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4614-21-5

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4614-21-5 Usage

Type of compound

Heterocyclic aromatic compound

Structure

Contains a benzothiazole ring and a ketone functional group

Substituent

Attached to a phenylethyl substituent

Potential applications

Pharmaceuticals and organic synthesis

Biological activities

Possesses interesting biological activities

Synthesis use

Can be used as a building block for the synthesis of various organic compounds

Versatility

Unique structure and reactivity

Scientific and industrial applications

Potential uses in various fields

Check Digit Verification of cas no

The CAS Registry Mumber 4614-21-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,6,1 and 4 respectively; the second part has 2 digits, 2 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 4614-21:
(6*4)+(5*6)+(4*1)+(3*4)+(2*2)+(1*1)=75
75 % 10 = 5
So 4614-21-5 is a valid CAS Registry Number.

4614-21-5SDS

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 3-phenacyl-1,3-benzothiazol-2-one

1.2 Other means of identification

Product number -
Other names 2-Oxo-N-phenacyl-benzthiazolin

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:4614-21-5 SDS

4614-21-5Downstream Products

4614-21-5Relevant articles and documents

ALKYLATION OF 2-HYDROXYBENZOTHIAZOLE SALTS

Collina, Gianni,Forlani, Luciano,Mezzina, Elisabetta,Sintoni, Marina,Todesco, Paolo E.

, p. 281 - 286 (2007/10/02)

The alkylation reactions of 2-hydroxybenzothiazole salts with various alkyl halides afford the N-alkylated derivatives.With alkyl halides prone to molecular reactions, 2-hydroxybenzothiazole in the presence of silver carbonate, yields N- and O-alkylated p

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