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1036999-71-9

N-(4-benzoylphenyl)-2-(hydroxymethyl)-N-methylacrylamide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1036999-71-9 Structure

  • Basic information

    1. Product Name: N-(4-benzoylphenyl)-2-(hydroxymethyl)-N-methylacrylamide
    2. Synonyms: N-(4-benzoylphenyl)-2-(hydroxymethyl)-N-methylacrylamide
    3. CAS NO:1036999-71-9
    4. Molecular Formula:
    5. Molecular Weight: 295.338
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1036999-71-9.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: N-(4-benzoylphenyl)-2-(hydroxymethyl)-N-methylacrylamide(CAS DataBase Reference)
    10. NIST Chemistry Reference: N-(4-benzoylphenyl)-2-(hydroxymethyl)-N-methylacrylamide(1036999-71-9)
    11. EPA Substance Registry System: N-(4-benzoylphenyl)-2-(hydroxymethyl)-N-methylacrylamide(1036999-71-9)

  • 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: 1036999-71-9(Hazardous Substances Data)

1036999-71-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1036999-71-9 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,3,6,9,9 and 9 respectively; the second part has 2 digits, 7 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 1036999-71:
(9*1)+(8*0)+(7*3)+(6*6)+(5*9)+(4*9)+(3*9)+(2*7)+(1*1)=189
189 % 10 = 9
So 1036999-71-9 is a valid CAS Registry Number.

1036999-71-9Relevant articles and documents

Photochemical electrocyclization of α,β-unsaturated anilides to give zwitterionic intermediates which eliminate carboxylate and phenolate leaving groups

Jia, Jinli,Steinmetz, Mark G.,Shukla, Ruchi,Rathore, Rajendra

, p. 4621 - 4623 (2008)

α,β-Unsaturated anilides bearing allylic leaving groups undergo photochemical electrocyclic ring closure to produce zwitterionic intermediates which eliminate carboxylate and phenolate leaving groups.

Photochemical elimination of leaving groups from zwitterionic intermediates generated via electrocyclic ring closure of α,β-unsaturated anilides

Jia, Jinli,Sarker, Majher,Steinmetz, Mark G.,Shukla, Ruchi,Rathore, Rajendra

experimental part, p. 8867 - 8879 (2009/04/04)

(Chemical Equation Presented) Methacrylanilides, ArN(CH3) COC(CH2LG)=CH2, with allylic leaving groups (LG - = BocAla, PhCO2-, PhCH2CO 2-, PhO-) u

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