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CAS

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127311-26-6

Phenol, 2,6-dimethyl-4-(3-phenylpropyl)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 127311-26-6 Structure

  • Basic information

    1. Product Name: Phenol, 2,6-dimethyl-4-(3-phenylpropyl)-
    2. Synonyms:
    3. CAS NO:127311-26-6
    4. Molecular Formula: C17H20O
    5. Molecular Weight: 240.345
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 127311-26-6.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: Phenol, 2,6-dimethyl-4-(3-phenylpropyl)-(CAS DataBase Reference)
    10. NIST Chemistry Reference: Phenol, 2,6-dimethyl-4-(3-phenylpropyl)-(127311-26-6)
    11. EPA Substance Registry System: Phenol, 2,6-dimethyl-4-(3-phenylpropyl)-(127311-26-6)

  • 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: 127311-26-6(Hazardous Substances Data)

127311-26-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 127311-26-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,7,3,1 and 1 respectively; the second part has 2 digits, 2 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 127311-26:
(8*1)+(7*2)+(6*7)+(5*3)+(4*1)+(3*1)+(2*2)+(1*6)=96
96 % 10 = 6
So 127311-26-6 is a valid CAS Registry Number.

127311-26-6Relevant articles and documents

Formal Cycloaddition of Benzylic Cations with Alkenes

Angle, Steven R.,Arnaiz, Damian O.

, p. 5937 - 5947 (1992)

The reaction of benzylic cations with styrenes affords dihydro(1H)indenes in good yield via a formal atom cycloadditon.The cations were generated from quinone methides and benzylic alcohols. (E)-Styrenes participate in the reaction with remarkable stereoselectivity affording dihydro(1H)indenes with three stereogenic centers with >40:1 diastereoselectivity.A possible transition state for the reaction is discussed.Less activated alkenes such as dihydropyran and methylcyclohexane afforded cycloadducts in 66percent and 51percent yields, respectively.

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