Cas 476153-60-3,bicyclo[2.2.2]octa-2,5-diene-1,2,3-tricarboxylic acid 1-<i>tert</i>-butyl ester 2,3-dimethyl ester

476153-60-3

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Basic information

Product Name: bicyclo[2.2.2]octa-2,5-diene-1,2,3-tricarboxylic acid 1-tert-butyl ester 2,3-dimethyl ester
Synonyms:
CAS NO:476153-60-3
Molecular Formula:
Molecular Weight: 322.358
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: bicyclo[2.2.2]octa-2,5-diene-1,2,3-tricarboxylic acid 1-tert-butyl ester 2,3-dimethyl ester(CAS DataBase Reference)
NIST Chemistry Reference: bicyclo[2.2.2]octa-2,5-diene-1,2,3-tricarboxylic acid 1-tert-butyl ester 2,3-dimethyl ester(476153-60-3)
EPA Substance Registry System: bicyclo[2.2.2]octa-2,5-diene-1,2,3-tricarboxylic acid 1-tert-butyl ester 2,3-dimethyl ester(476153-60-3)

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: 476153-60-3(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 476153-60-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 4,7,6,1,5 and 3 respectively; the second part has 2 digits, 6 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 476153-60:
(8*4)+(7*7)+(6*6)+(5*1)+(4*5)+(3*3)+(2*6)+(1*0)=163
163 % 10 = 3
So 476153-60-3 is a valid CAS Registry Number.

476153-60-3Upstream product

762-42-5 dimethyl acetylenedicarboxylate

476153-60-3Downstream Products

476153-60-3Relevant academic research and scientific papers

Regiospecific synthesis of a bridgehead-functionalized bicyclo[2.2.2]octenone

Kende, Andrew S.,Lan, Jiong,Arad, Dorit

, p. 5237 - 5239 (2002)

Three independent strategies are tested toward the synthesis of the protected 1-aminobicyclo[2.2.2]octene ketodiester 1. One of these three is found to be completely regioselective. It proceeds by Diels-Alder addition of dimethyl acetylenedicarboxylate to

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