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93646-37-8

3-Butenamide, N-(2-chlorophenyl)-N,3-dimethyl- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 93646-37-8 Structure

  • Basic information

    1. Product Name: 3-Butenamide, N-(2-chlorophenyl)-N,3-dimethyl-
    2. Synonyms:
    3. CAS NO:93646-37-8
    4. Molecular Formula: C12H14ClNO
    5. Molecular Weight: 223.702
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 93646-37-8.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: 3-Butenamide, N-(2-chlorophenyl)-N,3-dimethyl-(CAS DataBase Reference)
    10. NIST Chemistry Reference: 3-Butenamide, N-(2-chlorophenyl)-N,3-dimethyl-(93646-37-8)
    11. EPA Substance Registry System: 3-Butenamide, N-(2-chlorophenyl)-N,3-dimethyl-(93646-37-8)

  • 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: 93646-37-8(Hazardous Substances Data)

93646-37-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 93646-37-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,3,6,4 and 6 respectively; the second part has 2 digits, 3 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 93646-37:
(7*9)+(6*3)+(5*6)+(4*4)+(3*6)+(2*3)+(1*7)=158
158 % 10 = 8
So 93646-37-8 is a valid CAS Registry Number.

93646-37-8Downstream Products

93646-37-8Relevant articles and documents

Photoinduced Cyclizations of Mono- and Dianions of N-Acyl-o-chloroanilines and N-Acyl-o-chlorobenzylamines as General Methods for the Synthesis of Oxindoles and 1,4-Dihydro-3(2H)-isoquinolinones

Goehring, R. Richard,Sachdeva, Yesh P.,Pisipati, Jyothi S.,Sleevi, Mark C.,Wolfe, James F.

, p. 435 - 443 (2007/10/02)

Formation of the monoanions of a series of N-acyl-N-alkyl-o-chloroanilines by means of LDA in THF followed by irradiation with near-UV light affords 1,3-dialkyloxindoles in good yields.Similar photoinduced cyclizations of dianions derived from N-acyl-o-chloroanilines leads to 3-alkyloxindoles.Photocyclizations of mono- and dianion prepared from α,β-unsaturated o-haloanilides proceed to form 3-alkylideneoxindoles.Carbanions derived from N-acyl-o-chlorobenzylamines also undergo photoassisted ring closure to afford 1,4-dihydro-3(2H)-isoquinolinones.The influence of near-UV light and the effect of inhibitors implicate a radical-chain mechanism as the major reaction pathway in this convenient new method for oxindole and isoquinolinone synthesis.

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