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CAS

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228417-08-1

(+)-(αR,2S,3S)-2-(α-hydroxybenzyl)-2-(p-tolylsulfonyl)-3-vinyloxirane is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 228417-08-1 Structure

  • Basic information

    1. Product Name: (+)-(αR,2S,3S)-2-(α-hydroxybenzyl)-2-(p-tolylsulfonyl)-3-vinyloxirane
    2. Synonyms: (+)-(αR,2S,3S)-2-(α-hydroxybenzyl)-2-(p-tolylsulfonyl)-3-vinyloxirane
    3. CAS NO:228417-08-1
    4. Molecular Formula:
    5. Molecular Weight: 330.405
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 228417-08-1.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: (+)-(αR,2S,3S)-2-(α-hydroxybenzyl)-2-(p-tolylsulfonyl)-3-vinyloxirane(CAS DataBase Reference)
    10. NIST Chemistry Reference: (+)-(αR,2S,3S)-2-(α-hydroxybenzyl)-2-(p-tolylsulfonyl)-3-vinyloxirane(228417-08-1)
    11. EPA Substance Registry System: (+)-(αR,2S,3S)-2-(α-hydroxybenzyl)-2-(p-tolylsulfonyl)-3-vinyloxirane(228417-08-1)

  • 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: 228417-08-1(Hazardous Substances Data)

228417-08-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 228417-08-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,2,8,4,1 and 7 respectively; the second part has 2 digits, 0 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 228417-08:
(8*2)+(7*2)+(6*8)+(5*4)+(4*1)+(3*7)+(2*0)+(1*8)=131
131 % 10 = 1
So 228417-08-1 is a valid CAS Registry Number.

228417-08-1Relevant articles and documents

Highly stereoselective metal-catalyzed epoxidation of hydroxy vinyl sulfones

Fernandez De La Pradilla, Roberto,Mendez, Paloma,Priego, Julian,Viso, Alma

, p. 1247 - 1249 (2007/10/03)

Acyclic α-hydroxyalkyl α,β-unsaturated sulfoxides undergo oxidation at sulfur followed by a highly regio- and stereoselective epoxidation at the electron deficient alkene by treatment with ButOOH-VO(acac)2; this methodology allows fo

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