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6303-66-8

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6303-66-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 6303-66-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,3,0 and 3 respectively; the second part has 2 digits, 6 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 6303-66:
(6*6)+(5*3)+(4*0)+(3*3)+(2*6)+(1*6)=78
78 % 10 = 8
So 6303-66-8 is a valid CAS Registry Number.
InChI:InChI=1/C10H14O4/c11-9(12)7-5-1-2-6(4-3-5)8(7)10(13)14/h5-8H,1-4H2,(H,11,12)(H,13,14)

6303-66-8SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name bicyclo[2.2.2]octane-2,3-dicarboxylic acid

1.2 Other means of identification

Product number -
Other names trans-2,3-Dicarboxybicyclo<2.2.2>octan

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:6303-66-8 SDS

6303-66-8Downstream Products

6303-66-8Relevant articles and documents

Enzymatic optical resolution of norbornanecarboxylic esters using Pig Liver Esterase

Gastel, F. J. C. van,Klunder, A. J. H.,Zwanenburg, B.

, p. 175 - 184 (2007/10/02)

The hydrolysis of a series of norbornane-type carboxylic esters catalyzed by pig liver esterase (PLE) has been investigated.It was found that an exo-ester function (syn to the C7 methylene group) is hydrolyzed with high preference.Enantioselective hydrolysis can be accomplished when a vicinal carbonyl-containing function (ester, formyl, acetyl) is present in a trans position with respect to the exo ester.The regiospecifity of the enzymatic hydrolysis has been used for the separation of exo/endo mixtures of the cycloadducts derived from cyclopentadiene and alkene esters.The regiospecifity and enantioselectivity of the enzymatic hydrolysis of norbornane-type esters were analyzed in terms of Tamm's substrate model and also by Griengl's method.

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