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Benzoic acid, 4-(3-oxo-2(3H)-isothiazolyl)-, ethyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

26530-26-7

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26530-26-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 26530-26-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,6,5,3 and 0 respectively; the second part has 2 digits, 2 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 26530-26:
(7*2)+(6*6)+(5*5)+(4*3)+(3*0)+(2*2)+(1*6)=97
97 % 10 = 7
So 26530-26-7 is a valid CAS Registry Number.

26530-26-7SDS

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 N-[(4-ethoxycarbonyl)phenyl]isothiazol-3(2H)-one

1.2 Other means of identification

Product number -
Other names KM04416

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:26530-26-7 SDS

26530-26-7Downstream Products

26530-26-7Relevant academic research and scientific papers

Synthesis and antibacterial activity of 2-(4-substituted phenyl)-3(2H)-isothiazolones

Khalaj, Ali,Adibpour, Neda,Shahverdi, Ahmad Reza,Daneshtalab, Mohsen

, p. 699 - 705 (2007/10/03)

Several new and known 2-(4-substituted phenyl)-3(2H)-isothiazolone derivatives with or without chloro substituent at C-5 position were synthesized and their in vitro antibacterial activity against selected Gram-negative and Gram-positive bacteria were eva

A General Synthesis of N-Substituted Isothiazol-3(2H)-ones

Beeley, Nigel R. A.,Harwood, Laurence M.,Hedger, Paul C.

, p. 2245 - 2252 (2007/10/02)

A general route to the synthesis of N-substituted isothiazol-3(2H)-ones (4a-i) is described which proceeds via trichloroacetic acid-mediated ring closure of N-substituted (Z)-3-(benzylsulfinyl)propenamides (15a-i).

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