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208264-60-2

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208264-60-2 Usage

General Description

2,5-Dibromo-thiazole-4-carboxylic acid ethyl ester is a chemical compound with the molecular formula C7H6Br2NOS. It is a derivative of thiazole, a heterocyclic compound containing a five-membered ring with sulfur and nitrogen atoms. The presence of bromine atoms in the molecular structure gives the compound its distinctive properties. 2,5-Dibromo-thiazole-4-carboxylic acid ethyl ester is commonly used as an intermediate in the synthesis of pharmaceuticals and agrochemicals, and it is also utilized as a reagent in organic chemistry reactions. The compound is a colorless to pale yellow liquid at room temperature and is known for its strong odor. Proper handling and storage of 2,5-Dibromo-thiazole-4-carboxylic acid ethyl ester are important due to its potential hazards, including flammability and toxicity.

Check Digit Verification of cas no

The CAS Registry Mumber 208264-60-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,0,8,2,6 and 4 respectively; the second part has 2 digits, 6 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 208264-60:
(8*2)+(7*0)+(6*8)+(5*2)+(4*6)+(3*4)+(2*6)+(1*0)=122
122 % 10 = 2
So 208264-60-2 is a valid CAS Registry Number.
InChI:InChI=1/C6H5Br2NO2S/c1-2-11-5(10)3-4(7)12-6(8)9-3/h2H2,1H3

208264-60-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name ethyl 2,5-dibromo-1,3-thiazole-4-carboxylate

1.2 Other means of identification

Product number -
Other names 2,5-DIBROMO-THIAZOLE-4-CARBOXYLIC ACID ETHYL 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:208264-60-2 SDS

208264-60-2Relevant articles and documents

Synthesis of 2,5-dihalothiazole-4-carboxylates

Okonya, John F,Al-Obeidi, Fahad

, p. 7051 - 7053 (2007/10/03)

An efficient synthesis of 2,5-dihalothiazole-4-carboxylates has been described. Halogenation of aminothiazole carboxylate with NBS or NCS and subsequent diazotization with isoamyl nitrite and halogenation with CuBr2, CuCl2 or CH2I2 provided the corresponding diahalothiazole derivatives. The four-step process described is amenable to scale-up and requires no chromatographic purification in all the steps.

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