Home Cart 0 Sign in  
X

[ CAS No. 5472-46-8 ] {[proInfo.proName]}

,{[proInfo.pro_purity]}
Cat. No.: {[proInfo.prAm]}
3d Animation Molecule Structure of 5472-46-8
Chemical Structure| 5472-46-8
Chemical Structure| 5472-46-8
Structure of 5472-46-8 * Storage: {[proInfo.prStorage]}
Cart0 Add to My Favorites Add to My Favorites Bulk Inquiry Inquiry Add To Cart

Quality Control of [ 5472-46-8 ]

Related Doc. of [ 5472-46-8 ]

Alternatived Products of [ 5472-46-8 ]

Product Details of [ 5472-46-8 ]

CAS No. :5472-46-8 MDL No. :MFCD05721220
Formula : C8H11N3O2 Boiling Point : -
Linear Structure Formula :- InChI Key :YRKLYFMSXXRRNJ-UHFFFAOYSA-N
M.W : 181.19 Pubchem ID :231662
Synonyms :

Calculated chemistry of [ 5472-46-8 ]

Physicochemical Properties

Num. heavy atoms : 13
Num. arom. heavy atoms : 6
Fraction Csp3 : 0.38
Num. rotatable bonds : 3
Num. H-bond acceptors : 4.0
Num. H-bond donors : 1.0
Molar Refractivity : 47.49
TPSA : 78.1 Ų

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) : -6.67 cm/s

Lipophilicity

Log Po/w (iLOGP) : 1.8
Log Po/w (XLOGP3) : 1.03
Log Po/w (WLOGP) : 0.55
Log Po/w (MLOGP) : 0.06
Log Po/w (SILICOS-IT) : 0.78
Consensus Log Po/w : 0.84

Druglikeness

Lipinski : 0.0
Ghose : None
Veber : 0.0
Egan : 0.0
Muegge : 1.0
Bioavailability Score : 0.55

Water Solubility

Log S (ESOL) : -1.76
Solubility : 3.18 mg/ml ; 0.0175 mol/l
Class : Very soluble
Log S (Ali) : -2.26
Solubility : 0.995 mg/ml ; 0.00549 mol/l
Class : Soluble
Log S (SILICOS-IT) : -2.16
Solubility : 1.25 mg/ml ; 0.0069 mol/l
Class : Soluble

Medicinal Chemistry

PAINS : 0.0 alert
Brenk : 0.0 alert
Leadlikeness : 1.0
Synthetic accessibility : 1.85

Safety of [ 5472-46-8 ]

Signal Word:Warning Class:N/A
Precautionary Statements:P305+P351+P338 UN#:N/A
Hazard Statements:H302-H319 Packing Group:N/A
GHS Pictogram:

Application In Synthesis of [ 5472-46-8 ]

* 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 [ 5472-46-8 ]
  • Downstream synthetic route of [ 5472-46-8 ]

[ 5472-46-8 ] Synthesis Path-Upstream   1~10

  • 1
  • [ 42466-67-1 ]
  • [ 143-37-3 ]
  • [ 27058-54-4 ]
  • [ 5472-46-8 ]
Reference: [1] Chemical and Pharmaceutical Bulletin, 1970, vol. 18, p. 1003 - 1007
[2] Chemische Berichte, 1941, vol. 74, p. 1126
  • 2
  • [ 5472-46-8 ]
  • [ 73-67-6 ]
Reference: [1] Chemische Berichte, 1953, vol. 86, p. 1404,1406
[2] Trudy vitamin.Inst., 1953, vol. 4, p. 20,22[3] Chem.Abstr., 1956, p. 4156
  • 3
  • [ 698-29-3 ]
  • [ 5472-46-8 ]
Reference: [1] Journal of the American Chemical Society, 1940, vol. 62, p. 2818
  • 4
  • [ 769-52-8 ]
  • [ 64-17-5 ]
  • [ 5472-46-8 ]
Reference: [1] Journal of the American Chemical Society, 1940, vol. 62, p. 2818
  • 5
  • [ 2134-36-3 ]
  • [ 5472-46-8 ]
Reference: [1] Chemische Berichte, 1953, vol. 86, p. 1404,1406
[2] Journal of the Chemical Society, 1937, p. 367[3] Journal of the Chemical Society, 1938, p. 28
  • 6
  • [ 42466-67-1 ]
  • [ 143-37-3 ]
  • [ 27058-54-4 ]
  • [ 5472-46-8 ]
Reference: [1] Chemical and Pharmaceutical Bulletin, 1970, vol. 18, p. 1003 - 1007
[2] Chemische Berichte, 1941, vol. 74, p. 1126
  • 7
  • [ 53135-24-3 ]
  • [ 5472-46-8 ]
Reference: [1] Journal of the Chemical Society, 1937, p. 367[2] Journal of the Chemical Society, 1938, p. 28
  • 8
  • [ 87-13-8 ]
  • [ 5472-46-8 ]
Reference: [1] Journal of the Chemical Society, 1937, p. 367[2] Journal of the Chemical Society, 1938, p. 28
  • 9
  • [ 38109-77-2 ]
  • [ 1000-84-6 ]
  • [ 5472-46-8 ]
Reference: [1] Patent: US2235638, 1937, ,
[2] Fortschr. Teerfarbenfabr. Verw. Industriezweige, vol. 25, p. 432
[3] Fortschr. Teerfarbenfabr. Verw. Industriezweige, vol. 25, p. 432,434
[4] Patent: US2235638, 1937, ,
  • 10
  • [ 38109-77-2 ]
  • [ 62-55-5 ]
  • [ 5472-46-8 ]
Reference: [1] Journal of the Chemical Society, 1943, p. 388
[2] Patent: US2271503, 1940, ,
[3] DRP/DRBP Org.Chem.,
Same Skeleton Products
Historical Records

Related Functional Groups of
[ 5472-46-8 ]

Esters

Chemical Structure| 65195-35-9

[ 65195-35-9 ]

Ethyl 4-aminopyrimidine-5-carboxylate

Similarity: 0.93

Chemical Structure| 714975-53-8

[ 714975-53-8 ]

Methyl 4-aminopyrimidine-5-carboxylate

Similarity: 0.90

Chemical Structure| 15400-54-1

[ 15400-54-1 ]

Ethyl 2,4-diaminopyrimidine-5-carboxylate

Similarity: 0.89

Chemical Structure| 27058-46-4

[ 27058-46-4 ]

Ethyl 4-amino-2-phenylpyrimidine-5-carboxylate

Similarity: 0.87

Chemical Structure| 20187-46-6

[ 20187-46-6 ]

Ethyl 4-amino-2-hydroxypyrimidine-5-carboxylate

Similarity: 0.86

Amines

Chemical Structure| 65195-35-9

[ 65195-35-9 ]

Ethyl 4-aminopyrimidine-5-carboxylate

Similarity: 0.93

Chemical Structure| 714975-53-8

[ 714975-53-8 ]

Methyl 4-aminopyrimidine-5-carboxylate

Similarity: 0.90

Chemical Structure| 15400-54-1

[ 15400-54-1 ]

Ethyl 2,4-diaminopyrimidine-5-carboxylate

Similarity: 0.89

Chemical Structure| 769-52-8

[ 769-52-8 ]

4-Amino-2-methylpyrimidine-5-carboxylic acid

Similarity: 0.88

Chemical Structure| 27058-46-4

[ 27058-46-4 ]

Ethyl 4-amino-2-phenylpyrimidine-5-carboxylate

Similarity: 0.87

Related Parent Nucleus of
[ 5472-46-8 ]

Pyrimidines

Chemical Structure| 65195-35-9

[ 65195-35-9 ]

Ethyl 4-aminopyrimidine-5-carboxylate

Similarity: 0.93

Chemical Structure| 714975-53-8

[ 714975-53-8 ]

Methyl 4-aminopyrimidine-5-carboxylate

Similarity: 0.90

Chemical Structure| 15400-54-1

[ 15400-54-1 ]

Ethyl 2,4-diaminopyrimidine-5-carboxylate

Similarity: 0.89

Chemical Structure| 769-52-8

[ 769-52-8 ]

4-Amino-2-methylpyrimidine-5-carboxylic acid

Similarity: 0.88

Chemical Structure| 27058-46-4

[ 27058-46-4 ]

Ethyl 4-amino-2-phenylpyrimidine-5-carboxylate

Similarity: 0.87