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2-Propenoic acid, 2-hydroxy-3-(4-nitrophenyl)-, methyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

103264-26-2

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103264-26-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 103264-26-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,3,2,6 and 4 respectively; the second part has 2 digits, 2 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 103264-26:
(8*1)+(7*0)+(6*3)+(5*2)+(4*6)+(3*4)+(2*2)+(1*6)=82
82 % 10 = 2
So 103264-26-2 is a valid CAS Registry Number.

103264-26-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name methyl 2-hydroxy-3-(4-nitrophenyl)-2-propenoate

1.2 Other means of identification

Product number -
Other names 4-Nitro-phenylbrenztraubensaeuremethylester

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:103264-26-2 SDS

103264-26-2Relevant academic research and scientific papers

Multi-gram synthesis of precursors of bibrachial diaza- paracyclophanes. Complexes with Zn2+, Cu2+ and Co2+ ions

Avendano, Carmen,De La Cuesta, Elena,Huck, Lena,Ortin, Irene,Gonzalez, J. Francisco

scheme or table, p. 200 - 211 (2011/05/02)

A multi-step synthetic strategy to obtain N-4-mtrophenyl-pymvoyl-amino esters at a multi-gram scale has been developed. The subsequent domino reaction promoted by catalytic hydrogenation of the nitro group gave diaza-paracyclophane 3, 13 and 14. Complexat

Chemocontrolled reduction of aromatic α-ketoesters by NaBH4: Selective synthesis of α-hydroxy esters or 1,2-diols

Dalla, Vincent,Cotelle, Philippe,Catteau, Jean Pierre

, p. 1577 - 1580 (2007/10/03)

α-Hydroxyesters 5a-g or diols 6a-g have been obtained in high yields by reduction of aromatic α-ketoesters 4 once or twice respectively by using NaBH4 as the reducer under suitable conditions. The use of a solvent that does not interact with the reagent allowed the double reduction to occur with only a slight excess of borohydride in very mild conditions.

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