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143703-96-2

3,7-dimethyl-7-(4-methoxyphenyl)-1-octanol is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 143703-96-2 Structure

  • Basic information

    1. Product Name: 3,7-dimethyl-7-(4-methoxyphenyl)-1-octanol
    2. Synonyms: 3,7-dimethyl-7-(4-methoxyphenyl)-1-octanol
    3. CAS NO:143703-96-2
    4. Molecular Formula:
    5. Molecular Weight: 264.408
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 143703-96-2.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: 3,7-dimethyl-7-(4-methoxyphenyl)-1-octanol(CAS DataBase Reference)
    10. NIST Chemistry Reference: 3,7-dimethyl-7-(4-methoxyphenyl)-1-octanol(143703-96-2)
    11. EPA Substance Registry System: 3,7-dimethyl-7-(4-methoxyphenyl)-1-octanol(143703-96-2)

  • 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: 143703-96-2(Hazardous Substances Data)

143703-96-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 143703-96-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,3,7,0 and 3 respectively; the second part has 2 digits, 9 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 143703-96:
(8*1)+(7*4)+(6*3)+(5*7)+(4*0)+(3*3)+(2*9)+(1*6)=122
122 % 10 = 2
So 143703-96-2 is a valid CAS Registry Number.

143703-96-2Downstream Products

143703-96-2Relevant articles and documents

AlCl3-N,N-Dimethylaniline: A Novel Benzyl and Allyl Ether Cleavage Reagent

Akiyama, Takahiko,Hirofuji, Hajimu,Ozaki, Shoichiro

, p. 1932 - 1938 (1992)

A combination system of AlCl3-N,N-dimethylaniline was found to cleave benzyl ethers readily to give parent alcohols in excellent yields.The system also cleaved allyl as well as methyl ethers.Numerous functional groups such as benzoyloxy, phenylthio, and olefinic double bond were not affected.Comparison of AlCl3-N,N-dimethylaniline and AlCl3-anisole were described.

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