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31202-09-2

2-isopropyl-6-methyl-anisole is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 31202-09-2 Structure

  • Basic information

    1. Product Name: 2-isopropyl-6-methyl-anisole
    2. Synonyms: 2-isopropyl-6-methyl-anisole
    3. CAS NO:31202-09-2
    4. Molecular Formula:
    5. Molecular Weight: 164.247
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 31202-09-2.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-isopropyl-6-methyl-anisole(CAS DataBase Reference)
    10. NIST Chemistry Reference: 2-isopropyl-6-methyl-anisole(31202-09-2)
    11. EPA Substance Registry System: 2-isopropyl-6-methyl-anisole(31202-09-2)

  • 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: 31202-09-2(Hazardous Substances Data)

31202-09-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 31202-09-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,1,2,0 and 2 respectively; the second part has 2 digits, 0 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 31202-09:
(7*3)+(6*1)+(5*2)+(4*0)+(3*2)+(2*0)+(1*9)=52
52 % 10 = 2
So 31202-09-2 is a valid CAS Registry Number.

31202-09-2Relevant articles and documents

Metal triflate-catalyzed cyclization of arylvinylcarbinols: Formal synthesis of (±)-dichroanone and (±)-taiwaniaquinone H

Kakde, Badrinath N.,De, Subhadip,Dey, Dhananjay,Bisai, Alakesh

, p. 8176 - 8179 (2013/09/02)

A formal synthesis of diterpenoids viz. the taiwaniaquinoids (±)-dichroanone (1a) and (±)-taiwaniaquinone H (1b) possessing an all carbon quaternary stereocenter has been reported. The key step involves a metal triflate-catalyzed cyclization of arylvinylc

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