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32093-88-2

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32093-88-2 Usage

Type of Compound

Thiourea derivative

Structure

Contains a methyl group and an oxazolyl group attached to the nitrogen atom

Primary Use

Corrosion inhibitor in industrial applications

Protective Mechanism

Forms a protective film on metal surfaces

Effectiveness

Strong inhibitory properties against metal corrosion

Additional Uses

Production of pharmaceuticals, agricultural chemicals, and potential anti-cancer and anti-inflammatory properties

Application Fields

Industrial, pharmaceutical, and agricultural industries

Check Digit Verification of cas no

The CAS Registry Mumber 32093-88-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,2,0,9 and 3 respectively; the second part has 2 digits, 8 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 32093-88:
(7*3)+(6*2)+(5*0)+(4*9)+(3*3)+(2*8)+(1*8)=102
102 % 10 = 2
So 32093-88-2 is a valid CAS Registry Number.

32093-88-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-methyl-3-(1,3-oxazol-2-yl)thiourea

1.2 Other means of identification

Product number -
Other names 1-methyl-3-oxazol-2-yl-thiourea

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:32093-88-2 SDS

32093-88-2Downstream Products

32093-88-2Relevant articles and documents

Formation of Thioamide Derivatives from Reactions of Isothiocyanates with Oxazol-2-amines

Crank, George,Khan, Humaid R.

, p. 447 - 458 (2007/10/02)

4-Substituted oxazol-2-amines react with isothiocyanates to give products having a thioamide function at C5.The reaction is considered to be an electrophilic process in competition with the usual reaction of the amino group with the isothiocyanate.The nature of the isothiocyanate and the type of substituent at C4 affect the amount of the thioamide product formed.Some chemical properties of the thioamides are also investigated.

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