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36874-52-9

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36874-52-9 Usage

Appearance

Yellow to orange powder

Type

Oxime derivative of 1,2-propanedione (acetylacetone)

Industrial Applications

Chelating agent for various metal ions
Stabilizer in industrial processes

Pharmaceutical Potential

Studied for its potential use in pharmaceuticals

Environmental Applications

Investigated as a fluorescent probe for detecting heavy metal ions in environmental samples

Health and Disease

Researched for its role in inhibiting the production of advanced glycation end products, which are associated with aging and various diseases

Ongoing Research

Subject of ongoing research and development in different fields

Chemical Structure

Contains a benzothiazole ring, a carbonyl group, and an oxime functional group

Check Digit Verification of cas no

The CAS Registry Mumber 36874-52-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,6,8,7 and 4 respectively; the second part has 2 digits, 5 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 36874-52:
(7*3)+(6*6)+(5*8)+(4*7)+(3*4)+(2*5)+(1*2)=149
149 % 10 = 9
So 36874-52-9 is a valid CAS Registry Number.

36874-52-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-(benzothiazol-2-yl)-1-hydroxyimino-2-propanone

1.2 Other means of identification

Product number -
Other names 1-Benzothiazol-2-yl-propan-1,2-dion-1-oxim

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:36874-52-9 SDS

36874-52-9Downstream Products

36874-52-9Relevant articles and documents

Synthesis of 3-(6-R-benzothiazol-2-yl)-4-methyl-1,2,5-oxadiazoles

Britsun,Borisevich,Samoilenko,Lozinskii

, p. 745 - 747 (2005)

The nitrosation of N-aryl-3-oxobutanethioamides afforded 1-(6-R-benzothiasol-2-yl)-1-hydroxyimino-2-propanones that at oximation with hydroxylamine were converted into 1-(6-R-benzothiazol-2-yl)-1,2- dihydroxyiminopropanes. The latter were dehydrated by he

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