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1579278-31-1

1-(2-(allyloxy)phenyl)-3-bromoprop-2-ynyl acetate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1579278-31-1 Structure

  • Basic information

    1. Product Name: 1-(2-(allyloxy)phenyl)-3-bromoprop-2-ynyl acetate
    2. Synonyms: 1-(2-(allyloxy)phenyl)-3-bromoprop-2-ynyl acetate
    3. CAS NO:1579278-31-1
    4. Molecular Formula:
    5. Molecular Weight: 309.159
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1579278-31-1.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-(2-(allyloxy)phenyl)-3-bromoprop-2-ynyl acetate(CAS DataBase Reference)
    10. NIST Chemistry Reference: 1-(2-(allyloxy)phenyl)-3-bromoprop-2-ynyl acetate(1579278-31-1)
    11. EPA Substance Registry System: 1-(2-(allyloxy)phenyl)-3-bromoprop-2-ynyl acetate(1579278-31-1)

  • 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: 1579278-31-1(Hazardous Substances Data)

1579278-31-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1579278-31-1 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,5,7,9,2,7 and 8 respectively; the second part has 2 digits, 3 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 1579278-31:
(9*1)+(8*5)+(7*7)+(6*9)+(5*2)+(4*7)+(3*8)+(2*3)+(1*1)=221
221 % 10 = 1
So 1579278-31-1 is a valid CAS Registry Number.

1579278-31-1Relevant articles and documents

Regioselective hydration of terminal halo-substituted propargyl carboxylates by gold catalyst: Synthesis of α-acyloxy α'-halo ketones

Ghosh, Nayan,Nayak, Sanatan,Prabagar,Sahoo, Akhila K.

, p. 2453 - 2462 (2014)

Regioselective hydration of the terminal halo-substituted propargyl carboxylate by gold(I) catalyst is reported. The mild catalytic conditions tolerate common acid-labile protecting groups, and a wide variety of α-acyloxy α'-halo ketones are efficiently synthesized within a short reaction time. The α-acyloxy α'-halo ketones are used for the synthesis of 2-aminothiazoles.

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