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929220-40-6

Acetamide, N-[(1S)-1-cyano-2,2-dimethylpropyl]-N-(phenylmethyl)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 929220-40-6 Structure

  • Basic information

    1. Product Name: Acetamide, N-[(1S)-1-cyano-2,2-dimethylpropyl]-N-(phenylmethyl)-
    2. Synonyms:
    3. CAS NO:929220-40-6
    4. Molecular Formula: C15H20N2O
    5. Molecular Weight: 244.337
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 929220-40-6.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: Acetamide, N-[(1S)-1-cyano-2,2-dimethylpropyl]-N-(phenylmethyl)-(CAS DataBase Reference)
    10. NIST Chemistry Reference: Acetamide, N-[(1S)-1-cyano-2,2-dimethylpropyl]-N-(phenylmethyl)-(929220-40-6)
    11. EPA Substance Registry System: Acetamide, N-[(1S)-1-cyano-2,2-dimethylpropyl]-N-(phenylmethyl)-(929220-40-6)

  • 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: 929220-40-6(Hazardous Substances Data)

929220-40-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 929220-40-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,2,9,2,2 and 0 respectively; the second part has 2 digits, 4 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 929220-40:
(8*9)+(7*2)+(6*9)+(5*2)+(4*2)+(3*0)+(2*4)+(1*0)=166
166 % 10 = 6
So 929220-40-6 is a valid CAS Registry Number.

929220-40-6Relevant articles and documents

Catalytic asymmetric acylcyanation of imines

Pan, Subhas Chandra,Zhou, Jian,List, Benjamin

, p. 612 - 614 (2007)

(Chemical Equation Presented) The less problematic acetyl cyanide can be used instead of toxic HCN for the highly enantioselective acyl-Strecker-type reaction. In the presence of an N-benzylimine and a catalytic amount of Jacobsen's catalyst 1, the desire

Catalytic asymmetric three-component acyl-strecker reaction

Pan, Subhas Chandra,List, Benjamin

, p. 1149 - 1151 (2007)

(Chemical Equation Presented) The first organocatalytic asymmetric three-component Strecker reaction, the urea-catalyzed acylcyanation of in situ generated imines, has been developed. Different α-amido nitriles are formed in excellent yields and enantiosl

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