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N-phenyl-2-(3-phenylpropanoyl)hydrazinecarbothioamide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 292644-08-7 Structure
  • Basic information

    1. Product Name: N-phenyl-2-(3-phenylpropanoyl)hydrazinecarbothioamide
    2. Synonyms: N-phenyl-2-(3-phenylpropanoyl)hydrazinecarbothioamide
    3. CAS NO:292644-08-7
    4. Molecular Formula: C16H17N3OS
    5. Molecular Weight: 299.39068
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 292644-08-7.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: N-phenyl-2-(3-phenylpropanoyl)hydrazinecarbothioamide(CAS DataBase Reference)
    10. NIST Chemistry Reference: N-phenyl-2-(3-phenylpropanoyl)hydrazinecarbothioamide(292644-08-7)
    11. EPA Substance Registry System: N-phenyl-2-(3-phenylpropanoyl)hydrazinecarbothioamide(292644-08-7)
  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 292644-08-7(Hazardous Substances Data)

292644-08-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 292644-08-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,9,2,6,4 and 4 respectively; the second part has 2 digits, 0 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 292644-08:
(8*2)+(7*9)+(6*2)+(5*6)+(4*4)+(3*4)+(2*0)+(1*8)=157
157 % 10 = 7
So 292644-08-7 is a valid CAS Registry Number.

292644-08-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-phenyl-3-(3-phenylpropanoylamino)thiourea

1.2 Other means of identification

Product number -
Other names N-phenyl-2-(3-phenylpropanoyl)hydrazinecarbothioamide

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:292644-08-7 SDS

292644-08-7Relevant articles and documents

Alkylsulfanyl-1,2,4-triazoles, a New Class of allosteric valosine containing protein inhibitors. Synthesis and structure-activity relationships

Polucci, Paolo,Magnaghi, Paola,Angiolini, Mauro,Asa, Daniela,Avanzi, Nilla,Badari, Alessandra,Bertrand, Jay,Casale, Elena,Cauteruccio, Silvia,Cirla, Alessandra,Cozzi, Liviana,Galvani, Arturo,Jackson, Peter K.,Liu, Yichin,Magnuson, Steven,Malgesini, Beatrice,Nuvoloni, Stefano,Orrenius, Christian,Sirtori, Federico Riccardi,Riceputi, Laura,Rizzi, Simona,Trucchi, Beatrice,O'Brien, Tom,Isacchi, Antonella,Donati, Daniele,D'Alessio, Roberto

, p. 437 - 450 (2013/04/10)

Valosine containing protein (VCP), also known as p97, is a member of AAA ATPase family that is involved in several biological processes and plays a central role in the ubiquitin-mediated degradation of misfolded proteins. VCP is an ubiquitously expressed, highly abundant protein and has been found overexpressed in many tumor types, sometimes associated with poor prognosis. In this respect, VCP has recently received a great deal of attention as a potential new target for cancer therapy. In this paper, the discovery and structure-activity relationships of alkylsulfanyl-1,2,4-triazoles, a new class of potent, allosteric VCP inhibitors, are described. Medicinal chemistry manipulation of compound 1, identified via HTS, led to the discovery of potent and selective inhibitors with submicromolar activity in cells and clear mechanism of action at consistent doses. This represents a first step toward a new class of potential anticancer agents.

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