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197719-27-0

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197719-27-0 Usage

General Description

2,5-Dimethyl-1,3-oxazole-4-carbonyl Chloride is a unique chemical compound primarily used in the synthesis of other complex compounds. It belongs to the group of oxazoles, which are heterocyclic compounds containing an oxygen and a nitrogen atom in a five-membered ring formation. 2,5-DIMETHYL-1,3-OXAZOLE-4-CARBONYL CHLORIDE is generally used in a variety of industries, most commonly in pharmaceuticals, due to its ability to form other molecules. Its chemical formula is C6H6ClNO2. The detailed properties or potential hazards of this specific compound are not readily available, emphasizing the importance of handling it within controlled settings by trained professionals.

Check Digit Verification of cas no

The CAS Registry Mumber 197719-27-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,9,7,7,1 and 9 respectively; the second part has 2 digits, 2 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 197719-27:
(8*1)+(7*9)+(6*7)+(5*7)+(4*1)+(3*9)+(2*2)+(1*7)=190
190 % 10 = 0
So 197719-27-0 is a valid CAS Registry Number.
InChI:InChI=1/C6H6ClNO2/c1-3-5(6(7)9)8-4(2)10-3/h1-2H3

197719-27-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name 2,5-DIMETHYL-1,3-OXAZOLE-4-CARBONYL CHLORIDE

1.2 Other means of identification

Product number -
Other names 2,5-Dimethyl-4-chlorocarbonyl-1,3-oxazole

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:197719-27-0 SDS

197719-27-0Relevant articles and documents

The synthesis of oxazoles by thermolysis or photolysis of 2-acylisoxazol-5-ones

Ang, Kiah H.,Prager, Rolf H.,Smith, Jason A.,Weber, Ben,Williams, Craig M.

, p. 675 - 678 (2007/10/02)

N-acylisoxazol-5-ones are converted into the corresponding 2-substituted oxazoles by photolysis at 300 or 254 nm, or by flash vacuum pyrolysis. The former procedure is favoured for isoxazolones with electron withdrawing groups at C-4, and pyrolysis for all others.

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