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CAS

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144443-15-2

(E)-1-phenyl-5(R)-methyl-4(RS)-(p-tolylsulfinyl)non-3-ene is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 144443-15-2 Structure

  • Basic information

    1. Product Name: (E)-1-phenyl-5(R)-methyl-4(RS)-(p-tolylsulfinyl)non-3-ene
    2. Synonyms:
    3. CAS NO:144443-15-2
    4. Molecular Formula:
    5. Molecular Weight: 354.557
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 144443-15-2.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)-1-phenyl-5(R)-methyl-4(RS)-(p-tolylsulfinyl)non-3-ene(CAS DataBase Reference)
    10. NIST Chemistry Reference: (E)-1-phenyl-5(R)-methyl-4(RS)-(p-tolylsulfinyl)non-3-ene(144443-15-2)
    11. EPA Substance Registry System: (E)-1-phenyl-5(R)-methyl-4(RS)-(p-tolylsulfinyl)non-3-ene(144443-15-2)

  • 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: 144443-15-2(Hazardous Substances Data)

144443-15-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 144443-15-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,4,4,4 and 3 respectively; the second part has 2 digits, 1 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 144443-15:
(8*1)+(7*4)+(6*4)+(5*4)+(4*4)+(3*3)+(2*1)+(1*5)=112
112 % 10 = 2
So 144443-15-2 is a valid CAS Registry Number.

144443-15-2Downstream Products

144443-15-2Relevant articles and documents

Enantioselective Carbon-Carbon Bond Formation via SN2 Displacements of Acyclic Allylic Mesylates

Marino, Joseph P.,Viso, Alma,Lee, Jae-Don,De La Pradilla, Roberto Fernandez,Fernandez, Paloma,Rubio, M. Belen

, p. 645 - 653 (1997)

The copper-mediated SN2′ displacement of enantiomerically pure allylic mesyloxy vinyl sulfoxides takes place with high yields and stereoselectivities. In these adducts, the newly created chiral center is adjacent to a vinyl sulfoxide functionality which should allow for subsequent chirality transfer operations. Alternatively, enantiopure alkenyl sulfones and alkenes bearing an allylic stereocenter are readily available from these adducts with high geometric control. The SN2′ displacements of structurally related mesyloxy sulfides and sulfones with organocuprates have been examined. From a single enantiomer at the allylic alcohol position, the absolute configuration of the new chiral center may be controlled by adjusting the oxidation level on sulfur.

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