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CAS

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75100-48-0

3-Isopropyl-5-isopropylidene-[1,2,4]trithiolane is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 75100-48-0 Structure

  • Basic information

    1. Product Name: 3-Isopropyl-5-isopropylidene-[1,2,4]trithiolane
    2. Synonyms:
    3. CAS NO:75100-48-0
    4. Molecular Formula:
    5. Molecular Weight: 206.397
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 75100-48-0.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-Isopropyl-5-isopropylidene-[1,2,4]trithiolane(CAS DataBase Reference)
    10. NIST Chemistry Reference: 3-Isopropyl-5-isopropylidene-[1,2,4]trithiolane(75100-48-0)
    11. EPA Substance Registry System: 3-Isopropyl-5-isopropylidene-[1,2,4]trithiolane(75100-48-0)

  • 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: 75100-48-0(Hazardous Substances Data)

75100-48-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 75100-48-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,5,1,0 and 0 respectively; the second part has 2 digits, 4 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 75100-48:
(7*7)+(6*5)+(5*1)+(4*0)+(3*0)+(2*4)+(1*8)=100
100 % 10 = 0
So 75100-48-0 is a valid CAS Registry Number.

75100-48-0Downstream Products

75100-48-0Relevant articles and documents

DIMERES ET OLIGOMERES DES DITHIOACIDES ALIPHATIQUES OBTENUS PAR ACTION DE PEROXYDES OU DU RAYONNEMENT U. V.

Bonnans-Plaisance, Chantal,Mahjoub, Ahmed,Levesque, Guy

, p. 1941 - 1942 (2007/10/02)

Carbodithioic acids when heated with peroxydes lead to linear oligomers whose thermolysis gives rise to trithiolannes and tetrathiannes; U V irradiation leads to tetrathianne and cyclic oligomers.

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