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908344-12-7

(E)-benzyl(4-chlorostyryl)sulfane is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 908344-12-7 Structure

  • Basic information

    1. Product Name: (E)-benzyl(4-chlorostyryl)sulfane
    2. Synonyms: (E)-benzyl(4-chlorostyryl)sulfane
    3. CAS NO:908344-12-7
    4. Molecular Formula:
    5. Molecular Weight: 260.787
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 908344-12-7.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: (E)-benzyl(4-chlorostyryl)sulfane(CAS DataBase Reference)
    10. NIST Chemistry Reference: (E)-benzyl(4-chlorostyryl)sulfane(908344-12-7)
    11. EPA Substance Registry System: (E)-benzyl(4-chlorostyryl)sulfane(908344-12-7)

  • 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: 908344-12-7(Hazardous Substances Data)

908344-12-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 908344-12-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,0,8,3,4 and 4 respectively; the second part has 2 digits, 1 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 908344-12:
(8*9)+(7*0)+(6*8)+(5*3)+(4*4)+(3*4)+(2*1)+(1*2)=167
167 % 10 = 7
So 908344-12-7 is a valid CAS Registry Number.

908344-12-7Downstream Products

908344-12-7Relevant articles and documents

One-pot synthesis of alkyl styryl sulfides free from transition metal/ligand catalyst and thiols

Heredia, Adrian A.,Penenory, Alicia B.

, p. 991 - 997 (2013)

A new protocol for the one-pot synthesis of styryl alkyl sulfides was developed. This methodology involves the in situ generation of thiolate anions by nucleophilic substitution between potassium thioacetate and alkyl halides followed by fragmentation. Further reactions of these thiolate anions with substituted (E,Z)-β-styryl halides gave the corresponding sulfides with retention of stereochemistry in good to excellent yields. This procedure does not require a metal catalyst, it proceeds under mild conditions and in short times, and it is free from malodorous and air-sensitive alkyl thiols. Copyright

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