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1415729-04-2

C24H22ClN5O3 is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1415729-04-2 Structure

  • Basic information

    1. Product Name: C24H22ClN5O3
    2. Synonyms:
    3. CAS NO:1415729-04-2
    4. Molecular Formula:
    5. Molecular Weight: 463.923
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1415729-04-2.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: N/A
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: C24H22ClN5O3(CAS DataBase Reference)
    10. NIST Chemistry Reference: C24H22ClN5O3(1415729-04-2)
    11. EPA Substance Registry System: C24H22ClN5O3(1415729-04-2)

  • 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: 1415729-04-2(Hazardous Substances Data)

1415729-04-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1415729-04-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,4,1,5,7,2 and 9 respectively; the second part has 2 digits, 0 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 1415729-04:
(9*1)+(8*4)+(7*1)+(6*5)+(5*7)+(4*2)+(3*9)+(2*0)+(1*4)=152
152 % 10 = 2
So 1415729-04-2 is a valid CAS Registry Number.

1415729-04-2Downstream Products

1415729-04-2Relevant articles and documents

Heteroaryl urea inhibitors of fatty acid amide hydrolase: Structure-mutagenicity relationships for arylamine metabolites

Tichenor, Mark S.,Keith, John M.,Jones, William M.,Pierce, Joan M.,Merit, Jeff,Hawryluk, Natalie,Seierstad, Mark,Palmer, James A.,Webb, Michael,Karbarz, Mark J.,Wilson, Sandy J.,Wennerholm, Michelle L.,Woestenborghs, Filip,Beerens, Dominiek,Luo, Lin,Brown, Sean M.,Boeck, Marlies De,Chaplan, Sandra R.,Breitenbucher, J. Guy

, p. 7357 - 7362 (2013/02/21)

The structure-activity relationships for a series of heteroaryl urea inhibitors of fatty acid amide hydrolase (FAAH) are described. Members of this class of inhibitors have been shown to inactivate FAAH by covalent modification of an active site serine with subsequent release of an aromatic amine from the urea electrophile. Systematic Ames II testing guided the optimization of urea substituents by defining the structure-mutagenicity relationships for the released aromatic amine metabolites. Potent FAAH inhibitors were identified having heteroaryl amine leaving groups that were non-mutagenic in the Ames II assay.

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