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1227635-49-5

α-benzyl-N-benzyloxycarbonylpiperidine is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1227635-49-5 Structure

  • Basic information

    1. Product Name: α-benzyl-N-benzyloxycarbonylpiperidine
    2. Synonyms: α-benzyl-N-benzyloxycarbonylpiperidine
    3. CAS NO:1227635-49-5
    4. Molecular Formula:
    5. Molecular Weight: 309.408
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1227635-49-5.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: α-benzyl-N-benzyloxycarbonylpiperidine(CAS DataBase Reference)
    10. NIST Chemistry Reference: α-benzyl-N-benzyloxycarbonylpiperidine(1227635-49-5)
    11. EPA Substance Registry System: α-benzyl-N-benzyloxycarbonylpiperidine(1227635-49-5)

  • 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: 1227635-49-5(Hazardous Substances Data)

1227635-49-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1227635-49-5 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,2,7,6,3 and 5 respectively; the second part has 2 digits, 4 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 1227635-49:
(9*1)+(8*2)+(7*2)+(6*7)+(5*6)+(4*3)+(3*5)+(2*4)+(1*9)=155
155 % 10 = 5
So 1227635-49-5 is a valid CAS Registry Number.

1227635-49-5Relevant articles and documents

Catalytic kinetic resolution of cyclic secondary amines

Binanzer, Michael,Hsieh, Sheng-Ying,Bode, Jeffrey W.

supporting information; experimental part, p. 19698 - 19701 (2012/01/13)

The catalytic resolution of racemic cyclic amines has been achieved by an enantioselective amidation reaction featuring an achiral N-heterocyclic carbene catalyst and a new chiral hydroxamic acid cocatalyst working in concert. The reactions proceed at room temperature, do not generate nonvolatile byproducts, and provide enantioenriched amines by aqueous extraction.

Electrochemical deallylation of α-allyl cyclic amines and synthesis of optically active quaternary cyclic amino acids

Kirira, Peter G.,Kuriyama, Masami,Onomura, Osamu

experimental part, p. 3970 - 3982 (2010/07/04)

Electrochemical oxidation of α-allylated and α-betizylated N-acylated cyclic amines by using a graphite anode easily affords the corresponding α-methoxylated products with up to 76% yield. Ease of oxidation was affected by the type of electrode, the size

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