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5728-12-1

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5728-12-1 Usage

Chemical class

Thiadiazole derivatives

Common use

Building block in the synthesis of pharmaceutical compounds and agrochemicals

Biological activities

Anti-inflammatory, anti-tumor, and anti-bacterial

Preclinical studies

Shown potential as an agent in various biological activities

Structure and reactivity

Unique, making it an important intermediate in the production of advanced materials and fine chemicals

Investigation

Potential application in the development of new drugs for the treatment of various diseases

Check Digit Verification of cas no

The CAS Registry Mumber 5728-12-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,7,2 and 8 respectively; the second part has 2 digits, 1 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 5728-12:
(6*5)+(5*7)+(4*2)+(3*8)+(2*1)+(1*2)=101
101 % 10 = 1
So 5728-12-1 is a valid CAS Registry Number.

5728-12-1SDS

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 4-phenyl-1,2,5-thiadiazol-3-one

1.2 Other means of identification

Product number -
Other names 3-hydroxy-4-phenyl-1,2,5-thiadiazole

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:5728-12-1 SDS

5728-12-1Relevant articles and documents

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Mizsak,Perelman

, p. 1964 (1966)

-

Sulfamates as antiglaucoma agents

-

, (2008/06/13)

Sulfamate esters of the formula where A is aryloxyalkyl, p is the number of unreacted hydroxy groups present on the alkyl moiety and may be zero, z is the number of --OS(O)2 NR1 R2 groups attached to carbons of the alkyl moiety and is always at least one; R1 and R2 are selected from hydrogen, loweralkyl, carboxy, and the like are useful in treating glaucoma.

FACILE SYNTHESIS OF 3-OXO-1,2,5-THIADIAZOLES; 7β-CEPHALOSPHORINS

Lunn, W. H. W.,Shadle, J. K.

, p. 8615 - 8620 (2007/10/02)

A simple procedure is described for the preparation of 3-oxo-1,2,5-thiadiazoles under mild conditions.This procedure has provided hitherto unknown 7β-3-oxo-1,2,5-thiadiazol-2-yl)cephalosporins.

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