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2-Piperidinecarboxamide,2-methyl-,(R)-(9CI) is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 132259-55-3 Structure
  • Basic information

    1. Product Name: 2-Piperidinecarboxamide,2-methyl-,(R)-(9CI)
    2. Synonyms: 2-Piperidinecarboxamide,2-methyl-,(R)-(9CI)
    3. CAS NO:132259-55-3
    4. Molecular Formula: C7H14N2O
    5. Molecular Weight: 142.2
    6. EINECS: N/A
    7. Product Categories: AMIDE
    8. Mol File: 132259-55-3.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: 2-Piperidinecarboxamide,2-methyl-,(R)-(9CI)(CAS DataBase Reference)
    10. NIST Chemistry Reference: 2-Piperidinecarboxamide,2-methyl-,(R)-(9CI)(132259-55-3)
    11. EPA Substance Registry System: 2-Piperidinecarboxamide,2-methyl-,(R)-(9CI)(132259-55-3)
  • 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: 132259-55-3(Hazardous Substances Data)

132259-55-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 132259-55-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,2,2,5 and 9 respectively; the second part has 2 digits, 5 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 132259-55:
(8*1)+(7*3)+(6*2)+(5*2)+(4*5)+(3*9)+(2*5)+(1*5)=113
113 % 10 = 3
So 132259-55-3 is a valid CAS Registry Number.

132259-55-3Relevant articles and documents

Preparation and Use of Chloromethyl (-)-Menthyl Ether in the Synthesis of Optically Pure α-Branched α-Amino Nitriles

Shatzmiller, Shimon,Dolithzky, Ben-Zion,Bahar, Eliezer

, p. 375 - 379 (2007/10/02)

The synthesis of optically pure chloromethyl (-)-menthyl ether (2b) and its use in the synthesis of di-(-)-menthyl acetal (-)-menthyl (+)-menthyl acetals are described.The diastereomeric mixed acetals 7a,b and 8a,b are easily obtainable from the nitrones 5 and 6, KCN and 2b.The mixture of diastereomers are separated into the pure components 7a, 7b and 8a, 8b by simple silica gel column chromatography.Hydrolysis of these products (H2O2/Na2CO3, ultrasound) followed by N-O cleavage affords the heterocyclic α-methyl-α-amino amides 11a, 11b and 12a, 12b.These are subsequently hydrolyzed to give the corresponding α-methyl-α-amino acids with S and R configuration, respectively.

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