Cas 1137150-74-3,1-[(1S)-2-methoxy-2-oxo-1-phenylethyl] 4-methyl (2R)-2-hydroxy-2-(3-methylbut-2-en-1-yl)butanedioate

1137150-74-3

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Basic information

Product Name: 1-[(1S)-2-methoxy-2-oxo-1-phenylethyl] 4-methyl (2R)-2-hydroxy-2-(3-methylbut-2-en-1-yl)butanedioate
Synonyms: 1-[(1S)-2-methoxy-2-oxo-1-phenylethyl] 4-methyl (2R)-2-hydroxy-2-(3-methylbut-2-en-1-yl)butanedioate
CAS NO:1137150-74-3
Molecular Formula:
Molecular Weight: 364.395
EINECS: N/A
Product Categories: N/A
Mol File: 1137150-74-3.mol
Article Data: 1

Chemical Properties

Melting Point: N/A
Boiling Point: N/A
Flash Point: N/A
Appearance: N/A
Density: N/A
Refractive Index: N/A
Storage Temp.: N/A
Solubility: N/A
CAS DataBase Reference: 1-[(1S)-2-methoxy-2-oxo-1-phenylethyl] 4-methyl (2R)-2-hydroxy-2-(3-methylbut-2-en-1-yl)butanedioate(CAS DataBase Reference)
NIST Chemistry Reference: 1-[(1S)-2-methoxy-2-oxo-1-phenylethyl] 4-methyl (2R)-2-hydroxy-2-(3-methylbut-2-en-1-yl)butanedioate(1137150-74-3)
EPA Substance Registry System: 1-[(1S)-2-methoxy-2-oxo-1-phenylethyl] 4-methyl (2R)-2-hydroxy-2-(3-methylbut-2-en-1-yl)butanedioate(1137150-74-3)

Safety Data

Hazard Codes: N/A
Statements: N/A
Safety Statements: N/A
WGK Germany:
RTECS:
HazardClass: N/A
PackingGroup: N/A
Hazardous Substances Data: 1137150-74-3(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1137150-74-3 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,1,3,7,1,5 and 0 respectively; the second part has 2 digits, 7 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 1137150-74:
(9*1)+(8*1)+(7*3)+(6*7)+(5*1)+(4*5)+(3*0)+(2*7)+(1*4)=123
123 % 10 = 3
So 1137150-74-3 is a valid CAS Registry Number.

1137150-74-3Upstream product

1137150-74-3Downstream Products

1137150-75-4 (1S)-2-methoxy-2-oxo-1-phenylethyl (2R)-2-(2-methoxy-2-oxoethyl)-5,5-dimethyltetrahydrofuran-2-carboxylate

1137150-74-3Relevant articles and documents

Synthesis of optically active monoacid side-chains of Cephalotaxus alkaloids

Berhal, Farouk,Tardy, Sebastien,Perard-Viret, Joelle,Royer, Jacques

experimental part, p. 437 - 443 (2009/06/18)

The general preparation of enantiopure monoacid side-chains of several esters of cephalotaxine is described. The strategy, similar to Weinreb's approach to the synthesis of deoxyharringtonine, used as key intermediate the chiral nonracemic epoxide 11a pre

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