Cas 1170682-08-2,(1S,2R,3R,6R)-methyl 2-(4-bromophenyl)-1-cyano-3-formyl-6-hydroxycyclohexanecarboxylate

1170682-08-2

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Basic information

Product Name: (1S,2R,3R,6R)-methyl 2-(4-bromophenyl)-1-cyano-3-formyl-6-hydroxycyclohexanecarboxylate
Synonyms: (1S,2R,3R,6R)-methyl 2-(4-bromophenyl)-1-cyano-3-formyl-6-hydroxycyclohexanecarboxylate
CAS NO:1170682-08-2
Molecular Formula:
Molecular Weight: 366.211
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: (1S,2R,3R,6R)-methyl 2-(4-bromophenyl)-1-cyano-3-formyl-6-hydroxycyclohexanecarboxylate(CAS DataBase Reference)
NIST Chemistry Reference: (1S,2R,3R,6R)-methyl 2-(4-bromophenyl)-1-cyano-3-formyl-6-hydroxycyclohexanecarboxylate(1170682-08-2)
EPA Substance Registry System: (1S,2R,3R,6R)-methyl 2-(4-bromophenyl)-1-cyano-3-formyl-6-hydroxycyclohexanecarboxylate(1170682-08-2)

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: 1170682-08-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1170682-08-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,1,7,0,6,8 and 2 respectively; the second part has 2 digits, 0 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 1170682-08:
(9*1)+(8*1)+(7*7)+(6*0)+(5*6)+(4*8)+(3*2)+(2*0)+(1*8)=142
142 % 10 = 2
So 1170682-08-2 is a valid CAS Registry Number.

1170682-08-2Upstream product

1170682-08-2Downstream Products

1170682-16-2 (1R,2R,3S,4R)-2-(4-bromophenyl)-3-cyano-4-hydroxy-3-(methoxycarbonyl)cyclohexanecarboxylic acid

1170682-08-2Relevant academic research and scientific papers

Organocatalytic enantioselective domino synthesis of highly functionalized cyclohexanes with an all-carbon quaternary stereocenter

Zhao, Gui-Ling,Dziedzic, Pawel,Ullah, Farman,Eriksson, Lars,Córdova, Armando

, p. 3458 - 3462 (2009)

A highly enantioselective organocatalytic domino Michael/aldol reaction is presented. The reaction is catalyzed by chiral amines and gives access to highly functionalized cyclohexanes with one all-carbon quaternary stereocenter and multiple chiral stereoc

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