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74617-03-1

4-Chloro-3-phenyl-benzo[d]isothiazole is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 74617-03-1 Structure

  • Basic information

    1. Product Name: 4-Chloro-3-phenyl-benzo[d]isothiazole
    2. Synonyms:
    3. CAS NO:74617-03-1
    4. Molecular Formula:
    5. Molecular Weight: 245.732
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 74617-03-1.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: 4-Chloro-3-phenyl-benzo[d]isothiazole(CAS DataBase Reference)
    10. NIST Chemistry Reference: 4-Chloro-3-phenyl-benzo[d]isothiazole(74617-03-1)
    11. EPA Substance Registry System: 4-Chloro-3-phenyl-benzo[d]isothiazole(74617-03-1)

  • 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: 74617-03-1(Hazardous Substances Data)

74617-03-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 74617-03-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,4,6,1 and 7 respectively; the second part has 2 digits, 0 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 74617-03:
(7*7)+(6*4)+(5*6)+(4*1)+(3*7)+(2*0)+(1*3)=131
131 % 10 = 1
So 74617-03-1 is a valid CAS Registry Number.

74617-03-1Downstream Products

74617-03-1Relevant articles and documents

New Synthesis with Elemental Sulfur. - Preparation of 1,2-Benzisothiazoles and Some Secondary Reactions

Markert, Juergen,Hagen, Helmut

, p. 768 - 778 (2007/10/02)

The preparation of new 1,2-benzisothiazoles 2,3,5 and of thienoisothiazole 4 is described.The thioethers 8 have been obtained from 2 and 3 by ring opening with alcoholate and reaction with halomethyl compounds.On cyclisation, the thioethers 8 give the thionaphthenes 11.The ring systems of thionaphthenopyrimidines 10 and 12 have been prepared from 11.

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