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2-phenyl-2-(prop-2-ynyl)oxirane is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 20131-24-2 Structure
  • Basic information

    1. Product Name: 2-phenyl-2-(prop-2-ynyl)oxirane
    2. Synonyms: 2-phenyl-2-(prop-2-ynyl)oxirane
    3. CAS NO:20131-24-2
    4. Molecular Formula:
    5. Molecular Weight: 158.2
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 20131-24-2.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: 2-phenyl-2-(prop-2-ynyl)oxirane(CAS DataBase Reference)
    10. NIST Chemistry Reference: 2-phenyl-2-(prop-2-ynyl)oxirane(20131-24-2)
    11. EPA Substance Registry System: 2-phenyl-2-(prop-2-ynyl)oxirane(20131-24-2)
  • 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: 20131-24-2(Hazardous Substances Data)

20131-24-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 20131-24-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,0,1,3 and 1 respectively; the second part has 2 digits, 2 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 20131-24:
(7*2)+(6*0)+(5*1)+(4*3)+(3*1)+(2*2)+(1*4)=42
42 % 10 = 2
So 20131-24-2 is a valid CAS Registry Number.

20131-24-2Downstream Products

20131-24-2Relevant articles and documents

Efficient synthetic method for the preparation of allyl- and propargyl-epoxides by allylation and propargylation of α-haloketones with organozinc reagents

Pan, Jie,Zhang, Min,Zhang, Songlin

experimental part, p. 1060 - 1067 (2012/04/10)

A simple, efficient, and non-metal catalyzed synthetic method for the preparation of substituted allyl- and propargyl-epoxides by allylation and propargylation of α-halo ketones with organozinc reagents in mild conditions is reported in this paper. The present method complements the existing synthetic methods due to some advantageous properties of the organozinc reagents such as availability, selectivity, operational simplicity and low toxicity.

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