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3-Benzylidene-2-oxo-cyclopentanecarboxylic acid ethyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

95127-15-4

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95127-15-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 95127-15-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,5,1,2 and 7 respectively; the second part has 2 digits, 1 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 95127-15:
(7*9)+(6*5)+(5*1)+(4*2)+(3*7)+(2*1)+(1*5)=134
134 % 10 = 4
So 95127-15-4 is a valid CAS Registry Number.
InChI:InChI=1/C15H16O3/c1-2-18-15(17)13-9-8-12(14(13)16)10-11-6-4-3-5-7-11/h3-7,10,13H,2,8-9H2,1H3/b12-10+

95127-15-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-Benzylidene-2-oxo-cyclopentanecarboxylic acid ethyl ester

1.2 Other means of identification

Product number -
Other names benzylidene-(4-benzylsulfanyl-2-phenyl-oxazol-5-yl)-amine

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:95127-15-4 SDS

95127-15-4Relevant academic research and scientific papers

Investigation of the mechanism for the preparation of 6-phenyl-2,4- dioxotetrahydropyrans by the potassium carbonate promoted condensation between acetoacetate esters and benzaldehyde

Andersh, Brad,Nguyen, Elizabeth T.,Van Hoveln, Ryan J.,Kemmerer, Dylan K.,Baudo, David A.,Graves, Jessica A.,Roark, Mollie E.,Bosma, Wayne B.

, p. 4563 - 4567 (2013/06/05)

Treatment of benzaldehyde and an acetoacetate ester with potassium carbonate in an alcohol solvent proceeds via γ-C-alkylation rather than α-C-alkylation resulting in the formation of 6-phenyl-2,4- dioxotetrahydropyran. Based upon results from deuterium e

User-friendly stereoselective one-pot access to 1,4-diazepane derivatives by a cyclodehydrative three-component reaction with 1,3-dicarbonyls

Sotoca, Enrique,Allais, Christophe,Constantieux, Thierry,Rodriguez, Jean

experimental part, p. 1911 - 1920 (2009/06/28)

A multicomponent reaction of 1,3-dicarbonyls with 1,2-diamines and aromatic aldehydes is described for the direct stereoselective synthesis of 1,4-diazepane derivatives. Various reaction conditions were tested, including an efficient, user-friendly solven

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