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benzyl (1S)-1-(2-{[tert-butyl(dimethyl)silyl]oxy}ethyl)-2-oxo-undec-3-ynylcarbamate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 686722-16-7 Structure
  • Basic information

    1. Product Name: benzyl (1S)-1-(2-{[tert-butyl(dimethyl)silyl]oxy}ethyl)-2-oxo-undec-3-ynylcarbamate
    2. Synonyms: benzyl (1S)-1-(2-{[tert-butyl(dimethyl)silyl]oxy}ethyl)-2-oxo-undec-3-ynylcarbamate
    3. CAS NO:686722-16-7
    4. Molecular Formula:
    5. Molecular Weight: 473.728
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 686722-16-7.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 (1S)-1-(2-{[tert-butyl(dimethyl)silyl]oxy}ethyl)-2-oxo-undec-3-ynylcarbamate(CAS DataBase Reference)
    10. NIST Chemistry Reference: benzyl (1S)-1-(2-{[tert-butyl(dimethyl)silyl]oxy}ethyl)-2-oxo-undec-3-ynylcarbamate(686722-16-7)
    11. EPA Substance Registry System: benzyl (1S)-1-(2-{[tert-butyl(dimethyl)silyl]oxy}ethyl)-2-oxo-undec-3-ynylcarbamate(686722-16-7)
  • 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: 686722-16-7(Hazardous Substances Data)

686722-16-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 686722-16-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 6,8,6,7,2 and 2 respectively; the second part has 2 digits, 1 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 686722-16:
(8*6)+(7*8)+(6*6)+(5*7)+(4*2)+(3*2)+(2*1)+(1*6)=197
197 % 10 = 7
So 686722-16-7 is a valid CAS Registry Number.

686722-16-7Downstream Products

686722-16-7Relevant articles and documents

Synthesis of homoceramides, novel ceramide analogues, and their lack of effect on the growth of hippocampal neurons

De Jonghe, Steven,Lamote, Inge,Venkataraman, Krishnan,Boldin, Swetlana A.,Hillaert, Ulrik,Rozenski, Jef,Hendrix, Chris,Busson, Roger,De Keukeleire, Denis,Van Calenbergh, Serge,Futerman, Anthony H.,Herdewijn, Piet

, p. 988 - 996 (2002)

The synthesis of a new series of D-erythro-homoceramide analogues is described. Several synthetic approaches were investigated. Homoceramides can be successfully synthesized from L-homoserine as chiral building block and a protected Weinreb-amide as a key intermediate. The synthesis of short-chain analogues with a heptyl side chain, as well as with a phenyl residue in the sphingoid part (instead of the naturally occurring tridecyl side chain), was effected. The homoceramides 15-17 and 24 were investigated for their potential to reverse the inhibitory effect of fumonisin B1 on axonal growth. Unfortunately, none of the tested compounds showed any biological activity due to their lack of metabolism to glucosylhomoceramide.

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