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benzyl 3-(tert-butyldimethylsiloxy)-2-hydroxypropanoate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 131711-06-3 Structure
  • Basic information

    1. Product Name: benzyl 3-(tert-butyldimethylsiloxy)-2-hydroxypropanoate
    2. Synonyms: benzyl 3-(tert-butyldimethylsiloxy)-2-hydroxypropanoate
    3. CAS NO:131711-06-3
    4. Molecular Formula:
    5. Molecular Weight: 310.466
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 131711-06-3.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 3-(tert-butyldimethylsiloxy)-2-hydroxypropanoate(CAS DataBase Reference)
    10. NIST Chemistry Reference: benzyl 3-(tert-butyldimethylsiloxy)-2-hydroxypropanoate(131711-06-3)
    11. EPA Substance Registry System: benzyl 3-(tert-butyldimethylsiloxy)-2-hydroxypropanoate(131711-06-3)
  • 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: 131711-06-3(Hazardous Substances Data)

131711-06-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 131711-06-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,1,7,1 and 1 respectively; the second part has 2 digits, 0 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 131711-06:
(8*1)+(7*3)+(6*1)+(5*7)+(4*1)+(3*1)+(2*0)+(1*6)=83
83 % 10 = 3
So 131711-06-3 is a valid CAS Registry Number.

131711-06-3Relevant articles and documents

Intermolecular Carboamination of Unactivated Alkenes

Zhang, Yu,Liu, Haidong,Tang, Luning,Tang, Hai-Jun,Wang, Lu,Zhu, Chuan,Feng, Chao

, p. 10695 - 10699 (2018)

Herein, we report the first example of group transfer radical addition of O-vinylhydroxylamine derivatives onto unactivated alkenes. By utilizing O-vinylhydroxylamine derivatives as both the N- and C-donors, this reaction enables intermolecular carboamination of unactivated alkenes in an atom economical fashion. As the process is initiated through N-radical addition followed by C-transfer, linear carboamination products are afforded. This differs from canonical radical carbofunctionalization of olefins, which typically favors branched product owing to initiation by C-radical addition.

MASKED CARBOXYLATE NEOPENTYL SULFONYL ESTER CYCLIZATION RELEASE PRODRUGS OF ACAMPROSATE, COMPOSITIONS THEREOF, AND METHODS OF USE

-

Page/Page column 51, (2009/04/24)

Masked carboxylate neopentyl sulfonyl ester prodrugs of acamprosate, pharmaceutical compositions comprising such prodrugs, and methods of using such prodrugs and compositions thereof for treating diseases are disclosed. In particular, acamprosate prodrugs

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