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1514644-79-1

benzyl (2S)-2-[(1R)-1,2-dihydroxyethyl]piperidine-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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  • 1514644-79-1 Structure

  • Basic information

    1. Product Name: benzyl (2S)-2-[(1R)-1,2-dihydroxyethyl]piperidine-1-carboxylate
    2. Synonyms: benzyl (2S)-2-[(1R)-1,2-dihydroxyethyl]piperidine-1-carboxylate
    3. CAS NO:1514644-79-1
    4. Molecular Formula:
    5. Molecular Weight: 279.336
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1514644-79-1.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: benzyl (2S)-2-[(1R)-1,2-dihydroxyethyl]piperidine-1-carboxylate(CAS DataBase Reference)
    10. NIST Chemistry Reference: benzyl (2S)-2-[(1R)-1,2-dihydroxyethyl]piperidine-1-carboxylate(1514644-79-1)
    11. EPA Substance Registry System: benzyl (2S)-2-[(1R)-1,2-dihydroxyethyl]piperidine-1-carboxylate(1514644-79-1)

  • 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: 1514644-79-1(Hazardous Substances Data)

1514644-79-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1514644-79-1 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,5,1,4,6,4 and 4 respectively; the second part has 2 digits, 7 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 1514644-79:
(9*1)+(8*5)+(7*1)+(6*4)+(5*6)+(4*4)+(3*4)+(2*7)+(1*9)=161
161 % 10 = 1
So 1514644-79-1 is a valid CAS Registry Number.

1514644-79-1Relevant articles and documents

Synthetic studies of alkaloids containing pyrrolidine and piperidine structural motifs

Bhat, Chinmay

, p. 192 - 196 (2015/04/27)

Avenues to asymmetric alkaloids! Various 2-substituted pyrrolidine and piperidine chiral bioactive natural products were synthesized using a 'chiral pool' method. l-proline and l-pipecolinic acids with one chiral center served as the best precursors for the synthesis of these alkaloids. Overall, 14 total synthetic and 11 formal synthetic approaches were developed.

A concise diastereoselective approach to (+)-dexoxadrol, (-)-epi-dexoxadrol, (-)-conhydrine and (+)-lentiginosine from (-)-pipecolinic acid

Bhat, Chinmay,Tilve, Santosh G.

, p. 10876 - 10883 (2014/01/06)

A new diastereoselective pathway for the total synthesis of (+)-dexoxadrol, first asymmetric synthesis of (-)-epi-dexoxadrol and formal synthesis of conhydrine and (+)-lentiginosine is presented using commercially available (-)-pipecolinic acid. The key reactions utilized are Sharpless asymmetric dihydroxylation and Wittig reaction. The paper further describes the study of effect of protecting groups on dihydroxylation of a terminal olefin in piperidine ring system.

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