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53068-24-9

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53068-24-9 Usage

General Description

4-(3,4-DIMETHOXYPHENETHYL)-3-THIOSEMICARBAZIDE is a chemical compound with the molecular formula C11H17N3O2S. It is a thiosemicarbazide derivative with potential pharmacological properties. 4-(3,4-DIMETHOXYPHENETHYL)-3-THIOSEMICARBAZIDE has been studied for its potential antifungal and antibacterial activities. Thiosemicarbazides have been investigated for their potential as antimicrobial, anticancer, and antitubercular agents. 4-(3,4-DIMETHOXYPHENETHYL)-3-THIOSEMICARBAZIDE may represent a potential lead compound for further development of novel pharmaceutical agents with therapeutic applications.

Check Digit Verification of cas no

The CAS Registry Mumber 53068-24-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,3,0,6 and 8 respectively; the second part has 2 digits, 2 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 53068-24:
(7*5)+(6*3)+(5*0)+(4*6)+(3*8)+(2*2)+(1*4)=109
109 % 10 = 9
So 53068-24-9 is a valid CAS Registry Number.
InChI:InChI=1/C11H17N3O2S/c1-15-9-4-3-8(7-10(9)16-2)5-6-13-11(17)14-12/h3-4,7H,5-6,12H2,1-2H3,(H2,13,14,17)

53068-24-9SDS

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 1-amino-3-[2-(3,4-dimethoxyphenyl)ethyl]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

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Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:53068-24-9 SDS

53068-24-9Relevant articles and documents

Synthesis and optimization of thiadiazole derivatives as a novel class of substrate competitive c-Jun N-terminal kinase inhibitors

De, Surya K.,Chen, Vida,Stebbins, John L.,Chen, Li-Hsing,Cellitti, Jason F.,Machleidt, Thomas,Barile, Elisa,Riel-Mehan, Megan,Dahl, Russell,Yang, Li,Emdadi, Aras,Murphy, Ria,Pellecchia, Maurizio

scheme or table, p. 590 - 596 (2010/05/02)

A series of thiadiazole derivatives has been designed as potential allosteric, substrate competitive inhibitors of the protein kinase JNK. We report on the synthesis, characterization and evaluation of a series of compounds that resulted in the identifica

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