: acetic anhydride / 0.33 h / 115 - 117 °C / Inert atmosphere

Reference： [1]Bhanvadia, Viraj J.; Patel, Arun L.; Zade, Sanjio S. [New Journal of Chemistry, 2018, vol. 42, # 21, p. 17700 - 17707]

16
[ 105598-28-5 ]
[ 105618-29-9 ]

Yield	Reaction Conditions	Operation in experiment
	Multi-step reaction with 2 steps 1.1: acetic acid; sodium nitrite; trifluoroacetic acid / 12 h 1.2: 12 h / 20 °C 2.1: acetic anhydride / 0.33 h / 115 - 117 °C / Inert atmosphere

Reference： [1]Bhanvadia, Viraj J.; Patel, Arun L.; Zade, Sanjio S. [New Journal of Chemistry, 2018, vol. 42, # 21, p. 17700 - 17707]

17
[ 105618-29-9 ]
[ 865606-43-5 ]

Yield	Reaction Conditions	Operation in experiment
89.3 %	With ammonium hydroxide at 20℃; Inert atmosphere;	1-7 Example 1 General procedure: Add 30ml of ammonia (28wt%) to a 100mL three-mouth flask, and at the same time add hexaazabenzophenanthrene hexacarboxylic acid trianhydride (purchased from Aneji) (0.444g, 1mmol), under the protection of nitrogen, the reaction mixture is subjected to uninterrupted magnetic stirring at room temperature, the reaction time is 6 hours, after the end of the reaction, vacuum filtration collects solids, washed with ethanol three times, and vacuum drying at 60 °C overnight to obtain compound A: hexaazabenzophanthrene hexaforminimide, with a yield of 85.8%.

Reference： [1]Current Patent Assignee: UNIV CHANGZHOU - CN116253738, 2023, A Location in patent: Paragraph 0010; 0067-0085

18
[ 1455-77-2 ]
[ 105618-29-9 ]
[ CAS Unavailable ]

Yield	Reaction Conditions	Operation in experiment
80.5 %	In N,N-dimethyl-formamide Inert atmosphere; Reflux;	8-13 Example 8 General procedure: Add 45 mL of anhydrous DMF to a 100 ml three-mouth flask and purge with nitrogen for 15 min while adding hexaazabenzophene hexacarboxylic acid trianhydride (0.444 g, 1 mmol) and 3,5-diamino-1,2,4-triazole (0.396 g, 4 mmol). In the whole process, under the protection of nitrogen, continuous stirring and heating reflux for 24 hours, then the heating device was removed to cool to room temperature, the solid product was precipitated through an ice water bath, the solids were collected by filtration, the filter cake was washed three times with ethanol, and vacuum dried to obtain compound B: tris(3-amino-1,2,4-triazolyl)hexaazabenzophenanthrene hexaformylimide with a yield of 75.2%.

Reference： [1]Current Patent Assignee: UNIV CHANGZHOU - CN116253738, 2023, A Location in patent: Paragraph 0010; 0086-0103

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[ 105618-29-9 ]

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Code	Phrase
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Prevention
Code	Phrase
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P222	Do not allow contact with air.
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Response
Code	Phrase
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P320
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P321
P322
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P337	If eye irritation persists:
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P341	If breathing is difficult, remove victim to fresh air and keep at rest in a position comfortable for breathing.
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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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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P391	Collect spillage. Hazardous to the aquatic environment
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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:
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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. 105618-29-9 ] {[proInfo.proName]}

Quality Control of [ 105618-29-9 ]

Related Doc. of [ 105618-29-9 ]

Product Details of [ 105618-29-9 ]

Safety of [ 105618-29-9 ]

Application In Synthesis of [ 105618-29-9 ]

[ 105618-29-9 ] Synthesis Path-Downstream 1~18

Related Parent Nucleus of [ 105618-29-9 ]

Pyrazines

Quinoxalines

Precautionary Statements-General

Prevention

Response

Storage

Disposal

Physical hazards

Health hazards

Environmental hazards

Inquiry

Related Parent Nucleus of
[ 105618-29-9 ]