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CAS

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6343-10-8

Bicyclo[2.2.1]heptane-2,3-dicarboxamide is a cyclic organic compound with the molecular formula C9H13NO2. It features a bicyclic structure with two carbonyl groups (amide groups) attached to the second and third carbon atoms of the seven-membered ring. bicyclo[2.2.1]heptane-2,3-dicarboxamide is known for its potential applications in the synthesis of various pharmaceuticals and agrochemicals due to its unique structural properties. It can be synthesized through various methods, including the reaction of bicyclo[2.2.1]heptane-2,3-dicarboxylic acid with amines. The compound's stability and reactivity make it a valuable intermediate in organic chemistry, particularly in the development of complex molecular architectures.

6343-10-8

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6343-10-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 6343-10-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,3,4 and 3 respectively; the second part has 2 digits, 1 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 6343-10:
(6*6)+(5*3)+(4*4)+(3*3)+(2*1)+(1*0)=78
78 % 10 = 8
So 6343-10-8 is a valid CAS Registry Number.

6343-10-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name bicyclo[2.2.1]heptane-2,3-dicarboxamide

1.2 Other means of identification

Product number -
Other names HMS3088P18

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:6343-10-8 SDS

6343-10-8Upstream product

6343-10-8Downstream Products

6343-10-8Relevant articles and documents

Cationic Chiral Fluorinated Oxazaborolidines. More Potent, Second-Generation Catalysts for Highly Enantioselective Cycloaddition Reactions

Mahender Reddy, Karla,Bhimireddy, Eswar,Thirupathi, Barla,Breitler, Simon,Yu, Shunming,Corey

, p. 2443 - 2453 (2016)

The coordination of chiral ligands to Lewis acid metal derivatives, a useful strategy for enantioselective, electrophilic catalysis, generally leads to a lower level of catalytic activity than that of the original uncomplexed compound. Activation by furth

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