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1144043-38-8

β-acetamido-β-(2-methoxyphenyl)-4-nitro-propiophenone is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1144043-38-8 Structure

  • Basic information

    1. Product Name: β-acetamido-β-(2-methoxyphenyl)-4-nitro-propiophenone
    2. Synonyms: β-acetamido-β-(2-methoxyphenyl)-4-nitro-propiophenone
    3. CAS NO:1144043-38-8
    4. Molecular Formula:
    5. Molecular Weight: 342.351
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1144043-38-8.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: β-acetamido-β-(2-methoxyphenyl)-4-nitro-propiophenone(CAS DataBase Reference)
    10. NIST Chemistry Reference: β-acetamido-β-(2-methoxyphenyl)-4-nitro-propiophenone(1144043-38-8)
    11. EPA Substance Registry System: β-acetamido-β-(2-methoxyphenyl)-4-nitro-propiophenone(1144043-38-8)

  • 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: 1144043-38-8(Hazardous Substances Data)

1144043-38-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1144043-38-8 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,1,4,4,0,4 and 3 respectively; the second part has 2 digits, 3 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 1144043-38:
(9*1)+(8*1)+(7*4)+(6*4)+(5*0)+(4*4)+(3*3)+(2*3)+(1*8)=108
108 % 10 = 8
So 1144043-38-8 is a valid CAS Registry Number.

1144043-38-8Downstream Products

1144043-38-8Relevant articles and documents

Cuso4 - 5h2o: A novel, green, reusable, and environmentally friendly catalyst for the one-pot, four-component synthesis of β-acetamido carbonyl compounds

Behbahani, Farahnaz K.,Doragi, Neda,Heravi, Majid M.

, p. 705 - 713 (2012)

Multicomponent reactions for the synthesis of β-acetamido carbonyl compounds have been gained considerable attention in organic synthesis. In this articles, aromatic aldehydes have been employed in a one-pot reaction with enolizable ketones, acetonitrile,

SnCl4/SiO2: An efficient heterogeneous alternative for one-pot synthesis of β-acetamidoketones

Mirjalili, Bi Bi Fatemeh,Hashemi, Mohammad M.,Sadeghi, Bahareh,Emtiazi, Hamideh

experimental part, p. 386 - 391 (2009/12/04)

Enolizable ketones have been reacted in a one-pot method with aromatic aldehydes, acetyl chloride and acetonitrile at room temperature in the presence of SnCl4/SiO2 to furnish the corresponding β-acetamidoketones in improved yields.

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