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CAS

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65500-83-6

Hexanamide, 6-[(1-oxo-2-propenyl)amino]-N-phenyl- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 65500-83-6 Structure

  • Basic information

    1. Product Name: Hexanamide, 6-[(1-oxo-2-propenyl)amino]-N-phenyl-
    2. Synonyms:
    3. CAS NO:65500-83-6
    4. Molecular Formula: C15H20N2O2
    5. Molecular Weight: 260.336
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 65500-83-6.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: Hexanamide, 6-[(1-oxo-2-propenyl)amino]-N-phenyl-(CAS DataBase Reference)
    10. NIST Chemistry Reference: Hexanamide, 6-[(1-oxo-2-propenyl)amino]-N-phenyl-(65500-83-6)
    11. EPA Substance Registry System: Hexanamide, 6-[(1-oxo-2-propenyl)amino]-N-phenyl-(65500-83-6)

  • 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: 65500-83-6(Hazardous Substances Data)

65500-83-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 65500-83-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,5,5,0 and 0 respectively; the second part has 2 digits, 8 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 65500-83:
(7*6)+(6*5)+(5*5)+(4*0)+(3*0)+(2*8)+(1*3)=116
116 % 10 = 6
So 65500-83-6 is a valid CAS Registry Number.

65500-83-6Downstream Products

65500-83-6Relevant articles and documents

Design and synthesis of non-hydroxamate histone deacetylase inhibitors: Identification of a selective histone acetylating agent

Suzuki, Takayoshi,Matsuura, Azusa,Kouketsu, Akiyasu,Hisakawa, Shinya,Nakagawa, Hidehiko,Miyata, Naoki

, p. 4332 - 4342 (2007/10/03)

A series of suberoylanilide hydroxamic acid (SAHA)-based non-hydroxamates was designed, synthesized, and evaluated for their histone deacetylase (HDAC) inhibitory activity. Among these, methyl sulfoxide 15 inhibited HDACs in enzyme assays and caused hyperacetylation of histone H4 while not inducing the accumulation of acetylated α-tubulin in HCT116 cells.

Synthese et proprietes de monomeres acryliques porteurs d'un groupement fonctionnel acylant. Preparation d'un nouveau copolymere acylant pour l'immobilisation des biomolecules

Joyeau, Roger,Brown, Eric

, p. 391 - 394 (2007/10/02)

Carboxylic acids bearing an ω-acrylamido group were reacted with mercaptothiazoline in the presence of DCC to give the corresponding N-acyl thiazolidin-2-thiones (3 - 5) in good yields.On treatment with benzylamine, piperidine or aniline, these acyl deriv

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