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CAS

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96720-09-1

ethyl 6-<(tert-butyldiphenylsilyl)oxy>-5(S,E)-hydroxy-2-hexenoate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 96720-09-1 Structure

  • Basic information

    1. Product Name: ethyl 6-<(tert-butyldiphenylsilyl)oxy>-5(S,E)-hydroxy-2-hexenoate
    2. Synonyms: ethyl 6-<(tert-butyldiphenylsilyl)oxy>-5(S,E)-hydroxy-2-hexenoate
    3. CAS NO:96720-09-1
    4. Molecular Formula:
    5. Molecular Weight: 412.601
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 96720-09-1.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: ethyl 6-<(tert-butyldiphenylsilyl)oxy>-5(S,E)-hydroxy-2-hexenoate(CAS DataBase Reference)
    10. NIST Chemistry Reference: ethyl 6-<(tert-butyldiphenylsilyl)oxy>-5(S,E)-hydroxy-2-hexenoate(96720-09-1)
    11. EPA Substance Registry System: ethyl 6-<(tert-butyldiphenylsilyl)oxy>-5(S,E)-hydroxy-2-hexenoate(96720-09-1)

  • 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: 96720-09-1(Hazardous Substances Data)

96720-09-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 96720-09-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,6,7,2 and 0 respectively; the second part has 2 digits, 0 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 96720-09:
(7*9)+(6*6)+(5*7)+(4*2)+(3*0)+(2*0)+(1*9)=151
151 % 10 = 1
So 96720-09-1 is a valid CAS Registry Number.

96720-09-1Relevant articles and documents

Homoallylic Chiral Induction in the Synthesis of 2,4-Disubstituted Tetrahydrofurans by Iodoetherification. Synthetic Scope and Chiral Induction Mechanism

Labelle, M.,Morton, H. E.,Guindon, Y.,Springer, J. P.

, p. 4533 - 4540 (2007/10/02)

Chiral induction generating two new stereogenic centers has been observed in the iodoetherification of optically active ethyl 5,6-dihydroxyhexenoate.Of the pour possible isomeric tetrahydrofuran products, only two were obtained in rations up to 12:1 favor

PREPARATION OF ETHYL 5(S),6-EPOXY-3(R)-(METHOXYMETHOXY)HEXANOATE: A KEY CHIRAL INTERMEDIATE FOR MEVINOLIN AND COMPACTIN.

Guindon, Yvan,Yoakim, Christiane,Bernstein, Michael A.,Morton, Howard E.

, p. 1185 - 1188 (2007/10/02)

The synthesis of Ethyl 5(S),6-Epoxy-3(R)-(methoxymethoxy)hexanoate, a key chiral synthon for the β-hydroxy-δ-lactone portion of Mevinolin and Compactin, via a regiospecific ring opening of a tetrahydrofuran derivative by dimethyboron bromide, is described.

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