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57314-13-3

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57314-13-3 Usage

General Description

2,4,5-Tribromothiazole is an organobromine compound used as an intermediate in the synthesis of pharmaceuticals and agricultural chemicals. It is a highly reactive substance with a distinct odor and high toxicity. 2,4,5-Tribromothiazole is classified as a POSSIBLE human carcinogen and is known to cause skin and eye irritation upon direct contact. Due to its potential health hazards, proper handling and safety precautions are necessary when working with this chemical. Its application and use are regulated and restricted in many countries to minimize exposure and potential harm to humans and the environment.

Check Digit Verification of cas no

The CAS Registry Mumber 57314-13-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,7,3,1 and 4 respectively; the second part has 2 digits, 1 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 57314-13:
(7*5)+(6*7)+(5*3)+(4*1)+(3*4)+(2*1)+(1*3)=113
113 % 10 = 3
So 57314-13-3 is a valid CAS Registry Number.

57314-13-3SDS

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 2,4,5-Tribromo-1,3-thiazole

1.2 Other means of identification

Product number -
Other names Thiazole,tribromo

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:57314-13-3 SDS

57314-13-3Upstream product

57314-13-3Relevant articles and documents

Synthesis of Brominated Thiazoles via Sequential Bromination-Debromination Methods

Uzelac, Eric J.,Rasmussen, Seth C.

, p. 5947 - 5951 (2017/06/07)

The synthesis of the full family of bromothiazoles has been revisited in order to update and optimize their production. The species reported include 2-bromothiazole, 4-bromothiazole, 5-bromothiazole, 2,4-dibromothiazole, 2,5-dibromothiazole, 4,5-dibromothiazole, and 2,4,5-tribromothiazole, the majority of which are produced via sequential bromination and debromination steps. This complete family can now be produced without the use of elemental bromine, and the presented methods have allowed the physical and NMR spectroscopic characterization of the full family to be reported for the first time.

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