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133095-96-2

(S)-5-(3-Methoxy-5-methylsulfanyl-4-propoxy-phenyl)-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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  • (S)-5-(3-Methoxy-5-methylsulfanyl-4-propoxy-phenyl)-dihydro-furan-2-one

    Cas No: 133095-96-2

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  • 133095-96-2 Structure

  • Basic information

    1. Product Name: (S)-5-(3-Methoxy-5-methylsulfanyl-4-propoxy-phenyl)-dihydro-furan-2-one
    2. Synonyms:
    3. CAS NO:133095-96-2
    4. Molecular Formula:
    5. Molecular Weight: 296.387
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 133095-96-2.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: (S)-5-(3-Methoxy-5-methylsulfanyl-4-propoxy-phenyl)-dihydro-furan-2-one(CAS DataBase Reference)
    10. NIST Chemistry Reference: (S)-5-(3-Methoxy-5-methylsulfanyl-4-propoxy-phenyl)-dihydro-furan-2-one(133095-96-2)
    11. EPA Substance Registry System: (S)-5-(3-Methoxy-5-methylsulfanyl-4-propoxy-phenyl)-dihydro-furan-2-one(133095-96-2)

  • 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: 133095-96-2(Hazardous Substances Data)

133095-96-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 133095-96-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,3,0,9 and 5 respectively; the second part has 2 digits, 9 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 133095-96:
(8*1)+(7*3)+(6*3)+(5*0)+(4*9)+(3*5)+(2*9)+(1*6)=122
122 % 10 = 2
So 133095-96-2 is a valid CAS Registry Number.

133095-96-2Relevant articles and documents

Conversion of a silylated hemiacetal into an α-bromoether using trimethylsilylbromide. Synthesis of platelet activating factor antagonist L-659,989

Thompson,Tschaen,Simpson,McSwine,Russ,Little,Verhoeven,Shinkai

, p. 6953 - 6956 (1990)

An efficient synthesis of platelet activating factor antagonist L-659,989 has been achieved in ten steps from commercially available 5-iodovanillin. The key transformation converts a silylated hemi-acetal into an α-bromoether followed by a highly stereose

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