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(E)-5-chloro-5-(phenylsulfinyl)-2-tetradecen-4-one is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 144882-80-4 Structure
  • Basic information

    1. Product Name: (E)-5-chloro-5-(phenylsulfinyl)-2-tetradecen-4-one
    2. Synonyms:
    3. CAS NO:144882-80-4
    4. Molecular Formula:
    5. Molecular Weight: 368.968
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 144882-80-4.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)-5-chloro-5-(phenylsulfinyl)-2-tetradecen-4-one(CAS DataBase Reference)
    10. NIST Chemistry Reference: (E)-5-chloro-5-(phenylsulfinyl)-2-tetradecen-4-one(144882-80-4)
    11. EPA Substance Registry System: (E)-5-chloro-5-(phenylsulfinyl)-2-tetradecen-4-one(144882-80-4)
  • 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: 144882-80-4(Hazardous Substances Data)

144882-80-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 144882-80-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,4,8,8 and 2 respectively; the second part has 2 digits, 8 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 144882-80:
(8*1)+(7*4)+(6*4)+(5*8)+(4*8)+(3*2)+(2*8)+(1*0)=154
154 % 10 = 4
So 144882-80-4 is a valid CAS Registry Number.

144882-80-4Downstream Products

144882-80-4Relevant articles and documents

1-Haloalkyl Aryl Sulfoxides as Useful Agents in Synthesis of α-Halo Ketones: A New Synthesis of α-Halo Ketones, α-Halo α,β-Unsaturated Ketones, and α-Halo Cross Dienones from Aldehydes

Satoh, Tsuyoshi,Itoh, Norifumi,Onda, Ken-ichi,Kitoh, Yasushi,Yamakawa, Koji

, p. 2800 - 2806 (2007/10/02)

α-Halo α-sulfinyl ketones were synthesized in two steps from 1-haloalkyl aryl sulfoxides and aldehydes in high yields.Desulfinylation of the α-halo α-sulfinyl ketones was performed with ethylmagnesium bromide in ether at low temperature to afford α-halo ketones via magnesium enolates in high yields.The magnesium enolate intermediates were trapped with various electrophiles such as deuterium oxide, ethyl chloroformate, and chlorotrimethylsilane.Trapping of the magnesium enolate intermediate with carbonyl compounds afforded a new type of the directed aldol reaction.Desulfi nylation of the sulfinyl group of the α-halo α-sulfinyl ketones under thermal conditions gave α-halo α,β-unsatureted ketones or α-halo cross dienones.

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