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89205-08-3

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89205-08-3 Usage

General Description

5-(2,4-DIMETHYOXYPHENYL)-1,3-OXAZOLE-4-CARBOXYLIC ACID is a chemical compound that belongs to the oxazole carboxylic acid class. It is a derivative of 1,3-oxazole-4-carboxylic acid and contains a dimethoxyphenyl group. 5-(2,4-DIMETHYOXYPHENYL)-1,3-OXAZOLE-4-CARBOXYLIC ACID is used in pharmaceutical research and drug development due to its potential pharmacological properties. It may have applications in the treatment of various diseases and conditions, although further research is needed to fully understand its potential medicinal uses. Additionally, it may also have industrial applications in the synthesis of other organic compounds.

Check Digit Verification of cas no

The CAS Registry Mumber 89205-08-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,9,2,0 and 5 respectively; the second part has 2 digits, 0 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 89205-08:
(7*8)+(6*9)+(5*2)+(4*0)+(3*5)+(2*0)+(1*8)=143
143 % 10 = 3
So 89205-08-3 is a valid CAS Registry Number.

89205-08-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 5-(3,4-Dimethoxyphenyl)-1,3-oxazole-4-carboxylic acid

1.2 Other means of identification

Product number -
Other names 4-Oxazolecarboxylicacid,5-(3,4-dimethoxyphenyl)

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:89205-08-3 SDS

89205-08-3Downstream Products

89205-08-3Relevant articles and documents

Syntheses of 5-substituted oxazole-4-carboxylic acid derivatives with inhibitory activity on blood platelet aggregation

Ozaki,Maeda,Iwasaki,Matsumoto,Odawara,Sasaki,Morita

, p. 4417 - 4424 (2007/10/02)

Methyl 5-substituted oxazole-4-carboxylates were synthesized by the reaction of methyl α-isocyanoacetate with acylating reagents in the presence of bases. The oxazole methyl esters were converted into the carboxylic acids and the carboxamides. Then, N-alk

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