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203441-65-0

1-Benzyl-3-methyl-1H-indole-6-carboxylic acid is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 203441-65-0 Structure

  • Basic information

    1. Product Name: 1-Benzyl-3-methyl-1H-indole-6-carboxylic acid
    2. Synonyms: 1-Benzyl-3-methyl-1H-indole-6-carboxylic acid
    3. CAS NO:203441-65-0
    4. Molecular Formula:
    5. Molecular Weight: 265.312
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 203441-65-0.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: 1-Benzyl-3-methyl-1H-indole-6-carboxylic acid(CAS DataBase Reference)
    10. NIST Chemistry Reference: 1-Benzyl-3-methyl-1H-indole-6-carboxylic acid(203441-65-0)
    11. EPA Substance Registry System: 1-Benzyl-3-methyl-1H-indole-6-carboxylic acid(203441-65-0)

  • 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: 203441-65-0(Hazardous Substances Data)

203441-65-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 203441-65-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,0,3,4,4 and 1 respectively; the second part has 2 digits, 6 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 203441-65:
(8*2)+(7*0)+(6*3)+(5*4)+(4*4)+(3*1)+(2*6)+(1*5)=90
90 % 10 = 0
So 203441-65-0 is a valid CAS Registry Number.

203441-65-0Downstream Products

203441-65-0Relevant articles and documents

Orally active indole N-oxide PDE4 inhibitors

Hulme, Christopher,Mathew, Rose,Moriarty, Kevin,Miller, Bruce,Ramanjulu, Mercy,Cox, Paul,Souness, John,Page, Ken M.,Uhl, Joanne,Travis, Jeffrey,Labaudiniere, Richard,Huang, Fu-Chih,Djuric, Stevan W.

, p. 3053 - 3058 (2007/10/03)

This communication describes the synthesis and in vitro and in vivo evaluation of a novel potent series of phosphodiesterase type (IV) (PDE4) inhibitors. Several of the compounds presented possess low nanomolar IC50's for PDE4 inhibition and excellent in vivo activity for inhibition of TNF-α levels in LPS challenged mice (mouse endotoxemia model). Emesis studies (dog) and efficacy in a SCW arthritis model for the most potent PDE4 inhibitors are presented.

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