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177213-44-4

(Z)-3-benzyloxy-1-(4-tolylsulfonyl)propene is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 177213-44-4 Structure

  • Basic information

    1. Product Name: (Z)-3-benzyloxy-1-(4-tolylsulfonyl)propene
    2. Synonyms: (Z)-3-benzyloxy-1-(4-tolylsulfonyl)propene
    3. CAS NO:177213-44-4
    4. Molecular Formula:
    5. Molecular Weight: 302.394
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 177213-44-4.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: (Z)-3-benzyloxy-1-(4-tolylsulfonyl)propene(CAS DataBase Reference)
    10. NIST Chemistry Reference: (Z)-3-benzyloxy-1-(4-tolylsulfonyl)propene(177213-44-4)
    11. EPA Substance Registry System: (Z)-3-benzyloxy-1-(4-tolylsulfonyl)propene(177213-44-4)

  • 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: 177213-44-4(Hazardous Substances Data)

177213-44-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 177213-44-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,7,7,2,1 and 3 respectively; the second part has 2 digits, 4 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 177213-44:
(8*1)+(7*7)+(6*7)+(5*2)+(4*1)+(3*3)+(2*4)+(1*4)=134
134 % 10 = 4
So 177213-44-4 is a valid CAS Registry Number.

177213-44-4Relevant articles and documents

(Alkoxyallyl)sulfones as enal β-anion equivalents. Synthesis of 5-substituted 2(5H)-furanones

Craig, Donald,Etheridge, Christopher J.,Smith, Alison M.

, p. 15267 - 15288 (1996)

2(5H)-Furanones 14 may be prepared in a four-step sequence starting from (alkoxyallyl)sulfone 10 and aldehydes.

Alkylation of oxiranyl anions

Mori, Yuji,Yaegashi, Keisuke,Iwase, Kazutaka,Yamamori, Yuki,Furukawa, Hiroshi

, p. 2605 - 2608 (2007/10/03)

Oxiranyllithium compounds generated from epoxy sulfones by deprotonation with n-butyllithium in THF at -100°C react with α-alkoxy alkyl triflates to give new substituted epoxides in high yields.

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