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87512-65-0

2-(1-isobutylprop-2-enyl)phenol is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 87512-65-0 Structure

  • Basic information

    1. Product Name: 2-(1-isobutylprop-2-enyl)phenol
    2. Synonyms: 2-(1-isobutylprop-2-enyl)phenol
    3. CAS NO:87512-65-0
    4. Molecular Formula:
    5. Molecular Weight: 190.285
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 87512-65-0.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: 2-(1-isobutylprop-2-enyl)phenol(CAS DataBase Reference)
    10. NIST Chemistry Reference: 2-(1-isobutylprop-2-enyl)phenol(87512-65-0)
    11. EPA Substance Registry System: 2-(1-isobutylprop-2-enyl)phenol(87512-65-0)

  • 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: 87512-65-0(Hazardous Substances Data)

87512-65-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 87512-65-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,7,5,1 and 2 respectively; the second part has 2 digits, 6 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 87512-65:
(7*8)+(6*7)+(5*5)+(4*1)+(3*2)+(2*6)+(1*5)=150
150 % 10 = 0
So 87512-65-0 is a valid CAS Registry Number.

87512-65-0Downstream Products

87512-65-0Relevant articles and documents

The Behaviour of 2H-1-Benzopyrans Toward Trialkylaluminium Reagents

Alberola, Angel,Ortega, Alfonso Gonzalez,Pedrosa, Rafael,Bragado, Jose L. Perez,Amo, Justo F. Rodriguez

, p. 1209 - 1212 (2007/10/02)

2H-1-Benzopyrans react with trialkylaluminium compounds by alkyl- and hydrogen-transfer to C-2 and C-4 to give the o-allylphenols (2), (3), and the (E)-o-propenylphenols (4) and (5).The site of attack and the ratio of alkyl- to hydrogen-transfer depend on the alkylaluminium used and on the size of the substituent at C-2 of the pyran.A mechanism involving reaction of the alkylaluminium with the quinone methanide (6), which is in equilibrium with the pyran (1), is in accord with all experimental results.

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