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176966-92-0

(4R,5S)-4-Allyl-5-(tert-butyl-diphenyl-silanyloxy)-2-oxo-piperidine-1-carboxylic acid tert-butyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 176966-92-0 Structure

  • Basic information

    1. Product Name: (4R,5S)-4-Allyl-5-(tert-butyl-diphenyl-silanyloxy)-2-oxo-piperidine-1-carboxylic acid tert-butyl ester
    2. Synonyms:
    3. CAS NO:176966-92-0
    4. Molecular Formula:
    5. Molecular Weight: 493.718
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 176966-92-0.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: (4R,5S)-4-Allyl-5-(tert-butyl-diphenyl-silanyloxy)-2-oxo-piperidine-1-carboxylic acid tert-butyl ester(CAS DataBase Reference)
    10. NIST Chemistry Reference: (4R,5S)-4-Allyl-5-(tert-butyl-diphenyl-silanyloxy)-2-oxo-piperidine-1-carboxylic acid tert-butyl ester(176966-92-0)
    11. EPA Substance Registry System: (4R,5S)-4-Allyl-5-(tert-butyl-diphenyl-silanyloxy)-2-oxo-piperidine-1-carboxylic acid tert-butyl ester(176966-92-0)

  • 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: 176966-92-0(Hazardous Substances Data)

176966-92-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 176966-92-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,7,6,9,6 and 6 respectively; the second part has 2 digits, 9 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 176966-92:
(8*1)+(7*7)+(6*6)+(5*9)+(4*6)+(3*6)+(2*9)+(1*2)=200
200 % 10 = 0
So 176966-92-0 is a valid CAS Registry Number.

176966-92-0Relevant articles and documents

Synthesis of homochiral piperidine derivatives from S-glutamic acid. Stereoselective 1,4-addition of organocuprates to a Δ3-piperidine-2-one. A paroxetine analogue

Herdeis,Kaschinski,Karla,Lotter

, p. 867 - 884 (2007/10/03)

Enantiomerically pure S-5-hydroxy-2-piperidinone 4, readily available from S-glutamic acid, serves as a key intermediate for the synthesis of 3,4-trans substituted piperidine derivatives. The substituents in the 4-position are introduced via 1,4-conjugate

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