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CAS

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124601-03-2

1-phenylhex-1-en-5-yn-3-ol is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 124601-03-2 Structure

  • Basic information

    1. Product Name: 1-phenylhex-1-en-5-yn-3-ol
    2. Synonyms:
    3. CAS NO:124601-03-2
    4. Molecular Formula:
    5. Molecular Weight: 172.227
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 124601-03-2.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: 1-phenylhex-1-en-5-yn-3-ol(CAS DataBase Reference)
    10. NIST Chemistry Reference: 1-phenylhex-1-en-5-yn-3-ol(124601-03-2)
    11. EPA Substance Registry System: 1-phenylhex-1-en-5-yn-3-ol(124601-03-2)

  • 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: 124601-03-2(Hazardous Substances Data)

124601-03-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 124601-03-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,4,6,0 and 1 respectively; the second part has 2 digits, 0 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 124601-03:
(8*1)+(7*2)+(6*4)+(5*6)+(4*0)+(3*1)+(2*0)+(1*3)=82
82 % 10 = 2
So 124601-03-2 is a valid CAS Registry Number.

124601-03-2Downstream Products

124601-03-2Relevant articles and documents

Indium-mediated asymmetric Barbier-type propargylations: Additions to aldehydes and ketones and mechanistic investigation of the organoindium reagents

Haddad, Terra D.,Hirayama, Lacie C.,Buckley, Jannise J.,Singaram, Bakthan

, p. 889 - 898 (2012)

We report a simple, efficient, and general method for the indium-mediated enantioselective propargylation of aromatic and aliphatic aldehydes under Barbier-type conditions in a one-pot synthesis affording the corresponding chiral alcohol products in very

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