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4341-57-5

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4341-57-5 Usage

Organic compound

Contains an indole ring

Substitution

Iodo group and carbonyl group

Potential applications

Pharmaceutical field

Building block

Synthesis of various bioactive molecules

Functional groups

Hydrazine and carbothioamide

Versatility

Potential for further chemical manipulations and derivatization

Importance in medicinal chemistry research

Can serve as a starting point for the development of new drugs and bioactive compounds

Check Digit Verification of cas no

The CAS Registry Mumber 4341-57-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,3,4 and 1 respectively; the second part has 2 digits, 5 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 4341-57:
(6*4)+(5*3)+(4*4)+(3*1)+(2*5)+(1*7)=75
75 % 10 = 5
So 4341-57-5 is a valid CAS Registry Number.

4341-57-5SDS

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 [(5-iodo-2-oxoindol-3-yl)amino]thiourea

1.2 Other means of identification

Product number -
Other names -

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:4341-57-5 SDS

4341-57-5Downstream Products

4341-57-5Relevant articles and documents

Synthesis and evaluation of isatins and thiosemicarbazone derivatives against cruzain, falcipain-2 and rhodesain

Chiyanzu, Idan,Hansell, Elizabeth,Gut, Jiri,Rosenthal, Philip J.,McKerrow, James H.,Chibale, Kelly

, p. 3527 - 3530 (2007/10/03)

While commercial isatins were practically inactive against the target proteases, thiosemicarbazone derivatives were found to be active. The most active compound from the series displayed an inhibitory IC50 value of 1 μM against rhodesain. One thiosemicarbazone was found to be active against all three proteases with inhibitory IC50 values of 10 μM or less. A combination of N-benzylation and appropriate substitution on the aromatic portion of the isatin scaffold was generally found to be beneficial especially against cruzain for ketone inhibitors.

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