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23994-89-0

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23994-89-0 Usage

Also known as

Ethyl 2-sulfanyl-4,5-dihydro-1,3-thiazole-5-carboxylate

Type of compound

Sulfur-containing heterocyclic compound

Usage

Intermediate in the synthesis of pharmaceuticals and agrochemicals

Structure

Thiazole ring with an ethylsulfanyl group

Value in organic synthesis

Valuable building block

Known properties

Antimicrobial, antifungal, and anti-inflammatory

Importance in pharmaceutical industry

Target for further research and development

Check Digit Verification of cas no

The CAS Registry Mumber 23994-89-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,3,9,9 and 4 respectively; the second part has 2 digits, 8 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 23994-89:
(7*2)+(6*3)+(5*9)+(4*9)+(3*4)+(2*8)+(1*9)=150
150 % 10 = 0
So 23994-89-0 is a valid CAS Registry Number.

23994-89-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-ethylsulfanyl-4,5-dihydro-1,3-thiazole

1.2 Other means of identification

Product number -
Other names 2-ethylsulfanyl-4,5-dihydro-thiazole

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:23994-89-0 SDS

23994-89-0Relevant articles and documents

A more than the penem matching bends down the ester side chain new synthetic method

-

Paragraph 0046-0047, (2017/08/25)

The invention discloses a novel synthetic method of a tebipenem pivoxil side chain. The method employs cheap and easily available raw material, has simple experimental operations, high overall yield and is applicable to industrialized production.

Studies of 2 substituted thiazolines. I. Reaction with cyanoacetic acid

Sakurai,Kurumi,Okutome,et al.

, p. 1426 - 1430 (2007/10/04)

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