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CAS

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132509-30-9

4-phenyl-2-(trimethylsilyl)pent-1-ene is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 132509-30-9 Structure

  • Basic information

    1. Product Name: 4-phenyl-2-(trimethylsilyl)pent-1-ene
    2. Synonyms:
    3. CAS NO:132509-30-9
    4. Molecular Formula:
    5. Molecular Weight: 218.414
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 132509-30-9.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: 4-phenyl-2-(trimethylsilyl)pent-1-ene(CAS DataBase Reference)
    10. NIST Chemistry Reference: 4-phenyl-2-(trimethylsilyl)pent-1-ene(132509-30-9)
    11. EPA Substance Registry System: 4-phenyl-2-(trimethylsilyl)pent-1-ene(132509-30-9)

  • 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: 132509-30-9(Hazardous Substances Data)

132509-30-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 132509-30-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,2,5,0 and 9 respectively; the second part has 2 digits, 3 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 132509-30:
(8*1)+(7*3)+(6*2)+(5*5)+(4*0)+(3*9)+(2*3)+(1*0)=99
99 % 10 = 9
So 132509-30-9 is a valid CAS Registry Number.

132509-30-9Downstream Products

132509-30-9Relevant articles and documents

The Hydroboration of (Trimethylsilyl)ethyne with Dialkylboranes and its Application to the Synthesis of (E)-1-(Trimethylsilyl)alk-1-enes and 2-(Trimethylsilyl)alk-1-enes

Hoshi, Masayuki,Masuda, Yuzuru,Arase, Akira

, p. 3237 - 3241 (1990)

The reaction of (trimethylsilyl)ethyne 1 with a stoicheiometric amount of dialkylborane 2 proceeds to the monohydroboration stage, giving a mixture of regioisomers, (E)-dialkylborane 3 and dialkylborane 4.In the hydroboration with bulky dialkylboranes, derived from internal alkenes, the former predominates.Successive treatment of the mixture with methyllithium and benzenesulphenyl chloride exclusively affords highly pure (E)-2-alkyl-1-(trimethylsily)ethene 6 whose alkyl group migrates from the boron atom, while in the hydroboration with less bulky dialkylboranes, derived from terminal alkenes, the latter predominates.Successive treatment of the mixture with aq.NaOH and iodine exclusively affords highly pure 2-(trimethylsilyl)alk-1-ene 7 whose alkyl group migrates from the boron atom.

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