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1043572-02-6

C8H12Cl2S2 is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1043572-02-6 Structure

  • Basic information

    1. Product Name: C8H12Cl2S2
    2. Synonyms:
    3. CAS NO:1043572-02-6
    4. Molecular Formula:
    5. Molecular Weight: 243.221
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1043572-02-6.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: C8H12Cl2S2(CAS DataBase Reference)
    10. NIST Chemistry Reference: C8H12Cl2S2(1043572-02-6)
    11. EPA Substance Registry System: C8H12Cl2S2(1043572-02-6)

  • 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: 1043572-02-6(Hazardous Substances Data)

1043572-02-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1043572-02-6 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,4,3,5,7 and 2 respectively; the second part has 2 digits, 0 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 1043572-02:
(9*1)+(8*0)+(7*4)+(6*3)+(5*5)+(4*7)+(3*2)+(2*0)+(1*2)=116
116 % 10 = 6
So 1043572-02-6 is a valid CAS Registry Number.

1043572-02-6Downstream Products

1043572-02-6Relevant articles and documents

Generation and rearrangement of some spirocycloaliphatic thiosulfines and dithiiranes

Romanski, Jaroslaw,Reisenauer, Hans Peter,Petzold, Holm,Weigand, Wolfgang,Schreiner, Peter R.,Mloston, Grzegorz

, p. 2998 - 3003 (2008)

The flash-vacuum pyrolysis of selected dispirodicycloaliphatic 1,2,4-trithiolanes was studied by using matrix isolation techniques. The formation of thiosulfines and dithiiranes along with the corresponding thioketones was detected spectroscopically and confirmed by comparison with computed spectra. In the case of tetramethylcyclobutanone 1,2,4-trithiolane, the thermal formation of the dithiolactone was observed. Pyrolysis of the (dichloro)tetramethylcyclobutane derivative resulted only in the formation of a mixture of the thiosulfine and dithiirane. In this case, conversion into the corresponding dithiolactone could be achieved photochemically. The dispirodiadamantane derivative gave a mixture of the respective thiosulfine and dithiirane but no dithiolactone could be detected in the mixture. Wiley-VCH Verlag GmbH & Co. KGaA, 2008.

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