Products Categories
CAS No.: | 477600-75-2 |
---|---|
Name: | 3-((3R,4R)-4-methyl-3-(methyl(7H-pyrrolo[2,3-d]pyrimidin-4-yl)amino)piperidin-1-yl)-3-oxopropanenitrile |
Molecular Structure: | |
Formula: | C16H20N6O |
Molecular Weight: | 312.37 |
Synonyms: | Tofacitinib;3-((3R,4R)-4-methyl-3-(methyl(7H-pyrrolo[2,3-d]pyrimidin-4-yl)amino)piperidin-1-yl)-3-oxopropanenitrile; |
EINECS: | 689-145-4 |
Density: | 1.296 g/cm3 |
Boiling Point: | 585.845 °C at 760 mmHg |
Flash Point: | 308.108 °C |
PSA: | 88.91000 |
LogP: | 1.48268 |
What can I do for you?
Get Best Price
Tofacitinib, with the CAS NO.477600-75-2, has the synonyms of 3-((3R,4R)-4-Methyl-3-(methyl(7H-pyrrolo(2,3-d)pyrimidin-4-yl)amino)piperidin-1-yl)-3-oxopropanenitrile; CP 690550; 3-Piperidinamine, 1-(cyanoacetyl)-4-methyl-N-methyl-N-1H-pyrrolo(2,3-d)pyrimidin-4-yl-, (3R,4R)-. Tofacitinib is a drug discovered and developed by Pfizer. Tofacitinib is a selective inhibitor of Janus kinase (JAK) enzymes. JAKs mediate signaling by surface receptors for several important cytokines that are fundamental to the propagation of inflammation in RA.
Physical properties about Tofacitinib are: (1)ACD/LogP: 0.925; (2)ACD/LogD (pH 5.5): -0.20; (3)ACD/LogD (pH 7.4): -0.79; (4)ACD/BCF (pH 5.5): 1.00; (5)ACD/BCF (pH 7.4): 1.00; (6)ACD/KOC (pH 5.5): 5.74; (7)ACD/KOC (pH 7.4): 1.45; (8)#H bond acceptors: 7; (9)#H bond donors: 1; (10)#Freely Rotating Bonds: 3; (11)Index of Refraction: 1.646; (12)Molar Refractivity: 87.474 cm3; (13)Molar Volume: 241.009 cm3; (14)Polarizability: 34.677 10-24cm3; (15)Surface Tension: 69.2720031738281 dyne/cm; (16)Density: 1.296 g/cm3; (17)Flash Point: 308.108 °C; (18)Enthalpy of Vaporization: 87.509 kJ/mol; (19)Boiling Point: 585.845 °C at 760 mmHg
You can still convert the following datas into molecular structure:
(1)InChI=1S/C16H20N6O/c1-11-5-8-22(14(23)3-6-17)9-13(11)21(2)16-12-4-7-18-15(12)19-10-20-16/h4,7,10-11,13H,3,5,8-9H2,1-2H3,(H,18,19,20)/t11-,13+/m1/s1;
(2)InChIKey=UJLAWZDWDVHWOW-YPMHNXCESA-N;
(3)Smiles[C@@H]1([C@H](CN(CC1)C(=O)CC#N)N(c1ncnc2[nH]ccc12)C)C