1616761-01-3|(3R,4R)-4-Methyl-3-(methyl-7H-pyrrolo[2,3-d]pyrimidin-4-ylamino)-beta-oxo-1-piperidinepropanoic acid methyl ester

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(3R,4R)-4-Methyl-3-(methyl-7H-pyrrolo[2,3-d]pyrimidin-4-ylamino)-beta-oxo-1-piperidinepropanoic acid methyl ester | CAS:1616761-01-3

(3R,4R)-4-Methyl-3-(methyl-7H-pyrrolo[2,3-d]pyrimidin-4-ylamino)-beta-oxo-1-piperidinepropanoic acid methyl ester

Name：(3R,4R)-4-Methyl-3-(methyl-7H-pyrrolo[2,3-d]pyrimidin-4-ylamino)-beta-oxo-1-piperidinepropanoic acid methyl ester
CAS：1616761-01-3
Synonyms：
Molecular Formula：C₁₇H₂₃N₅O₃
Molecular Weight：345.40
EINESC：

Description

Properties

Density	1.290±0.06 g/cm3 (20 º

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Peer-Reviewed Papers

Structure-activity relationships in the destruction of cytochrome P-450 mediated by certain ethynyl-substituted compounds in rats.I N White Biochemical pharmacology, 29(24), 3253-3255 (1980-12-01) Hydroboration. 50. Hydroboration of representative alkynes with 9-borabicyclo [3.3.1] nonane-a simple synthesis of versatile vinyl bora and gem-dibora intermediates.Brown HC, et al. Journal of the American Chemical Society, 101(1), 96-99 (1979) Highly selective and practical alkyne-alkyne cross-coupling using Cp2ZrBu2 and ethylene.Xi Z, et al. The Journal of Organic Chemistry, 60(14), 4444-4448 (1995) Reduction of organic compounds by lithium in low molecular weight amines. II. Stereochemistry. Chemical reduction of an isolated non-terminal double bond.Benkeser RA, et al. Journal of the American Chemical Society, 77(12), 3378-3379 (1955)

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