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CAS

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1160937-42-7

N-[12-azido-1-benzyl-1-(N,N-dimethylcarbamoyl)dodecyl]benzamide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1160937-42-7 Structure

  • Basic information

    1. Product Name: N-[12-azido-1-benzyl-1-(N,N-dimethylcarbamoyl)dodecyl]benzamide
    2. Synonyms: N-[12-azido-1-benzyl-1-(N,N-dimethylcarbamoyl)dodecyl]benzamide
    3. CAS NO:1160937-42-7
    4. Molecular Formula:
    5. Molecular Weight: 491.677
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1160937-42-7.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-[12-azido-1-benzyl-1-(N,N-dimethylcarbamoyl)dodecyl]benzamide(CAS DataBase Reference)
    10. NIST Chemistry Reference: N-[12-azido-1-benzyl-1-(N,N-dimethylcarbamoyl)dodecyl]benzamide(1160937-42-7)
    11. EPA Substance Registry System: N-[12-azido-1-benzyl-1-(N,N-dimethylcarbamoyl)dodecyl]benzamide(1160937-42-7)

  • 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: 1160937-42-7(Hazardous Substances Data)

1160937-42-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1160937-42-7 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,1,6,0,9,3 and 7 respectively; the second part has 2 digits, 4 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 1160937-42:
(9*1)+(8*1)+(7*6)+(6*0)+(5*9)+(4*3)+(3*7)+(2*4)+(1*2)=147
147 % 10 = 7
So 1160937-42-7 is a valid CAS Registry Number.

1160937-42-7Relevant articles and documents

Synthesis of macrocyclic lactams from 2-(ω-amino-alkyl)-2-benzoylamino-3-phenyl-N,N-dimethylpropan-amides via direct amide cyclization

Fritschi, Stephan P.,Linden, Anthony,Heimgartner, Heinz

, p. 985 - 1005 (2009)

The alkylation of 4-benzyl-2-phenyl-1,3-oxazol-5(4H)-one (11) with (ω-azidoalkyl iodides (12) by deprotonation with LDA in THF/HMPT at -78 °C yielded mixtures of the 4,4-disubstituted l,3-oxazol-5(4H)-ones (13) and the O-alkylated 1,3-oxazoles (14) in 65-

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