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10200-43-8

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10200-43-8 Usage

Chemical Properties

White solid

Check Digit Verification of cas no

The CAS Registry Mumber 10200-43-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,0,2,0 and 0 respectively; the second part has 2 digits, 4 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 10200-43:
(7*1)+(6*0)+(5*2)+(4*0)+(3*0)+(2*4)+(1*3)=28
28 % 10 = 8
So 10200-43-8 is a valid CAS Registry Number.
InChI:InChI=1/C7H9NO3/c1-3-10-7(9)6-4-11-5(2)8-6/h4H,3H2,1-2H3

10200-43-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name ethyl 2-methyl-1,3-oxazole-4-carboxylate

1.2 Other means of identification

Product number -
Other names ethyl 2-methyloxazole-4-carboxylate

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:10200-43-8 SDS

10200-43-8Relevant articles and documents

DIRECT PREPARATION OF 4-CARBOETHOXY-1,3-OXAZOLES

Connell, Richard D.,Tebbe, Mark,Helquist, Paul,Akermark, Bjoern

, p. 17 - 20 (1991)

The diazoaldehyde ester N2C(CHO)CO2Et undergoes rhodium-catalyzed reaction with nitriles to give 4-carboethoxy-1,3-oxazoles directly.

Facile synthesis of oxazoles starting from ketones

Lee, Jong Chan,Kim, Sehyun,Lee, Yong Chan

, p. 1611 - 1614 (2003)

A new and efficient method for the preparation of 2,4- and 2,4,5-substituted oxazoles is described which is based upon the reaction of α-sulfonyloxy ketone intermediates with acetamide or benzamide.

Direct palladium-catalyzed alkenylation, benzylation and alkylation of ethyl oxazole-4-carboxylate with alkenyl-, benzyl- and alkyl halides

Verrier, Cecile,Hoarau, Christophe,Marsais, Francis

supporting information; experimental part, p. 647 - 650 (2009/06/20)

The ethyl oxazole-4-carboxylate was directly and regioselectively alkenylated, benzylated and alkylated with alkenyl-, benzyl-, allyl- and alkyl halides in the presence of catalytic amounts of palladium acetate with caesium carbonate using Buchwald's John

Atropisomers of 3-heteroaryl-4(3H)-quinazolinones for the treatment of neurodegenerative and CNS-trauma related conditions

-

, (2008/06/13)

The present invention relates to novel atropisomers of 3-heteroaryl-4(3H)-quinazolinones of the formula Ia, and their pharmaceutically acceptable salts, and pharmaceutical compositions and methods of treating neurodegenerative and CNS-trauma related conditions.

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