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1004993-43-4

tert-butyl (2S)-2-[(phenylselenonyl)methyl]pyrrolidine-1-carboxylate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1004993-43-4 Structure

  • Basic information

    1. Product Name: tert-butyl (2S)-2-[(phenylselenonyl)methyl]pyrrolidine-1-carboxylate
    2. Synonyms:
    3. CAS NO:1004993-43-4
    4. Molecular Formula:
    5. Molecular Weight: 372.323
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1004993-43-4.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: tert-butyl (2S)-2-[(phenylselenonyl)methyl]pyrrolidine-1-carboxylate(CAS DataBase Reference)
    10. NIST Chemistry Reference: tert-butyl (2S)-2-[(phenylselenonyl)methyl]pyrrolidine-1-carboxylate(1004993-43-4)
    11. EPA Substance Registry System: tert-butyl (2S)-2-[(phenylselenonyl)methyl]pyrrolidine-1-carboxylate(1004993-43-4)

  • 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: 1004993-43-4(Hazardous Substances Data)

1004993-43-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1004993-43-4 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,0,4,9,9 and 3 respectively; the second part has 2 digits, 4 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 1004993-43:
(9*1)+(8*0)+(7*0)+(6*4)+(5*9)+(4*9)+(3*3)+(2*4)+(1*3)=134
134 % 10 = 4
So 1004993-43-4 is a valid CAS Registry Number.

1004993-43-4Upstream product

1004993-43-4Relevant articles and documents

Selenium promoted synthesis of enantiopure pyrrolidines starting from chiral aminoalcohols

Tiecco, Marcello,Testaferri, Lorenzo,Bagnoli, Luana,Scarponi, Catalina,Temperini, Andrea,Marini, Francesca,Santi, Claudio

, p. 2758 - 2767 (2008/03/28)

Starting from commercially available enantiomerically pure aminoalcohols and using simple conversions promoted by organoselenium reagents, several enantiomerically pure substituted pyrrolidines were prepared. After double protections (R)- or (S)-2-phenylg

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