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2(3H)-Thiazolethione, 4-[(acetyloxy)methyl]-3-(2,3,4-trifluorophenyl)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

136708-89-9

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136708-89-9 Usage

Thiazolethione ring

The compound contains a 2(3H)-thiazolethione ring, which is a heterocyclic compound with various biological activities.

Trifluorophenyl group

The compound has a 2,3,4-trifluorophenyl group attached to the thiazolethione ring, which may impart specific properties or reactivity to the compound.

Acetyloxy methyl group

The compound contains an acetyloxymethyl group, which is a functional group consisting of an acetyl group bonded to a methoxy group.

Potential uses in pharmaceuticals or organic synthesis

The presence of the thiazolethione ring and the trifluorophenyl group make the compound potentially useful in pharmaceuticals or organic synthesis.

Further study needed

Further study and analysis of the compound may be necessary to fully understand its potential uses and properties.

Check Digit Verification of cas no

The CAS Registry Mumber 136708-89-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,6,7,0 and 8 respectively; the second part has 2 digits, 8 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 136708-89:
(8*1)+(7*3)+(6*6)+(5*7)+(4*0)+(3*8)+(2*8)+(1*9)=149
149 % 10 = 9
So 136708-89-9 is a valid CAS Registry Number.

136708-89-9SDS

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-sulfanylidene-3-(2,3,4-trifluorophenyl)-1,3-thiazol-4-yl]methyl acetate

1.2 Other means of identification

Product number -
Other names 4-(acetoxymethyl)-3-(2,3,4-trifluorophenyl)-2(3H)-thiazolethione

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:136708-89-9 SDS

136708-89-9Upstream product

136708-89-9Downstream Products

136708-89-9Relevant academic research and scientific papers

Synthesis and antibacterial activity of new tetracyclic quinolone antibacterials

Taguchi,Kondo,Inoue,Kawahata,Jinbo,Sakamoto,Tsukamoto

, p. 94 - 99 (1992)

A series of 8-substituted-9,1-(epoxymethano)-7-fluoro-5-oxo-5H- thiazolo[3,2-a]quinoline-4-carboxylic acids having a novel tetracyclic structure was synthesized and tested for antibacterial activity. The nature of the heteroatom (N, O, or S) substituted a

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