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(4E,3R)-2,2-bis(phenylsulfonyl)-3-acetoxy-5-phenyl-4-pentene is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 342909-04-0 Structure
  • Basic information

    1. Product Name: (4E,3R)-2,2-bis(phenylsulfonyl)-3-acetoxy-5-phenyl-4-pentene
    2. Synonyms: (4E,3R)-2,2-bis(phenylsulfonyl)-3-acetoxy-5-phenyl-4-pentene
    3. CAS NO:342909-04-0
    4. Molecular Formula:
    5. Molecular Weight: 484.594
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 342909-04-0.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: (4E,3R)-2,2-bis(phenylsulfonyl)-3-acetoxy-5-phenyl-4-pentene(CAS DataBase Reference)
    10. NIST Chemistry Reference: (4E,3R)-2,2-bis(phenylsulfonyl)-3-acetoxy-5-phenyl-4-pentene(342909-04-0)
    11. EPA Substance Registry System: (4E,3R)-2,2-bis(phenylsulfonyl)-3-acetoxy-5-phenyl-4-pentene(342909-04-0)
  • 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: 342909-04-0(Hazardous Substances Data)

342909-04-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 342909-04-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,4,2,9,0 and 9 respectively; the second part has 2 digits, 0 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 342909-04:
(8*3)+(7*4)+(6*2)+(5*9)+(4*0)+(3*9)+(2*0)+(1*4)=140
140 % 10 = 0
So 342909-04-0 is a valid CAS Registry Number.

342909-04-0Relevant articles and documents

Geminal dicarboxylates as carbonyl surrogates for asymmetric synthesis. Part II. Scope and applications

Trost,Chul Bom Lee

, p. 3687 - 3696 (2001)

An enantioselective synthesis of allylic esters has been achieved by a novel asymmetric alkylation of allylic gem-dicarboxylates. The catalyst derived from palladium(0) and R,R-1,2-di(2′-diphenylphosphinobenzamido)cyclohexene efficiently induced the alkyl

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