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Bicyclo[2.2.1]hepta-2,5-diene-2,3-dicarboxylic acid dimethyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

947-57-9

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947-57-9 Usage

Synthesis Reference(s)

The Journal of Organic Chemistry, 48, p. 1096, 1983 DOI: 10.1021/jo00155a033

Check Digit Verification of cas no

The CAS Registry Mumber 947-57-9 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 9,4 and 7 respectively; the second part has 2 digits, 5 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 947-57:
(5*9)+(4*4)+(3*7)+(2*5)+(1*7)=99
99 % 10 = 9
So 947-57-9 is a valid CAS Registry Number.
InChI:InChI=1/C11H12O4/c1-14-10(12)8-6-3-4-7(5-6)9(8)11(13)15-2/h3-4,6-7H,5H2,1-2H3

947-57-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name dimethyl bicyclo[2.2.1]hepta-2,5-diene-2,3-dicarboxylate

1.2 Other means of identification

Product number -
Other names 2,3-dicarbomethoxynorbornadiene

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:947-57-9 SDS

947-57-9Relevant academic research and scientific papers

Enehydrazines, 34. The Addition of Methylhydrazine to Dimethyl Acetylenedicarboxylate is Reversible

Sucrow, Wolfgang,Bredthauer, Gerhard

, p. 1520 - 1524 (2007/10/02)

The cyclisation of the enehydrazine 1 to the pyrazolone 5 proceeds by cleavage of 1 to its educts 2 and 3 followed by their recombination to 4.Addition of 2 or 3 supresses the dissociation of 1, furthermore 2 and 3 could be separately captured from 1.

Structure-Reactivity Factors for Exciplex Isomerization of Quadricyclene and Related Compounds

Jones, Guilford,Chiang, Sheau-Hwa,Becker, William G.,Greenberg, Don P.

, p. 681 - 683 (2007/10/02)

The quadricyclenes (1) and (3) are equally effective in exciplex isomerization although other cage hydrocarbons do not undergo efficient reaction when sensitized by aromatic fluorophores; irradiation of charge-transfer complexes of (1) and (3) and electron-deficient alkenes results in efficient valence but not geometrical isomerization.

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