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Butanedioic acid, (1-cyclohexen-1-ylmethyl)hydroxyoxo-, dimethyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

130954-07-3

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130954-07-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 130954-07-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,0,9,5 and 4 respectively; the second part has 2 digits, 0 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 130954-07:
(8*1)+(7*3)+(6*0)+(5*9)+(4*5)+(3*4)+(2*0)+(1*7)=113
113 % 10 = 3
So 130954-07-3 is a valid CAS Registry Number.

130954-07-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name dimethyl 2-(cyclohexen-1-ylmethyl)-2-hydroxy-3-oxobutanedioate

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:130954-07-3 SDS

130954-07-3Relevant academic research and scientific papers

Investigation of the mechanisms of ene reactions of carbonyl enophiles by intermolecular and intramolecular hydrogen-deuterium isotope effects: Partitioning of reaction intermediates

Song, Zhiguo,Beak, Peter

, p. 8126 - 8134 (1990)

The mechanisms of ene reactions of selected carbonyl enophiles with methylenecyclohexane (1) and 1-methylenetetralin (2) have been investigated by determinations of intermolecular and intramolecular hydrogen-deuterium isotope effects. In the thermal ene r

Ene Reactions of Dialkyl Dioxosuccinate Esters

Beak, Peter,Song, Zhiguo,Resek, James E.

, p. 944 - 947 (2007/10/02)

The ene reactions of dimethyl dioxosuccinate (1) and of diethyl dioxosuccinate (2) with olefins give the expected addition products.The reactions of 1 with vinyl ethers or an eneamine provide the cyclopentenones 15 and 16 in a sequence which is consistent with an ene reaction followed by a cyclization.The tin tetrachloride catalyzed conversion of 6 to 17 provides an example of a formal type II ene reaction to give a cyclopentyl ring.However, the stereochemistry of 17 suggests the reaction involves a stepwise ionic process.

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