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(2R,3R)-2,3-epoxy<2,3-H2>oct-4-yn-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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  • 129815-00-5 Structure
  • Basic information

    1. Product Name: (2R,3R)-2,3-epoxy<2,3-H2>oct-4-yn-1-ol
    2. Synonyms: (2R,3R)-2,3-epoxy<2,3-H2>oct-4-yn-1-ol
    3. CAS NO:129815-00-5
    4. Molecular Formula:
    5. Molecular Weight: 142.166
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 129815-00-5.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: (2R,3R)-2,3-epoxy<2,3-H2>oct-4-yn-1-ol(CAS DataBase Reference)
    10. NIST Chemistry Reference: (2R,3R)-2,3-epoxy<2,3-H2>oct-4-yn-1-ol(129815-00-5)
    11. EPA Substance Registry System: (2R,3R)-2,3-epoxy<2,3-H2>oct-4-yn-1-ol(129815-00-5)
  • 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: 129815-00-5(Hazardous Substances Data)

129815-00-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 129815-00-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,9,8,1 and 5 respectively; the second part has 2 digits, 0 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 129815-00:
(8*1)+(7*2)+(6*9)+(5*8)+(4*1)+(3*5)+(2*0)+(1*0)=135
135 % 10 = 5
So 129815-00-5 is a valid CAS Registry Number.

129815-00-5Relevant articles and documents

77. Chiral 2H>-Labelled Methylene Groups in Trienoic- and Dienoic Fatty Acids: a Facile Approach via Asymmetric Epoxidation of 2H>Allyl Alcohols

Neumann, Christoph,Boland, Wilhelm

, p. 754 - 761 (1990)

Chiral 2H>-labelled methylene groups flanked by two double bonds within (poly)unsaturated fatty acids are readily available from trans-2,3-epoxy2H2>alk-4-yn-1-ols, obtained in their turn by asymmetric epoxidation of the corresp

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