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N-(2-Methyl-2-nitro-1-phenyl-propyl)-benzamide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 130564-43-1 Structure
  • Basic information

    1. Product Name: N-(2-Methyl-2-nitro-1-phenyl-propyl)-benzamide
    2. Synonyms: N-(2-Methyl-2-nitro-1-phenyl-propyl)-benzamide
    3. CAS NO:130564-43-1
    4. Molecular Formula:
    5. Molecular Weight: 298.342
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 130564-43-1.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-(2-Methyl-2-nitro-1-phenyl-propyl)-benzamide(CAS DataBase Reference)
    10. NIST Chemistry Reference: N-(2-Methyl-2-nitro-1-phenyl-propyl)-benzamide(130564-43-1)
    11. EPA Substance Registry System: N-(2-Methyl-2-nitro-1-phenyl-propyl)-benzamide(130564-43-1)
  • 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: 130564-43-1(Hazardous Substances Data)

130564-43-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 130564-43-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,0,5,6 and 4 respectively; the second part has 2 digits, 4 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 130564-43:
(8*1)+(7*3)+(6*0)+(5*5)+(4*6)+(3*4)+(2*4)+(1*3)=101
101 % 10 = 1
So 130564-43-1 is a valid CAS Registry Number.

130564-43-1Downstream Products

130564-43-1Relevant articles and documents

THE CHEMISTRY OF N-SUBSTITUTED BENZOTRIAZOLE. REACTIONS OF N-(α-AMINOALKYL)- AND N-(α-AMIDOALKYL)-BENZOTRIAZOLES WITH MONODEPROTONATED NITROALKANES

Karitzky, Alan R.,Saczewski, Franciszek

, p. 375 - 378 (2007/10/02)

N-(β-Nitroalkyl)amines 1a-i and N-(β-nitroalkyl)amides 1j-n are easily prepared by the C-amino(amido)alkylation of simple alkyl nitronate anions 3a-c with adducts 2a-i.The adducts themselves are readily available from one molecule each of an amine (or ami

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