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1-Benzyl-1H,4H,5H,6H-cyclopenta[b]pyrrole-2-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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  • 164736-53-2 Structure
  • Basic information

    1. Product Name: 1-Benzyl-1H,4H,5H,6H-cyclopenta[b]pyrrole-2-carboxylic acid
    2. Synonyms: 1-Benzyl-1H,4H,5H,6H-cyclopenta[b]pyrrole-2-carboxylic acid
    3. CAS NO:164736-53-2
    4. Molecular Formula: C15H15NO2
    5. Molecular Weight: 241.2851
    6. EINECS: 936-631-1
    7. Product Categories: N/A
    8. Mol File: 164736-53-2.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: 1-Benzyl-1H,4H,5H,6H-cyclopenta[b]pyrrole-2-carboxylic acid(CAS DataBase Reference)
    10. NIST Chemistry Reference: 1-Benzyl-1H,4H,5H,6H-cyclopenta[b]pyrrole-2-carboxylic acid(164736-53-2)
    11. EPA Substance Registry System: 1-Benzyl-1H,4H,5H,6H-cyclopenta[b]pyrrole-2-carboxylic acid(164736-53-2)
  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: IRRITANT
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 164736-53-2(Hazardous Substances Data)

164736-53-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 164736-53-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,6,4,7,3 and 6 respectively; the second part has 2 digits, 5 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 164736-53:
(8*1)+(7*6)+(6*4)+(5*7)+(4*3)+(3*6)+(2*5)+(1*3)=152
152 % 10 = 2
So 164736-53-2 is a valid CAS Registry Number.

164736-53-2Downstream Products

164736-53-2Relevant articles and documents

Cyclopentaindoles. Part 2. Model studies towards the tremorgenic mycotoxins

Harrison, Carrie-Ann,Jackson, P. Mark,Moody, Christopher J.,Williams, Jonathan M. J.

, p. 1131 - 1136 (2007/10/02)

The 7-bromocyclopentaindole 3 has been converted into the hydroxybutenyl derivatives 5 and 6, and the tetrahydrofuranylidene derivative 8 in model studies towards the elaboration of paspalitrem and lolitrem type side chains.In a parallel approach, the cyclopentapyrrole 13 was converted into the fused α-pyrone 16 which acted as a pyrrole-2,3-quinodimethane, and underwent Diels-Alder reaction to give, after loss of carbon dioxide, the cyclopentaindoles 17 - 21.

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