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(2S)-N-(tert-butoxycarbonyl)-2-[(4'-benzyloxy-1'-oxo)-E-but-2'-enyl]pyrrolidine is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 617689-99-3 Structure
  • Basic information

    1. Product Name: (2S)-N-(tert-butoxycarbonyl)-2-[(4'-benzyloxy-1'-oxo)-E-but-2'-enyl]pyrrolidine
    2. Synonyms: (2S)-N-(tert-butoxycarbonyl)-2-[(4'-benzyloxy-1'-oxo)-E-but-2'-enyl]pyrrolidine
    3. CAS NO:617689-99-3
    4. Molecular Formula:
    5. Molecular Weight: 345.439
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 617689-99-3.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: (2S)-N-(tert-butoxycarbonyl)-2-[(4'-benzyloxy-1'-oxo)-E-but-2'-enyl]pyrrolidine(CAS DataBase Reference)
    10. NIST Chemistry Reference: (2S)-N-(tert-butoxycarbonyl)-2-[(4'-benzyloxy-1'-oxo)-E-but-2'-enyl]pyrrolidine(617689-99-3)
    11. EPA Substance Registry System: (2S)-N-(tert-butoxycarbonyl)-2-[(4'-benzyloxy-1'-oxo)-E-but-2'-enyl]pyrrolidine(617689-99-3)
  • 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: 617689-99-3(Hazardous Substances Data)

617689-99-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 617689-99-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 6,1,7,6,8 and 9 respectively; the second part has 2 digits, 9 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 617689-99:
(8*6)+(7*1)+(6*7)+(5*6)+(4*8)+(3*9)+(2*9)+(1*9)=213
213 % 10 = 3
So 617689-99-3 is a valid CAS Registry Number.

617689-99-3Relevant articles and documents

Polyhydroxylated indolizidine alkaloids - An efficient synthesis of 1-deoxy-8,8a-di-epi-castanospermine

Koskinen, Ari M. P.,Kallatsa, Oili A.

, p. 6947 - 6954 (2003)

A new and efficient enantioselective total synthesis of the title deoxycastanospermine derivative has been developed, based on amino acid and β-ketophosphonate chemistry, as well as employment of internal asymmetric induction for the creation of the new chiral centers proved successful. With proper choice of reaction conditions, the approach can also be applied in selective preparation of several isomers of deoxycastanospermine. The length (9 steps) and overall yield of the title compound trihydroxyindolidine 1, 7.3%, compares well with the literature syntheses of similar compounds.

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