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methyl 3-(N-allylcarbamoyl)propanoate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 133055-19-3 Structure
  • Basic information

    1. Product Name: methyl 3-(N-allylcarbamoyl)propanoate
    2. Synonyms:
    3. CAS NO:133055-19-3
    4. Molecular Formula:
    5. Molecular Weight: 171.196
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 133055-19-3.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: methyl 3-(N-allylcarbamoyl)propanoate(CAS DataBase Reference)
    10. NIST Chemistry Reference: methyl 3-(N-allylcarbamoyl)propanoate(133055-19-3)
    11. EPA Substance Registry System: methyl 3-(N-allylcarbamoyl)propanoate(133055-19-3)
  • 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: 133055-19-3(Hazardous Substances Data)

133055-19-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 133055-19-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,3,0,5 and 5 respectively; the second part has 2 digits, 1 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 133055-19:
(8*1)+(7*3)+(6*3)+(5*0)+(4*5)+(3*5)+(2*1)+(1*9)=93
93 % 10 = 3
So 133055-19-3 is a valid CAS Registry Number.

133055-19-3Downstream Products

133055-19-3Relevant articles and documents

Selective ammonolysis and aminolysis of dimethyl succinate. Synthesis of optically active N-alkylsuccinimides

Puertas, Susana,Rebolledo, Francisca,Gotor, Vicente

, p. 1495 - 1502 (1995)

Candida antarctica lipase catalyzes the selective monoammonolysis and aminolysis of dimethyl succinate with ammonia and aliphatic amines, respectively, in dioxane as solvent. This enzyme shows a high enantioselectivity when racemic amines are used. Optically active amidoesters are also obtained in the reaction of dimethyl succinate with racemic α-methylalkylamines in hexane as solvent. In this medium, the enzyme catalyzes the formation of N-alkylsuccinimides or optically active N-alkyl-α-methylsuccinimides from dimethyl succinate or α-methylsuccinate and amines.

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