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CAS

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1373758-76-9

tert-butyl[(2R,4R)-2,4-dimethylhexyloxy]diphenylsilane is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1373758-76-9 Structure

  • Basic information

    1. Product Name: tert-butyl[(2R,4R)-2,4-dimethylhexyloxy]diphenylsilane
    2. Synonyms: tert-butyl[(2R,4R)-2,4-dimethylhexyloxy]diphenylsilane
    3. CAS NO:1373758-76-9
    4. Molecular Formula:
    5. Molecular Weight: 368.635
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1373758-76-9.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[(2R,4R)-2,4-dimethylhexyloxy]diphenylsilane(CAS DataBase Reference)
    10. NIST Chemistry Reference: tert-butyl[(2R,4R)-2,4-dimethylhexyloxy]diphenylsilane(1373758-76-9)
    11. EPA Substance Registry System: tert-butyl[(2R,4R)-2,4-dimethylhexyloxy]diphenylsilane(1373758-76-9)

  • 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: 1373758-76-9(Hazardous Substances Data)

1373758-76-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1373758-76-9 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,7,3,7,5 and 8 respectively; the second part has 2 digits, 7 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 1373758-76:
(9*1)+(8*3)+(7*7)+(6*3)+(5*7)+(4*5)+(3*8)+(2*7)+(1*6)=199
199 % 10 = 9
So 1373758-76-9 is a valid CAS Registry Number.

1373758-76-9Relevant articles and documents

Chemoenzymatic approach to the total synthesis of (+)-bourgeanic acid

Yadav, Jhillu S.,Rao, Tenneti Srinivasa,Yadav, Nagendra Nath,Rao, Kovvuru V. Raghavendra,Reddy, Basi V. Subba,Al Khazim Al Ghamdi, Ahmad

, p. 788 - 792 (2012)

A highly stereoselective total synthesis of (+)-bourgeanic acid has been accomplished by an enzymatic desymmetrization approach to create two methyl chiral centers. Other key steps involved in this approach are a Wittig reaction, a Gilman reaction, and TE

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