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1268357-03-4

2,3-diallyl-4-(phenylthio)-3-sulfolene is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1268357-03-4 Structure

  • Basic information

    1. Product Name: 2,3-diallyl-4-(phenylthio)-3-sulfolene
    2. Synonyms: 2,3-diallyl-4-(phenylthio)-3-sulfolene
    3. CAS NO:1268357-03-4
    4. Molecular Formula:
    5. Molecular Weight: 306.45
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1268357-03-4.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: 2,3-diallyl-4-(phenylthio)-3-sulfolene(CAS DataBase Reference)
    10. NIST Chemistry Reference: 2,3-diallyl-4-(phenylthio)-3-sulfolene(1268357-03-4)
    11. EPA Substance Registry System: 2,3-diallyl-4-(phenylthio)-3-sulfolene(1268357-03-4)

  • 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: 1268357-03-4(Hazardous Substances Data)

1268357-03-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1268357-03-4 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,6,8,3,5 and 7 respectively; the second part has 2 digits, 0 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 1268357-03:
(9*1)+(8*2)+(7*6)+(6*8)+(5*3)+(4*5)+(3*7)+(2*0)+(1*3)=174
174 % 10 = 4
So 1268357-03-4 is a valid CAS Registry Number.

1268357-03-4Upstream product

1268357-03-4Relevant articles and documents

Synthesis and applications of sulfur-substituted cis-hexahydro-2- quinolinones

Chou, Shang-Shing P.,Cai, Yi-Lin

, p. 1183 - 1186 (2011)

An efficient synthesis of sulfur-substituted cis-hexahydro-2-quinolinones has been achieved by an aza-Diels-Alder reaction of p-toluenesulfonyl isocyanate with a diene precursor derived from a bicyclic 3-sulfolene via ring-closing metathesis. S

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