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Phenol, 3-chloro-4-[(4-nitrophenyl)thio]- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

104093-36-9

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104093-36-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 104093-36-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,4,0,9 and 3 respectively; the second part has 2 digits, 3 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 104093-36:
(8*1)+(7*0)+(6*4)+(5*0)+(4*9)+(3*3)+(2*3)+(1*6)=89
89 % 10 = 9
So 104093-36-9 is a valid CAS Registry Number.

104093-36-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-chloro-4-(4-nitro-phenylsulfanyl)-phenol

1.2 Other means of identification

Product number -
Other names 3-Chlor-4-(4-nitro-phenylmercapto)-phenol

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:104093-36-9 SDS

104093-36-9Relevant academic research and scientific papers

Quantitative structure-activity relationships in dihydropteroate synthase inhibition by multisubstituted sulfones. Design and synthesis of some new derivatives with improved potency

De Benedetti,Iarossi,Folli,Frassineti,Menziani,Cennamo

, p. 2396 - 2399 (2007/10/02)

On the bases of the linear correlation existing for a training set of homomultisubstituted 4-aminodiphenyl sulfones between the computed (INDO) electronic net charges of the SO2 group and the enzymic inhibition data on dihydropteroate synthase from Escherichia coli, seven new heteromultisubstituted derivatives were designed, synthesized, and tested for their inhibition potencies. These compounds were found to be from 5-11 times more effective than 4,4'-diaminodiphenyl sulfone. The implications of the results in the drug design and in the model for the enzyme-inhibitors interaction are discussed.

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