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132089-44-2

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132089-44-2 Usage

General Description

2-(3-Methoxy-phenyl)-oxazole-4-carboxylic acid ethyl ester is a chemical compound with the molecular formula C14H13NO4. It belongs to the class of oxazole compounds and is used in organic synthesis and pharmaceutical research. 2-(3-METHOXY-PHENYL)-OXAZOLE-4-CARBOXYLIC ACID ETHYL ESTER is an ethyl ester derivative of 2-(3-Methoxy-phenyl)-oxazole-4-carboxylic acid, and it is often used as a building block for the synthesis of various pharmaceutical and bioactive compounds. It is a white to off-white powder with a molecular weight of 259.259 g/mol and has the potential to exhibit various biological activities, making it a valuable tool in medicinal chemistry research.

Check Digit Verification of cas no

The CAS Registry Mumber 132089-44-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,2,0,8 and 9 respectively; the second part has 2 digits, 4 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 132089-44:
(8*1)+(7*3)+(6*2)+(5*0)+(4*8)+(3*9)+(2*4)+(1*4)=112
112 % 10 = 2
So 132089-44-2 is a valid CAS Registry Number.

132089-44-2SDS

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 ethyl 2-(3-methoxyphenyl)-1,3-oxazole-4-carboxylate

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:132089-44-2 SDS

132089-44-2Relevant articles and documents

Design, synthesis and biological evaluation of 2,4-disubstituted oxazole derivatives as potential PDE4 inhibitors

Li, Ya-Sheng,Hu, De-Kun,Zhao, Dong-Sheng,Liu, Xing-Yu,Jin, Hong-Wei,Song, Gao-Peng,Cui, Zi-Ning,Zhang, Lian-Hui

, p. 1852 - 1859 (2017/03/08)

In this study, a series of pyrazole derivatives containing 4-phenyl-2-oxazole moiety were designed and synthesized in a concise way, some of which exhibited considerable inhibitory activity against PDE4B and blockade of LPS-induced TNF-α release. Compound

Palladium-catalyzed direct arylations, alkenylations, and benzylations through C-H bond cleavages with sulfamates or phosphates as electrophiles

Ackermann, Lutz,Barfuesser, Sebastian,Pospech, Jola

supporting information; experimental part, p. 724 - 726 (2010/04/02)

(Figure Presented) catalytic system comprised of Pd(OAc)2 and bldentate ligand dppe enabled first direct arylatlons with moisture-stable aryl sulfamates as electrophlles, and proved applicable to unprecedented C-H bond functlonallzations with e

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