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CAS

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150867-22-4

(E)-4-phenylpent-2-en-1-yl chloride is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 150867-22-4 Structure

  • Basic information

    1. Product Name: (E)-4-phenylpent-2-en-1-yl chloride
    2. Synonyms: (E)-4-phenylpent-2-en-1-yl chloride
    3. CAS NO:150867-22-4
    4. Molecular Formula:
    5. Molecular Weight: 180.677
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 150867-22-4.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)-4-phenylpent-2-en-1-yl chloride(CAS DataBase Reference)
    10. NIST Chemistry Reference: (E)-4-phenylpent-2-en-1-yl chloride(150867-22-4)
    11. EPA Substance Registry System: (E)-4-phenylpent-2-en-1-yl chloride(150867-22-4)

  • 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: 150867-22-4(Hazardous Substances Data)

150867-22-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 150867-22-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,5,0,8,6 and 7 respectively; the second part has 2 digits, 2 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 150867-22:
(8*1)+(7*5)+(6*0)+(5*8)+(4*6)+(3*7)+(2*2)+(1*2)=134
134 % 10 = 4
So 150867-22-4 is a valid CAS Registry Number.

150867-22-4Relevant articles and documents

Allylic and allenic halide synthesis via NbCl5- and NbBr 5-mediated alkoxide rearrangements

Ravikumar,Yao, Lihua,Fleming, Fraser F.

, p. 7294 - 7299 (2009)

(Chemical Equation Presented) Addition of NbCl5 or NbBr 5 to a series of magnesium, lithium, or potassium allylic or propargylic alkoxides directly provides allylic or allenic halides. Halogenation formally occurs through a metallahalo-[3,3] rearrangement, although concerted, ionic, and direct displacement mechanisms appear to operate competitively. Transposition of the olefin is equally effective for allylic alkoxides prepared by nucleophilic addition, deprotonation, or reduction. Experimentally, the niobium pentahalide halogenations are rapid, afford essentially pure (E)-allylic or -allenic halides after extraction, and are applicable to a range of aliphatic and aromatic alcohols, aldehydes, and ketones. 2009 American Chemical Society.

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