Cas 116760-75-9,(2R,3S)-4-Cyclohexyl-3-hydroxy-2-methyl-2-phenylsulfanyl-butyric acid methyl ester

116760-75-9

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Basic information

Product Name: (2R,3S)-4-Cyclohexyl-3-hydroxy-2-methyl-2-phenylsulfanyl-butyric acid methyl ester
Synonyms: (2R,3S)-4-Cyclohexyl-3-hydroxy-2-methyl-2-phenylsulfanyl-butyric acid methyl ester
CAS NO:116760-75-9
Molecular Formula:
Molecular Weight: 322.469
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: (2R,3S)-4-Cyclohexyl-3-hydroxy-2-methyl-2-phenylsulfanyl-butyric acid methyl ester(CAS DataBase Reference)
NIST Chemistry Reference: (2R,3S)-4-Cyclohexyl-3-hydroxy-2-methyl-2-phenylsulfanyl-butyric acid methyl ester(116760-75-9)
EPA Substance Registry System: (2R,3S)-4-Cyclohexyl-3-hydroxy-2-methyl-2-phenylsulfanyl-butyric acid methyl ester(116760-75-9)

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: 116760-75-9(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 116760-75-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,6,7,6 and 0 respectively; the second part has 2 digits, 7 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 116760-75:
(8*1)+(7*1)+(6*6)+(5*7)+(4*6)+(3*0)+(2*7)+(1*5)=129
129 % 10 = 9
So 116760-75-9 is a valid CAS Registry Number.

116760-75-9Upstream product

116760-66-8 4-Cyclohexyl-2-methyl-3-oxo-2-phenylsulfanyl-butyric acid methyl ester

116760-75-9Downstream Products

116760-75-9Relevant academic research and scientific papers

A STEREOSELECTIVE SYNTHESIS OF (Z)-α,β-DISUBSTITUTED ACRYLATES

Shimagaki, Masayuki,Shiokawa, Manabu,Sugai, Kazunori,Teranaka, Tomoko,Nakata, Tadashi,Oishi, Takeshi

, p. 659 - 662 (1988)

A new route for (Z)-α,β-disubstituted acrylate is described which is made up of 1) stereoselective reduction of ketones 3 and 2) conversion of the resulting syn-2 into (Z)-1.

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