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100975-75-5

2-(4-benzylphenyl)ethan-1-ol is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 100975-75-5 Structure

  • Basic information

    1. Product Name: 2-(4-benzylphenyl)ethan-1-ol
    2. Synonyms:
    3. CAS NO:100975-75-5
    4. Molecular Formula:
    5. Molecular Weight: 212.291
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 100975-75-5.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-(4-benzylphenyl)ethan-1-ol(CAS DataBase Reference)
    10. NIST Chemistry Reference: 2-(4-benzylphenyl)ethan-1-ol(100975-75-5)
    11. EPA Substance Registry System: 2-(4-benzylphenyl)ethan-1-ol(100975-75-5)

  • 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: 100975-75-5(Hazardous Substances Data)

100975-75-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 100975-75-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,0,9,7 and 5 respectively; the second part has 2 digits, 7 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 100975-75:
(8*1)+(7*0)+(6*0)+(5*9)+(4*7)+(3*5)+(2*7)+(1*5)=115
115 % 10 = 5
So 100975-75-5 is a valid CAS Registry Number.

100975-75-5Relevant articles and documents

An Efficient Ga(OTf)3/Isopropanol Catalytic System for Direct Reduction of Benzylic Alcohols

Sai, Masahiro

, p. 4330 - 4335 (2018)

This study aims to report the first gallium-catalyzed direct reduction of benzylic alcohols using isopropanol as a reductant. The reaction proceeds via gallium catalyst-assisted hydride transfer of the in situ-generated benzylic isopropyl ether. The method generates only water and acetone as byproducts and thus provides an atom-economic and environmentally friendly approach to the synthesis of di- and triarylmethanes, which are important substructures in various bioactive compounds and functional materials. (Figure presented.).

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