Cas 135144-85-3,(Z)-(S)-2-Hydroxy-oct-3-enoic acid (1R,2S,5R)-5-methyl-2-(1-methyl-1-phenyl-ethyl)-cyclohexyl ester

135144-85-3

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Basic information

Product Name: (Z)-(S)-2-Hydroxy-oct-3-enoic acid (1R,2S,5R)-5-methyl-2-(1-methyl-1-phenyl-ethyl)-cyclohexyl ester
Synonyms: (Z)-(S)-2-Hydroxy-oct-3-enoic acid (1R,2S,5R)-5-methyl-2-(1-methyl-1-phenyl-ethyl)-cyclohexyl ester
CAS NO:135144-85-3
Molecular Formula:
Molecular Weight: 372.548
EINECS: N/A
Product Categories: N/A

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: (Z)-(S)-2-Hydroxy-oct-3-enoic acid (1R,2S,5R)-5-methyl-2-(1-methyl-1-phenyl-ethyl)-cyclohexyl ester(CAS DataBase Reference)
NIST Chemistry Reference: (Z)-(S)-2-Hydroxy-oct-3-enoic acid (1R,2S,5R)-5-methyl-2-(1-methyl-1-phenyl-ethyl)-cyclohexyl ester(135144-85-3)
EPA Substance Registry System: (Z)-(S)-2-Hydroxy-oct-3-enoic acid (1R,2S,5R)-5-methyl-2-(1-methyl-1-phenyl-ethyl)-cyclohexyl ester(135144-85-3)

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: 135144-85-3(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 135144-85-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,5,1,4 and 4 respectively; the second part has 2 digits, 8 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 135144-85:
(8*1)+(7*3)+(6*5)+(5*1)+(4*4)+(3*4)+(2*8)+(1*5)=113
113 % 10 = 3
So 135144-85-3 is a valid CAS Registry Number.

135144-85-3Upstream product

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135144-85-3Relevant academic research and scientific papers

A New Vinylsilane Substitution Reaction with Glyoxylate: Asymmetric Synthesis of α-Hydroxy β,γ-Unsaturated Esters

Mikami, Koichi,Wakabayashi, Hideaki,Nakai, Takeshi

, p. 4337 - 4339 (1991)

The vinylsilane substitution reaction with glyoxylate and the asymmetric version thereof are described.These new reactions provide α-hydroxy β,γ-unsaturated esters of biological and synthetic importance in high enantiomeric and geometric purity.

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