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906371-08-2

tert-butyl (R)-2-(trimethylsilyl)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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  • 906371-08-2 Structure

  • Basic information

    1. Product Name: tert-butyl (R)-2-(trimethylsilyl)piperidine-1-carboxylate
    2. Synonyms:
    3. CAS NO:906371-08-2
    4. Molecular Formula:
    5. Molecular Weight: 257.448
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 906371-08-2.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: tert-butyl (R)-2-(trimethylsilyl)piperidine-1-carboxylate(CAS DataBase Reference)
    10. NIST Chemistry Reference: tert-butyl (R)-2-(trimethylsilyl)piperidine-1-carboxylate(906371-08-2)
    11. EPA Substance Registry System: tert-butyl (R)-2-(trimethylsilyl)piperidine-1-carboxylate(906371-08-2)

  • 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: 906371-08-2(Hazardous Substances Data)

906371-08-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 906371-08-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,0,6,3,7 and 1 respectively; the second part has 2 digits, 0 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 906371-08:
(8*9)+(7*0)+(6*6)+(5*3)+(4*7)+(3*1)+(2*0)+(1*8)=162
162 % 10 = 2
So 906371-08-2 is a valid CAS Registry Number.

906371-08-2Downstream Products

906371-08-2Relevant articles and documents

Dynamic kinetic and kinetic resolution of N-Boc-2-lithiopiperidine

Coldham, Iain,Patel, Jignesh J.,Raimbault, Sophie,Whittaker, David T. E.

, p. 4534 - 4536 (2008/09/16)

Asymmetric substitution of 2-lithiopiperidines can be achieved by dynamic resolution; the organolithium is formed as a racemic mixture by proton abstraction (or tin-lithium exchange) and is resolved in the presence of a chiral ligand. The Royal Society of

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