Cas 1146352-92-2,[(1R,2S,5R)-5-methyl-2-(1-methyl-1-phenylethyl)cyclohexyl] (2R)-2-nitromethyl-7-oxocycloheptanecarboxylate

1146352-92-2

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Basic information

Product Name: [(1R,2S,5R)-5-methyl-2-(1-methyl-1-phenylethyl)cyclohexyl] (2R)-2-nitromethyl-7-oxocycloheptanecarboxylate
Synonyms: [(1R,2S,5R)-5-methyl-2-(1-methyl-1-phenylethyl)cyclohexyl] (2R)-2-nitromethyl-7-oxocycloheptanecarboxylate
CAS NO:1146352-92-2
Molecular Formula:
Molecular Weight: 429.557
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: [(1R,2S,5R)-5-methyl-2-(1-methyl-1-phenylethyl)cyclohexyl] (2R)-2-nitromethyl-7-oxocycloheptanecarboxylate(CAS DataBase Reference)
NIST Chemistry Reference: [(1R,2S,5R)-5-methyl-2-(1-methyl-1-phenylethyl)cyclohexyl] (2R)-2-nitromethyl-7-oxocycloheptanecarboxylate(1146352-92-2)
EPA Substance Registry System: [(1R,2S,5R)-5-methyl-2-(1-methyl-1-phenylethyl)cyclohexyl] (2R)-2-nitromethyl-7-oxocycloheptanecarboxylate(1146352-92-2)

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: 1146352-92-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1146352-92-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,1,4,6,3,5 and 2 respectively; the second part has 2 digits, 9 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 1146352-92:
(9*1)+(8*1)+(7*4)+(6*6)+(5*3)+(4*5)+(3*2)+(2*9)+(1*2)=142
142 % 10 = 2
So 1146352-92-2 is a valid CAS Registry Number.

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1146352-92-2Relevant academic research and scientific papers

Synthetic studies on daphnicyclidin A: enantiocontrolled construction of the BCD ring system

Ikeda, Shuhei,Shibuya, Masatoshi,Kanoh, Naoki,Iwabuchi, Yoshiharu

, p. 1833 - 1836 (2009)

An enantiocontrolled entry to the tricyclic core of daphnicyclidin A with five chlral centers Including an all-carbon quaternary center Is reported. The synthesis features a highly dlastereoselectlve conjugate addition of nltromethane, an Ireland- Clalsen rearrangement, and a tandem acyliminium/ Mannich- type reaction.

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