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148122-20-7

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148122-20-7 Usage

Type of compound

Ester derivative of oxadiazole-3-carboxylic acid

Primary use

Building block for the synthesis of various drugs and bioactive compounds in the pharmaceutical industry

Known biological activities

Anti-inflammatory and antimicrobial properties

Physical state

White crystalline solid

Melting point

Around 134-137°C

Solubility

Soluble in organic solvents such as dimethyl sulfoxide and ethyl acetate

Interest in research

Medicinal chemistry and drug discovery due to its versatile nature and potential therapeutic applications

Check Digit Verification of cas no

The CAS Registry Mumber 148122-20-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,8,1,2 and 2 respectively; the second part has 2 digits, 2 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 148122-20:
(8*1)+(7*4)+(6*8)+(5*1)+(4*2)+(3*2)+(2*2)+(1*0)=107
107 % 10 = 7
So 148122-20-7 is a valid CAS Registry Number.

148122-20-7SDS

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 methyl 1,2,5-oxadiazole-3-carboxylate

1.2 Other means of identification

Product number -
Other names 1,2,5-oxadiazole-3-carboxylic acid methyl ester

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:148122-20-7 SDS

148122-20-7Downstream Products

148122-20-7Relevant articles and documents

MONOSUBSTITUTED FURAZANES. I. NMR INVESTIGATION

Strelenko, Yu. A.,Sheremetev, A. B.,Khmel'nitskii, L. I.

, p. 927 - 930 (1992)

The 1H, 13C, 15N and 17O NMR spectral parameters were obtained for monosubstituted furazanes and the 13C NMR chemical shifts of these compounds were correlated with the chemical shifts of monosubstituted benzenes.

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