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132735-14-9

2-(4-chlorophenyl)-3,6-dihydro-2H-1,2-thiazine is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 132735-14-9 Structure

  • Basic information

    1. Product Name: 2-(4-chlorophenyl)-3,6-dihydro-2H-1,2-thiazine
    2. Synonyms: 2-(4-chlorophenyl)-3,6-dihydro-2H-1,2-thiazine
    3. CAS NO:132735-14-9
    4. Molecular Formula:
    5. Molecular Weight: 211.715
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 132735-14-9.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: 2-(4-chlorophenyl)-3,6-dihydro-2H-1,2-thiazine(CAS DataBase Reference)
    10. NIST Chemistry Reference: 2-(4-chlorophenyl)-3,6-dihydro-2H-1,2-thiazine(132735-14-9)
    11. EPA Substance Registry System: 2-(4-chlorophenyl)-3,6-dihydro-2H-1,2-thiazine(132735-14-9)

  • 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: 132735-14-9(Hazardous Substances Data)

132735-14-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 132735-14-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,2,7,3 and 5 respectively; the second part has 2 digits, 1 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 132735-14:
(8*1)+(7*3)+(6*2)+(5*7)+(4*3)+(3*5)+(2*1)+(1*4)=109
109 % 10 = 9
So 132735-14-9 is a valid CAS Registry Number.

132735-14-9Downstream Products

132735-14-9Relevant articles and documents

Generation of Thionitrosoarenes (ArN=S) from N-(Arylaminothio)phthalimides and in situ Trapping with Alkenes and Conjugated Dienes

Bryce, Martin R.,Taylor, Paul C.

, p. 3225 - 3235 (1990)

A series of N-(arylaminothio)phthalimide derivatives (7a-h) has been prepared by reaction of phthalimidesulphenyl chloride with the trimethylsilyl derivative of the appropriate arylamine.On treatment with triethylamine at room temperature, compounds (7) fragment to yield transient thionitroso species (8).Derivatives (8a-h) have been trapped in good yield as their Diels-Alder adducts with the following conjugated dienes: butadiene, 2.3-dimethylbutadiene, 1.4-diphenylbutadiene, (E,E)- and (E,Z)-hexa-2,4-diene, 1,1'-bicyclopentenyl (25) and 1,1'-bicyclohexenyl (26).The stereochemistry of the diene is retained in the adducts (19)-(24).Thionitrosoarene derivatives (8) also afford sulphenamide derivatives, e.g. (11) and (12)-(16), by ene addition to dimethylbutadiene, isobutene, and α-methylstyrene.N-Aryliminosulphur dichlorides (34) react with 2,3-dimethylbutadiene to yield 1,2-thiazine and sulphenamide products, probably by way of thionitrosoarene intermediates.

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