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CAS

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31573-16-7

2-(2-methoxy-4-methylphenyl)-6-methylhept-5-en-2-ol is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 31573-16-7 Structure

  • Basic information

    1. Product Name: 2-(2-methoxy-4-methylphenyl)-6-methylhept-5-en-2-ol
    2. Synonyms: 2-(2-methoxy-4-methylphenyl)-6-methylhept-5-en-2-ol
    3. CAS NO:31573-16-7
    4. Molecular Formula:
    5. Molecular Weight: 248.365
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 31573-16-7.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-(2-methoxy-4-methylphenyl)-6-methylhept-5-en-2-ol(CAS DataBase Reference)
    10. NIST Chemistry Reference: 2-(2-methoxy-4-methylphenyl)-6-methylhept-5-en-2-ol(31573-16-7)
    11. EPA Substance Registry System: 2-(2-methoxy-4-methylphenyl)-6-methylhept-5-en-2-ol(31573-16-7)

  • 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: 31573-16-7(Hazardous Substances Data)

31573-16-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 31573-16-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,1,5,7 and 3 respectively; the second part has 2 digits, 1 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 31573-16:
(7*3)+(6*1)+(5*5)+(4*7)+(3*3)+(2*1)+(1*6)=97
97 % 10 = 7
So 31573-16-7 is a valid CAS Registry Number.

31573-16-7Relevant articles and documents

Total Synthesis of (-)-Bacchopetiolone via an Asymmetric Hydroxylative Phenol Dearomatization/[4+2]-Dimerization Cascade Promoted by a Novel Salen-Type Chiral Iodane

Coffinier, Romain,Assal, Mourad El,Peixoto, Philippe A.,Bosset, Cyril,Miqueu, Karinne,Sotiropoulos, Jean-Marc,Pouységu, Laurent,Quideau, Stéphane

supporting information, p. 1120 - 1123 (2016/03/15)

The first total and biomimetic synthesis of the natural bis(sesquiterpene) (-)-bacchopetiolone (revised structure) was completed through a highly diastereoselective hydroxylative phenol dearomatization/[4+2]-dimerization cascade conversion of (+)-curcuphe

Efficient total synthesis of racemic bisabolane sesquiterpenes curcuphenol and xanthorrhizol starting from substituted acetophenones

Montiel, Luisa E.,Zepeda, L. Gerardo,Tamariz, Joaquin

experimental part, p. 1261 - 1273 (2010/09/07)

A total synthesis of natural bisabolane sesquiterpenes curcuphenol (1) and xanthorrhizol (2) was developed by using the substituted acetophenones 4 and 5, respectively, as starting materials. The acetyl group of the latter was activated through ethoxycarb

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