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78941-77-2

78941-77-2

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78941-77-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 78941-77-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,8,9,4 and 1 respectively; the second part has 2 digits, 7 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 78941-77:
(7*7)+(6*8)+(5*9)+(4*4)+(3*1)+(2*7)+(1*7)=182
182 % 10 = 2
So 78941-77-2 is a valid CAS Registry Number.
InChI:InChI=1/C15H13NO3/c17-12(16-7-4-2-1-3-5-7)14-8-6-9-11(10(8)14)15(9,14)13(18)19/h1-5,8-11H,6H2,(H,16,17)(H,18,19)

78941-77-2SDS

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 5-((PHENYLAMINO(CARBONYL)TETRACYCLO(3.2.0.02,7.04,6)HEPTANE-2-CARBOXYL IC ACID

1.2 Other means of identification

Product number -
Other names -

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:78941-77-2 SDS

78941-77-2Relevant articles and documents

Valence Isomerization between Water-soluble Norbornadiene and Quadricyclane Derivative

Maruyama, Kazuhiro,Tamiaki, Hitoshi,Yanai, Tetsuya

, p. 781 - 782 (2007/10/02)

Photoisomerization of 3-(arylcarbamoyl)-norbornadiene-2-carboxylic acid 1 to the corresponding quadricyclane derivative 2 in an aqueous alkaline solution was clean and dependent upon the p-substituent of the aryl group.The exothermically reversal reaction

A WATER-SOLUBLE SOLAR ENERGY STORAGE SYSTEM

Maruyama, Kazuhiro,Tamiaki, Hitoshi

, p. 1699 - 1702 (2007/10/02)

In an alkaline aqueous solution, photochemical valence isomerization of norbornadiene derivative 1 to quadricyclane derivative 2 occurred quantitatively, and reverse isomerization of 2 to 1 under release of heat was achived by catalytic action of cobalt h

HIGHLY EFFICIENT VALENCE ISOMERIZATION BETWEEN NORBORNADIENE AND QUADRICYCLANE DERIVATIVES UNDER SUNLIGHT

Maruyama, Kazuhiro,Terada, Kazutoshi,Yamamoto, Yoshinori

, p. 839 - 842 (2007/10/02)

3-Phenylcarbamoyl-2,5-norbornadiene-2-carboxylic acid (1b) undergoes a facile and quantitative isomerization into the corresponding quadricyclane derivative (2b) under sunlight.The back isomerization of 2b to 1b proceeds quantitatively by the use of catal

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