Cas 1380204-19-2,6-meta-chlorophenyl-3-formyl-2-hydroxy-2-methyl-5-nitro-4-phenylcyclohexanecarboxylic acid methyl ester

1380204-19-2

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Basic information

Product Name: 6-meta-chlorophenyl-3-formyl-2-hydroxy-2-methyl-5-nitro-4-phenylcyclohexanecarboxylic acid methyl ester
Synonyms:
CAS NO:1380204-19-2
Molecular Formula:
Molecular Weight: 431.873
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: 6-meta-chlorophenyl-3-formyl-2-hydroxy-2-methyl-5-nitro-4-phenylcyclohexanecarboxylic acid methyl ester(CAS DataBase Reference)
NIST Chemistry Reference: 6-meta-chlorophenyl-3-formyl-2-hydroxy-2-methyl-5-nitro-4-phenylcyclohexanecarboxylic acid methyl ester(1380204-19-2)
EPA Substance Registry System: 6-meta-chlorophenyl-3-formyl-2-hydroxy-2-methyl-5-nitro-4-phenylcyclohexanecarboxylic acid methyl ester(1380204-19-2)

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: 1380204-19-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1380204-19-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,8,0,2,0 and 4 respectively; the second part has 2 digits, 1 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 1380204-19:
(9*1)+(8*3)+(7*8)+(6*0)+(5*2)+(4*0)+(3*4)+(2*1)+(1*9)=122
122 % 10 = 2
So 1380204-19-2 is a valid CAS Registry Number.

1380204-19-2Upstream product

104-55-2 3-phenyl-propenal

1380204-19-2Downstream Products

1380204-19-2Relevant academic research and scientific papers

Control of six contiguous stereocenters in an asymmetric organocatalytic one-pot Michael/Michael/aldol addition sequence

Enders, Dieter,Urbanietz, Gregor,Cassens-Sasse, Elisa,Keess, Sebastian,Raabe, Gerhard

, p. 1481 - 1488 (2012)

The asymmetric organocatalytic one-pot synthesis of polyfunctionalized cyclohexanes is described. Starting from β-keto esters, nitroalkenes and α,β-unstaturated aldehydes and employing a bifunctional norephedrine-based thiourea catalyst, six contiguous st

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