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CAS

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1036278-66-6

dimethyl (S)-4-(tert-butyldiphenylsilyloxy)-3-methylbutane-1,1-dicarboxylate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1036278-66-6 Structure

  • Basic information

    1. Product Name: dimethyl (S)-4-(tert-butyldiphenylsilyloxy)-3-methylbutane-1,1-dicarboxylate
    2. Synonyms: dimethyl (S)-4-(tert-butyldiphenylsilyloxy)-3-methylbutane-1,1-dicarboxylate
    3. CAS NO:1036278-66-6
    4. Molecular Formula:
    5. Molecular Weight: 442.627
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1036278-66-6.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: dimethyl (S)-4-(tert-butyldiphenylsilyloxy)-3-methylbutane-1,1-dicarboxylate(CAS DataBase Reference)
    10. NIST Chemistry Reference: dimethyl (S)-4-(tert-butyldiphenylsilyloxy)-3-methylbutane-1,1-dicarboxylate(1036278-66-6)
    11. EPA Substance Registry System: dimethyl (S)-4-(tert-butyldiphenylsilyloxy)-3-methylbutane-1,1-dicarboxylate(1036278-66-6)

  • 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: 1036278-66-6(Hazardous Substances Data)

1036278-66-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1036278-66-6 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,3,6,2,7 and 8 respectively; the second part has 2 digits, 6 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 1036278-66:
(9*1)+(8*0)+(7*3)+(6*6)+(5*2)+(4*7)+(3*8)+(2*6)+(1*6)=146
146 % 10 = 6
So 1036278-66-6 is a valid CAS Registry Number.

1036278-66-6Relevant articles and documents

The first enantioselective synthesis of palinurin

Perez, Manuel,Perez, Daniel I.,Martinez, Ana,Castro, Ana,Gomez, Generosa,Fall, Yagamare

supporting information; experimental part, p. 3252 - 3254 (2009/12/01)

The first enantioselective synthesis of palinurin has been accomplished starting from commercially available furaldehyde and (R)-methyl-3-hydroxy-2- methylpropionate; the key steps of the synthesis include the use of a chiral pyrrolidine to create the chiral tetronic moiety, and Horner-Wadsworth-Emmons, Wittig and Wittig-Horner reactions to construct the alkene units.

Furan derivatives, method of synthesis and uses thereof

-

Page/Page column 31, (2008/12/06)

The present invention relates to furan derivatives of formula (I), their method of synthesis and uses thereof. Concretely, the compounds disclosed have proved to be inhibitors of glycogen synthase kinase 3β, GSK-3 β, which is known to be involved in different disease and conditions, such as Alzheimer's disease or non-insulin dependent diabetes mellitus. The present invention also relates to pharmaceutical compositions comprising the same. Further, the present invention is directed to the use of the compounds in the manufacture of a medicament for the treatment and/or prevention of a GSK-3 mediated disease or condition.

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