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5-[1-Phenylsulfanyl-eth-(E)-ylidene]-dihydro-furan-2-one is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 109574-08-5 Structure
  • Basic information

    1. Product Name: 5-[1-Phenylsulfanyl-eth-(E)-ylidene]-dihydro-furan-2-one
    2. Synonyms: 5-[1-Phenylsulfanyl-eth-(E)-ylidene]-dihydro-furan-2-one
    3. CAS NO:109574-08-5
    4. Molecular Formula:
    5. Molecular Weight: 220.292
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 109574-08-5.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: 5-[1-Phenylsulfanyl-eth-(E)-ylidene]-dihydro-furan-2-one(CAS DataBase Reference)
    10. NIST Chemistry Reference: 5-[1-Phenylsulfanyl-eth-(E)-ylidene]-dihydro-furan-2-one(109574-08-5)
    11. EPA Substance Registry System: 5-[1-Phenylsulfanyl-eth-(E)-ylidene]-dihydro-furan-2-one(109574-08-5)
  • 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: 109574-08-5(Hazardous Substances Data)

109574-08-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 109574-08-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,9,5,7 and 4 respectively; the second part has 2 digits, 0 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 109574-08:
(8*1)+(7*0)+(6*9)+(5*5)+(4*7)+(3*4)+(2*0)+(1*8)=135
135 % 10 = 5
So 109574-08-5 is a valid CAS Registry Number.

109574-08-5Downstream Products

109574-08-5Relevant articles and documents

Thio- and Seleno-lactonizations of Alkynoic Acids

Toru, Takeshi,Fujita, Satoshi,Saito, Makoto,Maekawa, Eturo

, p. 1999 - 2004 (2007/10/02)

Regio- and stereo-specific thio- and seleno-lactonizations of hept-4-ynoic acid (1a), hex-4-ynoic acid (1b), and pent-4-ynoic acid (1c) can be achieved by treatment of benzenesulphenyl chloride and benzeneselenyl chloride using a hydrogen chloride capture

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