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Acetamide, N-[3-nitro-2-oxo-1-(phenylmethyl)propyl]-, (S)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 139168-60-8 Structure
  • Basic information

    1. Product Name: Acetamide, N-[3-nitro-2-oxo-1-(phenylmethyl)propyl]-, (S)-
    2. Synonyms:
    3. CAS NO:139168-60-8
    4. Molecular Formula: C12H14N2O4
    5. Molecular Weight: 250.254
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 139168-60-8.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-[3-nitro-2-oxo-1-(phenylmethyl)propyl]-, (S)-(CAS DataBase Reference)
    10. NIST Chemistry Reference: Acetamide, N-[3-nitro-2-oxo-1-(phenylmethyl)propyl]-, (S)-(139168-60-8)
    11. EPA Substance Registry System: Acetamide, N-[3-nitro-2-oxo-1-(phenylmethyl)propyl]-, (S)-(139168-60-8)
  • 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: 139168-60-8(Hazardous Substances Data)

139168-60-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 139168-60-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,9,1,6 and 8 respectively; the second part has 2 digits, 6 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 139168-60:
(8*1)+(7*3)+(6*9)+(5*1)+(4*6)+(3*8)+(2*6)+(1*0)=148
148 % 10 = 8
So 139168-60-8 is a valid CAS Registry Number.

139168-60-8Downstream Products

139168-60-8Relevant articles and documents

Silica-Gel-Catalysed Knoevenagel Condensation of Peptidyl Cyanomethyl Ketones with Aromatic Aldehydes and Ketones. A Novel Michael Acceptor Functionality for C-Modified Peptides: The Benzylidene and Alkylidene Cyanomethyl Ketone Function

Brillon, Denis,Sauve, Gilles

, p. 1838 - 1842 (1992)

Simple preparation of cyanomethyl ketone derivatives 5a-5b of N-acetylphenylalanine and N-acetylleucylphenylalanine is accomplished by condensation of the corresponding activated carboxylic acids 3a-3b and the carbanion of tert-butyl cyanoacetate to give

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