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Bicyclo[2.2.1]hepta-2,5-diene-2-carboxylic acid, 3-[(phenylamino)carbonyl]- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

78941-78-3

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78941-78-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 78941-78-3 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 8 respectively.
Calculate Digit Verification of CAS Registry Number 78941-78:
(7*7)+(6*8)+(5*9)+(4*4)+(3*1)+(2*7)+(1*8)=183
183 % 10 = 3
So 78941-78-3 is a valid CAS Registry Number.

78941-78-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-phenylcarbamoyl-2,5-norbornadiene-2-carboxylic acid

1.2 Other means of identification

Product number -
Other names 3-(phenylcarbamoyl)norbornadiene-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:78941-78-3 SDS

78941-78-3Relevant academic research and scientific papers

INSOLUBLE CATALYST FOR HEAT-GAIN IN A WATER-SOLUBLE SOLAR ENERGY STORAGE SYSTEM

Maruyama, Kazuhiro,Tamiaki, Hitoshi,Kawabata, Shigeki

, p. 743 - 746 (1984)

By action of insoluble catalysts, cobalt tetraphenylporphyrin or cobalt phthalocyanine adsorbed on activated carbon, water-soluble quadricyclane derivative was isomerized to norbornadiene derivative under release of heat in an alkaline solution.The activi

Exothermic Isomerization of Water-soluble Quadricyclanes to Norbornadienes by Soluble and Insoluble Catalysts

Maruyama, Kazuhiro,Tamiaki, Hitoshi,Kawabata, Shigeki

, p. 543 - 550 (2007/10/02)

Water-soluble quadricyclane derivatives (1) were stable in an aqueous sodium carbonate solution, but addition of a catalytic amount of water-soluble cobalt porphyrin complexes (3) induced rapid and quantitative isomerization of (1) to norbornadiene derivatives (2) under release of heat.Insoluble catalysts (4) prepared by adsorption of Co-TPP or Co-Pc on activated carbon were similarly active as the soluble analogues.They were stable enough to keep high activities for recycling use.

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

Exploitation of Solar Energy Storage Systems. Valence Isomerization between Norbornadiene and Quadricyclane Derivatives

Maruyama, Kazuhiro,Terada, Kazutoshi,Yamamoto, Yoshinori

, p. 5294 - 5300 (2007/10/02)

Use of copper(I)-nitrogen ligand catalysts such as Ph3PCuCl*bpy (3), Ph3PCuCl*phen (4), Ph3PCuCl*phtha (5), and Ph3PCuBr*py (6) enables the photochemical isomerization of norbornadiene to quadricyclane to be performed at a longer wavelength than 350 nm, a

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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