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1,3,4-Thiadiazol-2-ol is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

84352-66-9

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84352-66-9 Usage

Type of Compound

Heterocyclic compound

Structure

Five-membered ring with a sulfur atom, two nitrogen atoms, and an oxygen atom

Bonding

Alternating single and double bonds

Applications

Building block in the synthesis of pharmaceuticals and agrochemicals

Reactivity

Diverse reactivity

Biological Activity

Potential biological activity

Derivatives

Show antioxidant, antimicrobial, and anticancer properties

Importance in Research

Valuable targets in medicinal chemistry research

Intermediates

Important intermediates in the production of functional materials and bioactive compounds

Unique Structure

Versatile reactivity due to the presence of sulfur, nitrogen, and oxygen atoms in the ring structure.

Check Digit Verification of cas no

The CAS Registry Mumber 84352-66-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,4,3,5 and 2 respectively; the second part has 2 digits, 6 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 84352-66:
(7*8)+(6*4)+(5*3)+(4*5)+(3*2)+(2*6)+(1*6)=139
139 % 10 = 9
So 84352-66-9 is a valid CAS Registry Number.

84352-66-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 3H-1,3,4-thiadiazol-2-one

1.2 Other means of identification

Product number -
Other names 3H-[1,3,4]thiadiazol-2-one

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:84352-66-9 SDS

84352-66-9Downstream Products

84352-66-9Relevant academic research and scientific papers

Azo dyes containing 1,3,4-thiadiazole fragment: Synthesis and properties

Amosov, Evgeny,Bagryanskaya, Irina,Karpova, Elena,Selivanova, Galina,Shundrina, Inna,Skolyapova, Alexandrina,Wang, Jiaying

, p. 1929 - 1942 (2022/01/31)

New 1,3,4-thiadiazole derivatives containing a diazenyl group, as well as both a diazenyl and an imino group, were synthesized and their optical and thermal properties were investigated. Initially, new azo compounds containing an azo group directly in the thiadiazole block were obtained by the coupling of diazonium bisulfates based on the previously known 5-derivatives of 2-amino-1,3,4-thiadiazoles with N,N-dialkyl anilines (N(n-Bu)2, NEt2, and NEt(EtOH)). Schiff bases were obtained by the interaction of p-toluidine, p-phenylenediamine and p-aminophenol with azo compounds containing an aldehyde group in the 1,3,4-thiadiazole ring. The new dyes were characterized by spectral (IR, UV, 1H NMR, 13C NMR and mass spectra) and X-ray analyses. This journal is

Process for the preparation of 1,3,4-thiadiazolone derivatives

-

, (2008/06/13)

A process for preparing 1,3,4-thiadiazolone compounds of the formula STR1 comprising reacting a 2-alkoxy-1,3,4-thiadiazole of the formula STR2 with hydrogen chloride in non-aqueous organic solvent under non-aqueous conditions at a temperature of from 0° t

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