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5-Benzyl-4-isopropylidene-2,2-dimethyl-3,4-dihydro-2H-pyrrole is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 76528-08-0 Structure
  • Basic information

    1. Product Name: 5-Benzyl-4-isopropylidene-2,2-dimethyl-3,4-dihydro-2H-pyrrole
    2. Synonyms:
    3. CAS NO:76528-08-0
    4. Molecular Formula:
    5. Molecular Weight: 227.349
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 76528-08-0.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: 5-Benzyl-4-isopropylidene-2,2-dimethyl-3,4-dihydro-2H-pyrrole(CAS DataBase Reference)
    10. NIST Chemistry Reference: 5-Benzyl-4-isopropylidene-2,2-dimethyl-3,4-dihydro-2H-pyrrole(76528-08-0)
    11. EPA Substance Registry System: 5-Benzyl-4-isopropylidene-2,2-dimethyl-3,4-dihydro-2H-pyrrole(76528-08-0)
  • 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: 76528-08-0(Hazardous Substances Data)

76528-08-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 76528-08-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,6,5,2 and 8 respectively; the second part has 2 digits, 0 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 76528-08:
(7*7)+(6*6)+(5*5)+(4*2)+(3*8)+(2*0)+(1*8)=150
150 % 10 = 0
So 76528-08-0 is a valid CAS Registry Number.

76528-08-0Downstream Products

76528-08-0Relevant articles and documents

The Ritter reaction in the synthesis of ortho-fused nitrogen-containing heterocycles

Shome,Smith,Southam,Oxford

, p. 2927 - 2930 (2007/10/02)

The acid-catalysed condensation of a 1,4- and a 1,5-ditertiary diol with various arylated nitriles is shown to provide a simple and novel route to reduced benz[f]indoles, naphth[1,8a,8-fg]indoles, benzo[4,5]cyclohepta[1,2-b]pyrroles, and benzo[g]quinoline

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