Cas 127896-75-7,(5E,11E)-Dibenzo[a,e]cyclooctene-5,11-dicarboxylic acid 5-((1R,2S,5R)-2-isopropyl-5-methyl-cyclohexyl) ester 11-methyl ester

127896-75-7

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Basic information

Product Name: (5E,11E)-Dibenzo[a,e]cyclooctene-5,11-dicarboxylic acid 5-((1R,2S,5R)-2-isopropyl-5-methyl-cyclohexyl) ester 11-methyl ester
Synonyms:
CAS NO:127896-75-7
Molecular Formula:
Molecular Weight: 444.571
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: (5E,11E)-Dibenzo[a,e]cyclooctene-5,11-dicarboxylic acid 5-((1R,2S,5R)-2-isopropyl-5-methyl-cyclohexyl) ester 11-methyl ester(CAS DataBase Reference)
NIST Chemistry Reference: (5E,11E)-Dibenzo[a,e]cyclooctene-5,11-dicarboxylic acid 5-((1R,2S,5R)-2-isopropyl-5-methyl-cyclohexyl) ester 11-methyl ester(127896-75-7)
EPA Substance Registry System: (5E,11E)-Dibenzo[a,e]cyclooctene-5,11-dicarboxylic acid 5-((1R,2S,5R)-2-isopropyl-5-methyl-cyclohexyl) ester 11-methyl ester(127896-75-7)

Safety Data

Hazard Codes: N/A
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Safety Statements: N/A
WGK Germany:
RTECS:
HazardClass: N/A
PackingGroup: N/A
Hazardous Substances Data: 127896-75-7(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 127896-75-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,7,8,9 and 6 respectively; the second part has 2 digits, 7 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 127896-75:
(8*1)+(7*2)+(6*7)+(5*8)+(4*9)+(3*6)+(2*7)+(1*5)=177
177 % 10 = 7
So 127896-75-7 is a valid CAS Registry Number.

127896-75-7Upstream product

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127896-75-7Relevant academic research and scientific papers

CHIRAL HANDLE-INDUCED DIASTEREOSELECTIVITY IN AN ORGANIC PHOTOREARRANGEMENT: SOLUTION VERSUS SOLID STATE RESULTS

Chen, Jianxin,Garcia-Garibay, Miguel,Scheffer, John R.

, p. 6125 - 6128 (1989)

The degree of asymmetric induction in the di-?-methane photorearrangement due to the presence of a remote chiral handle was found to vary with the nature and location of the chiral handle and with the medium in which the reaction was carried out.

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