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3-(naphthalen-1-ylcarbamoyl)-7-oxabicyclo[2.2.1]heptane-2-carboxylic acid is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

69727-37-3

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69727-37-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 69727-37-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,9,7,2 and 7 respectively; the second part has 2 digits, 3 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 69727-37:
(7*6)+(6*9)+(5*7)+(4*2)+(3*7)+(2*3)+(1*7)=173
173 % 10 = 3
So 69727-37-3 is a valid CAS Registry Number.

69727-37-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-(naphthalen-1-ylcarbamoyl)-7-oxabicyclo[2.2.1]heptane-3-carboxylic acid

1.2 Other means of identification

Product number -
Other names 3-(naphthalen-1-ylcarbamoyl)-7-oxabicyclo[2.2.1]heptane-2-carboxylic acid

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:69727-37-3 SDS

69727-37-3Downstream Products

69727-37-3Relevant academic research and scientific papers

Synthesis and Anticonvulsant Activity of 7-Oxabicycloheptane Derivatives: Part II - N-Alkyl, N-Aryl and N-Heteroaryl Derivatives of 3,6-Epoxyhexahydrophthalic Acid Amide

Joshi, Balawant S.,David, Joy,Gawad, Dilip H.

, p. 136 - 139 (2007/10/02)

A series of (fifty) N-substituted 3,6-epoxyhexahydrophthalic acid amides have been prepared by the reaction of exo-cis-7-oxabicycloheptane-2,3-dicarboxylic anhydride with primary amines in benzene.Many of the compounds show anticonvulsant activity against electroshock, metrazol, strychnine and picrotoxin induced convulsions.Several compounds are found to be superior to ethosuximide and sodium valproate in anti-electroshock and antimetrazol test systems.

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