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1283068-16-5

(E)-tert-butyl 6-hydroxy-9-phenyl-8-nonenoate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1283068-16-5 Structure

  • Basic information

    1. Product Name: (E)-tert-butyl 6-hydroxy-9-phenyl-8-nonenoate
    2. Synonyms:
    3. CAS NO:1283068-16-5
    4. Molecular Formula:
    5. Molecular Weight: 304.43
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1283068-16-5.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: (E)-tert-butyl 6-hydroxy-9-phenyl-8-nonenoate(CAS DataBase Reference)
    10. NIST Chemistry Reference: (E)-tert-butyl 6-hydroxy-9-phenyl-8-nonenoate(1283068-16-5)
    11. EPA Substance Registry System: (E)-tert-butyl 6-hydroxy-9-phenyl-8-nonenoate(1283068-16-5)

  • 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: 1283068-16-5(Hazardous Substances Data)

1283068-16-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1283068-16-5 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,8,3,0,6 and 8 respectively; the second part has 2 digits, 1 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 1283068-16:
(9*1)+(8*2)+(7*8)+(6*3)+(5*0)+(4*6)+(3*8)+(2*1)+(1*6)=155
155 % 10 = 5
So 1283068-16-5 is a valid CAS Registry Number.

1283068-16-5Downstream Products

1283068-16-5Relevant articles and documents

Titanium-mediated oxidative arylation of homoallylic alcohols

Lee, Kathleen S.,Ready, Joseph M.

, p. 2111 - 2114 (2011/04/23)

E-Substituted styrene derivatives are synthesized from terminal olefins and aryl Grignard reagents through TiIV-mediated oxidative coupling (see scheme). Substrates include homoallylic alcohols containing a range of functional groups and substituted aryl Grignard reagents. The reaction may proceed through aryltitanation followed by β-hydride elimination; reductive elimination of arene occurs from a TiIVH(aryl) intermediate.

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