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CAS

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387381-73-9

N-[1,2,2-tris-(4-chloro-phenylsulfanyl)-vinyl]-benzamide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 387381-73-9 Structure

  • Basic information

    1. Product Name: N-[1,2,2-tris-(4-chloro-phenylsulfanyl)-vinyl]-benzamide
    2. Synonyms: N-[1,2,2-tris-(4-chloro-phenylsulfanyl)-vinyl]-benzamide
    3. CAS NO:387381-73-9
    4. Molecular Formula:
    5. Molecular Weight: 575.003
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 387381-73-9.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-[1,2,2-tris-(4-chloro-phenylsulfanyl)-vinyl]-benzamide(CAS DataBase Reference)
    10. NIST Chemistry Reference: N-[1,2,2-tris-(4-chloro-phenylsulfanyl)-vinyl]-benzamide(387381-73-9)
    11. EPA Substance Registry System: N-[1,2,2-tris-(4-chloro-phenylsulfanyl)-vinyl]-benzamide(387381-73-9)

  • 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: 387381-73-9(Hazardous Substances Data)

387381-73-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 387381-73-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,8,7,3,8 and 1 respectively; the second part has 2 digits, 7 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 387381-73:
(8*3)+(7*8)+(6*7)+(5*3)+(4*8)+(3*1)+(2*7)+(1*3)=189
189 % 10 = 9
So 387381-73-9 is a valid CAS Registry Number.

387381-73-9Relevant articles and documents

Conversion of N-(1-arylsulfonyl-2,2-dichloroethenyl)carboxamides into derivatives of 4,5-dimercaptooxazole

Babii,Zyabrev,Drach

, p. 1149 - 1152 (2007/10/03)

In reaction of excess thiols with α-arylsulfonyl-substituted enamides containing two chlorine atoms in β-position to the amide moiety the chlorine atoms and the arylsulfonyl group attached to the C = C bond are replaced by alkylthio or arylthio groups. The sulfur-containing enamides obtained undergo cyclization when treated with phosphorus pentachloride or thionyl chloride to furnish 4,5-dimercaptooxazoles used for preparation of the corresponding disulfonyl derivatives. The latter were also obtained by treating in succession the N-(1-arylsulfonyl-2,2-dichloroethenyl)carboxamides with sodium hydrosulfide, then with alkyl halides, and hydrogen peroxide in acetic acid.

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