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144463-73-0

Benzoic acid, 2-(phenylthio)-, 2-propenyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 144463-73-0 Structure

  • Basic information

    1. Product Name: Benzoic acid, 2-(phenylthio)-, 2-propenyl ester
    2. Synonyms:
    3. CAS NO:144463-73-0
    4. Molecular Formula: C16H14O2S
    5. Molecular Weight: 270.352
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 144463-73-0.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: Benzoic acid, 2-(phenylthio)-, 2-propenyl ester(CAS DataBase Reference)
    10. NIST Chemistry Reference: Benzoic acid, 2-(phenylthio)-, 2-propenyl ester(144463-73-0)
    11. EPA Substance Registry System: Benzoic acid, 2-(phenylthio)-, 2-propenyl ester(144463-73-0)

  • 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: 144463-73-0(Hazardous Substances Data)

144463-73-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 144463-73-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,4,4,6 and 3 respectively; the second part has 2 digits, 7 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 144463-73:
(8*1)+(7*4)+(6*4)+(5*4)+(4*6)+(3*3)+(2*7)+(1*3)=130
130 % 10 = 0
So 144463-73-0 is a valid CAS Registry Number.

144463-73-0Downstream Products

144463-73-0Relevant articles and documents

Gas phase generation and cyclisation reactions of some o-substituted phenyl radicals

Cadogan,Hutchison,McNab

, p. 7747 - 7762 (2007/10/02)

Flash vacuum pyrolysis of the allyl esters 2 (X=O, S, CH2, CO) at 900°C (10-2 Torr) gives dibenzofurans, dibenzothiophenes, fluorenes, and fluorenones respectively as the major products. The mechanism involves the phenyl radical intermediates 1 which equilibrate by intramolecular hydrogen transfer via six-membered transition states, prior to cyclisation.

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