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1093350-56-1

3-(4-fluorophenylsulfanyl)pent-2-enoic acid methyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1093350-56-1 Structure

  • Basic information

    1. Product Name: 3-(4-fluorophenylsulfanyl)pent-2-enoic acid methyl ester
    2. Synonyms: 3-(4-fluorophenylsulfanyl)pent-2-enoic acid methyl ester
    3. CAS NO:1093350-56-1
    4. Molecular Formula:
    5. Molecular Weight: 240.298
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1093350-56-1.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: 3-(4-fluorophenylsulfanyl)pent-2-enoic acid methyl ester(CAS DataBase Reference)
    10. NIST Chemistry Reference: 3-(4-fluorophenylsulfanyl)pent-2-enoic acid methyl ester(1093350-56-1)
    11. EPA Substance Registry System: 3-(4-fluorophenylsulfanyl)pent-2-enoic acid methyl ester(1093350-56-1)

  • 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: 1093350-56-1(Hazardous Substances Data)

1093350-56-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1093350-56-1 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,9,3,3,5 and 0 respectively; the second part has 2 digits, 5 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 1093350-56:
(9*1)+(8*0)+(7*9)+(6*3)+(5*3)+(4*5)+(3*0)+(2*5)+(1*6)=141
141 % 10 = 1
So 1093350-56-1 is a valid CAS Registry Number.

1093350-56-1Relevant articles and documents

Regioselective synthesis of 2-(Aryloxythio)benzoates by the first [3+3] cyclizations of 3-aryloxythio-1-silyloxybuta-1,3-dienes with 3-alkoxy-2-en-1-ones

Iqbal, Inam,Imran, Muhammad,Villinger, Alexander,Langer, Peter

, p. 297 - 305 (2009)

Functionalized 2-(aryloxythio)benzoates were regio-selectively prepared by the first [3+3] cyclizations of 3-aryloxythio-1-trimethylsilyloxybuta-1,3-dienes with 3-alkoxy-2-en-1-ones. Georg Thieme Verlag Stuttgart · New York.

Synthesis of functionalized 2-(arylthio)benzoates by formal [3+3] cyclizations of 3-arylthio-1-silyloxy-1,3-butadienes with 3-silyloxy-2-en-1-ones and 1,3-diacylcyclopropanes

Iqbal, Inam,Imran, Muhammad,Rasool, Nasir,Rashid, Muhammad A.,Hussain, Munawar,Villinger, Alexander,Fischer, Christine,Langer, Peter

scheme or table, p. 7562 - 7572 (2009/12/06)

Functionalized 2-(arylthio)benzoates are prepared by formal [3+3] cyclizations of 3-arylthio-1-trimethylsilyloxy-1,3-butadienes with 3-silyloxy-2-en-1-ones and 1,1-diacylcyclopropanes.

Regioselective synthesis of 2-(arylthio)benzoates by the first catalytic [3+3] cyclocondensations of 3-(arylthio)-1-(trimethylsilyloxy)-1,3-butadienes with 1,1,3,3-tetramethoxypropane

Imran, Muhammad,Iqbal, Inam,Rasool, Nasir,Rashid, Muhammad A.,Langer, Peter

scheme or table, p. 2708 - 2710 (2009/04/11)

2-(Arylthio)benzoates were regioselectively prepared by the first catalytic [3+3] cyclizations of 3-(arylthio)-1-(trimethylsilyloxy)-1,3-butadienes with 1,1,3,3-tetramethoxypropane.

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