Cas 796850-80-1,(1S,6S)-6-Formyl-6-methyl-cyclohex-3-enecarboxylic acid 2,2,2-trifluoro-ethyl ester

796850-80-1

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Basic information

Product Name: (1S,6S)-6-Formyl-6-methyl-cyclohex-3-enecarboxylic acid 2,2,2-trifluoro-ethyl ester
Synonyms: (1S,6S)-6-Formyl-6-methyl-cyclohex-3-enecarboxylic acid 2,2,2-trifluoro-ethyl ester
CAS NO:796850-80-1
Molecular Formula:
Molecular Weight: 250.218
EINECS: N/A
Product Categories: N/A
Mol File: 796850-80-1.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: (1S,6S)-6-Formyl-6-methyl-cyclohex-3-enecarboxylic acid 2,2,2-trifluoro-ethyl ester(CAS DataBase Reference)
NIST Chemistry Reference: (1S,6S)-6-Formyl-6-methyl-cyclohex-3-enecarboxylic acid 2,2,2-trifluoro-ethyl ester(796850-80-1)
EPA Substance Registry System: (1S,6S)-6-Formyl-6-methyl-cyclohex-3-enecarboxylic acid 2,2,2-trifluoro-ethyl ester(796850-80-1)

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: 796850-80-1(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 796850-80-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 7,9,6,8,5 and 0 respectively; the second part has 2 digits, 8 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 796850-80:
(8*7)+(7*9)+(6*6)+(5*8)+(4*5)+(3*0)+(2*8)+(1*0)=231
231 % 10 = 1
So 796850-80-1 is a valid CAS Registry Number.

796850-80-1Upstream product

796850-80-1Downstream Products

796850-92-5 1-((1S,6S)-6-Hydroxymethyl-1-methyl-cyclohex-3-enyl)-ethanol

796850-80-1Relevant articles and documents

Application of chiral cationic catalysts to several classical syntheses of racemic natural products transforms them into highly enantioselective pathways

Hu, Qi-Ying,Zhou, Gang,Corey

, p. 13708 - 13713 (2004)

This paper describes the application of chiral oxazaborolidinium cations of type 2 to various enantioselective Diels-Alder reactions that have served as early key steps for the syntheses of complex natural products. In the original syntheses these Diels-A

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