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CAS No.: | 1202044-20-9 |
---|---|
Name: | Ostarine(MK-2866) |
Article Data: | 1 |
Molecular Structure: | |
Formula: | C19H14F3N3O3 |
Molecular Weight: | 393.302 |
Synonyms: | MK-2866;(2S)-3-(4-Cyanophenoxy-2,3,5,6-d4)-N-[4-cyano-3-(trifluoromethyl)phenyl]-2-hydroxy-2-methylpropanamide; |
Density: | 1.418 g/cm3 |
Melting Point: | 70–74 °C (158–165 °F) |
Boiling Point: | 632.261 °C at 760 mmHg |
Flash Point: | 336.18 °C |
PSA: | 106.14000 |
LogP: | 3.29026 |
4-cyanophenol-d4
(2R)-3-bromo-N-[4-cyano-3-(trifluoromethyl)phenyl]-2-hydroxy-2-methylpropanamide
(S)-N-(4-cyano-3-(trifluoromethyl)phenyl)-3-(4-cyanophenoxy)-2-hydroxy-2-methylpropanamide-d4
Conditions | Yield |
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With sodium carbonate In acetone for 3h; Reflux; | 59.9% |
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The MK-2866, with the CAS registry number 1202044-20-9, is also known as GTx-024, MK-2866. This chemical's molecular formula is C19H14F3N3O3 and molecular weight is 389.328. Its systematic name is called (2R)-3-(4-cyanophenoxy)-N-[4-cyano-3-(trifluoromethyl)phenyl]-2-hydroxy-2-methyl-propanamide. MK-2866 is an investigational selective androgen receptor modulator (SARM) from GTx Inx.
Physical properties of MK-2866: (1)ACD/LogP: 4.21; (2)ACD/LogD (pH 5.5): 4.21; (3)ACD/LogD (pH 7.4): 4.21; (4)ACD/BCF (pH 5.5): 932.123; (5)ACD/BCF (pH 7.4): 932.097; (6)ACD/KOC (pH 5.5): 4646.75; (7)ACD/KOC (pH 7.4): 4646.62; (8)#H bond acceptors: 6; (9)#H bond donors: 2; (10)#Freely Rotating Bonds: 6; (11)Index of Refraction: 1.578; (12)Molar Refractivity: 91.16 cm3; (13)Molar Volume: 274.531 cm3; (14)Surface Tension: 59.378 dyne/cm; (15)Density: 1.418 g/cm3; (16)Flash Point: 336.18 °C; (17)Enthalpy of Vaporization: 98.261 kJ/mol; (18)Boiling Point: 632.261 °C at 760 mmHg; (19)Vapour Pressure: 0 mmHg at 25°C.
You can still convert the following datas into molecular structure:
(1)SMILES: C[C@@](COc1ccc(cc1)C#N)(C(=O)Nc2ccc(c(c2)C(F)(F)F)C#N)O
(2)InChI: InChI=1/C19H14F3N3O3/c1-18(27,11-28-15-6-2-12(9-23)3-7-15)17(26)25-14-5-4-13(10-24)16(8-14)19(20,21)22/h2-8,27H,11H2,1H3,(H,25,26)/t18-/m1/s1
(3)InChIKey: JNGVJMBLXIUVRD-GOSISDBHBL