Cas 1515876-18-2,ethyl (1R,2S,3S,4R,5S,6S)-2-hydroxy-2-methyl-5-nitro-4-phenyl-3-formyl-6-(4-chlorophenyl)cyclohexanecarboxylate

1515876-18-2

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Basic information

Product Name: ethyl (1R,2S,3S,4R,5S,6S)-2-hydroxy-2-methyl-5-nitro-4-phenyl-3-formyl-6-(4-chlorophenyl)cyclohexanecarboxylate
Synonyms:
CAS NO:1515876-18-2
Molecular Formula:
Molecular Weight: 445.9
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: ethyl (1R,2S,3S,4R,5S,6S)-2-hydroxy-2-methyl-5-nitro-4-phenyl-3-formyl-6-(4-chlorophenyl)cyclohexanecarboxylate(CAS DataBase Reference)
NIST Chemistry Reference: ethyl (1R,2S,3S,4R,5S,6S)-2-hydroxy-2-methyl-5-nitro-4-phenyl-3-formyl-6-(4-chlorophenyl)cyclohexanecarboxylate(1515876-18-2)
EPA Substance Registry System: ethyl (1R,2S,3S,4R,5S,6S)-2-hydroxy-2-methyl-5-nitro-4-phenyl-3-formyl-6-(4-chlorophenyl)cyclohexanecarboxylate(1515876-18-2)

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: 1515876-18-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1515876-18-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,5,1,5,8,7 and 6 respectively; the second part has 2 digits, 1 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 1515876-18:
(9*1)+(8*5)+(7*1)+(6*5)+(5*8)+(4*7)+(3*6)+(2*1)+(1*8)=182
182 % 10 = 2
So 1515876-18-2 is a valid CAS Registry Number.

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1515876-18-2Relevant academic research and scientific papers

Synthesis of nonracemic polysubstituted cyclohexanes through cascade reactions of (2R,3S)-2-Acetyl-3-aryl-4-nitrobutanoates, Adducts of Ni(II)-catalyzed michael addition

Reznikov,Sidnin,Klimochkin

, p. 1600 - 1604 (2014/02/14)

Stereoselective synthesis of ethyl-4,6-diaryl-2-hydroxy-2-methyl-5-nitro-3- formylcyclohexanecarboxylates was described. The formation of the asymmetric site of the required configuration is achieved by an enantioselective Michael addition of ethyl acetoa

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