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CAS

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135520-26-2

2-Methylene-cyclopentanecarboxylic acid methyl-phenyl-amide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 135520-26-2 Structure

  • Basic information

    1. Product Name: 2-Methylene-cyclopentanecarboxylic acid methyl-phenyl-amide
    2. Synonyms:
    3. CAS NO:135520-26-2
    4. Molecular Formula:
    5. Molecular Weight: 215.295
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 135520-26-2.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: 2-Methylene-cyclopentanecarboxylic acid methyl-phenyl-amide(CAS DataBase Reference)
    10. NIST Chemistry Reference: 2-Methylene-cyclopentanecarboxylic acid methyl-phenyl-amide(135520-26-2)
    11. EPA Substance Registry System: 2-Methylene-cyclopentanecarboxylic acid methyl-phenyl-amide(135520-26-2)

  • 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: 135520-26-2(Hazardous Substances Data)

135520-26-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 135520-26-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,5,5,2 and 0 respectively; the second part has 2 digits, 2 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 135520-26:
(8*1)+(7*3)+(6*5)+(5*5)+(4*2)+(3*0)+(2*2)+(1*6)=102
102 % 10 = 2
So 135520-26-2 is a valid CAS Registry Number.

135520-26-2Downstream Products

135520-26-2Relevant articles and documents

Radical Translocation Reactions of o-Iodoanilides: The Use of Carbon-Hydrogen Bonds as Precursors of Radicals Adjacent to Carbonyl Groups

Curran, Dennis P.,Abraham, Ann C.,Liu, Hongtao

, p. 4335 - 4337 (2007/10/02)

The treatment of o-iodoanilides with tributyltin hydride results in radical generation followed by rapid translocation to produce radicals adjacent to carbonyls.These radicals participate in cyclization and asymmetric addition reactions.

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