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CAS

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856620-90-1

3-(phenylamino)butanamide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 856620-90-1 Structure

  • Basic information

    1. Product Name: 3-(phenylamino)butanamide
    2. Synonyms: 3-(phenylamino)butanamide
    3. CAS NO:856620-90-1
    4. Molecular Formula:
    5. Molecular Weight: 178.234
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 856620-90-1.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: 3-(phenylamino)butanamide(CAS DataBase Reference)
    10. NIST Chemistry Reference: 3-(phenylamino)butanamide(856620-90-1)
    11. EPA Substance Registry System: 3-(phenylamino)butanamide(856620-90-1)

  • 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: 856620-90-1(Hazardous Substances Data)

856620-90-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 856620-90-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,5,6,6,2 and 0 respectively; the second part has 2 digits, 9 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 856620-90:
(8*8)+(7*5)+(6*6)+(5*6)+(4*2)+(3*0)+(2*9)+(1*0)=191
191 % 10 = 1
So 856620-90-1 is a valid CAS Registry Number.

856620-90-1Downstream Products

856620-90-1Relevant articles and documents

Hofmann Rearrangement of Carboxamides Mediated by N-Bromoacetamide

Jevti?, Ivana I.,Do?en-Mi?ovi?, Ljiljana,Ivanovi?, Evica R.,Ivanovi?, Milovan D.

, p. 1550 - 1560 (2016)

An efficient, one-pot procedure for the Hofmann rearrangement of aromatic and aliphatic amides has been developed. Methyl and benzyl carbamates are produced with N-bromoacetamide in the presence of lithium hydroxide or lithium methoxide, in high yields. β-Phenylamino amides gave five-membered cyclic ureas stereospecifically. Side products of aryl or benzyl bromination were minimized. This procedure offers an easy access to various protected amines or diamines, which represent important synthetic precursors.

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