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857953-36-7

Acetanilide, N-1-methyleneallyl- (5CI) is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 857953-36-7 Structure

  • Basic information

    1. Product Name: Acetanilide, N-1-methyleneallyl- (5CI)
    2. Synonyms: Acetanilide, N-1-methyleneallyl- (5CI)
    3. CAS NO:857953-36-7
    4. Molecular Formula: C12H13NO
    5. Molecular Weight: 187.23772
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 857953-36-7.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: Acetanilide, N-1-methyleneallyl- (5CI)(CAS DataBase Reference)
    10. NIST Chemistry Reference: Acetanilide, N-1-methyleneallyl- (5CI)(857953-36-7)
    11. EPA Substance Registry System: Acetanilide, N-1-methyleneallyl- (5CI)(857953-36-7)

  • 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: 857953-36-7(Hazardous Substances Data)

857953-36-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 857953-36-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,5,7,9,5 and 3 respectively; the second part has 2 digits, 3 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 857953-36:
(8*8)+(7*5)+(6*7)+(5*9)+(4*5)+(3*3)+(2*3)+(1*6)=227
227 % 10 = 7
So 857953-36-7 is a valid CAS Registry Number.

857953-36-7Downstream Products

857953-36-7Relevant articles and documents

Synthesis of 2-Amino-1,3-dienes from Propargyl Carbonates via Palladium-Catalyzed Carbon-Nitrogen Bond Formation

O'Broin, Calvin Q.,Guiry, Patrick J.

, p. 879 - 883 (2020)

A catalytic method to synthesize 1,3,-dienes from propargylic precursors is reported. This palladium-catalyzed carbon-nitrogen bond-forming reaction furnishes 2-amino-1,3-dienes in excellent yields (up to 98%) and shows a broad tolerance to functional group diversity. The reaction has been demonstrated for over 30 amine substrates, including anilines and indoles, and proceeds under mild neutral conditions. The resulting 1,3-dienes are of great synthetic interest because of their further reaction potential.

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