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101773-89-1

C19H24S2 is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 101773-89-1 Structure

  • Basic information

    1. Product Name: C19H24S2
    2. Synonyms:
    3. CAS NO:101773-89-1
    4. Molecular Formula:
    5. Molecular Weight: 316.532
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 101773-89-1.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: C19H24S2(CAS DataBase Reference)
    10. NIST Chemistry Reference: C19H24S2(101773-89-1)
    11. EPA Substance Registry System: C19H24S2(101773-89-1)

  • 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: 101773-89-1(Hazardous Substances Data)

101773-89-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 101773-89-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,1,7,7 and 3 respectively; the second part has 2 digits, 8 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 101773-89:
(8*1)+(7*0)+(6*1)+(5*7)+(4*7)+(3*3)+(2*8)+(1*9)=111
111 % 10 = 1
So 101773-89-1 is a valid CAS Registry Number.

101773-89-1Downstream Products

101773-89-1Relevant articles and documents

Reactions of Triplet Carbenes with Sulfides and Disulfides: Ylide vs. Radical Formation

Alberti, A.,Griller, D.,Nazran, A. S.,Pedulli, G. F.

, p. 3024 - 3028 (1986)

The reactions between triplet diphenylcarbene and fluorenylidene with a variety of sulfides and disulfides were investigated with use of electron paramagnetic resonance (EPR) spectroscopy, laser flash photolysis, and product studies.Diphenylcarbene reacted with these substrates by a radical-like displacement mechanism.Rate constants were ca. 1E6 M-1 s-1, and the resulting thio-substituted diphenylmethyl radicals were identified by their EPR and optical spectra.By contrast, the analogous reactions of fluorenylidene had rate constants of 1E8-1E9 M-1 s-1 and proceeded by an ylide mechanism.Product studies were consistent with these results but were not sufficient in themselves to reveal these mechanistic differences.

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