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83917-81-1

5-Methoxy-3-methyl-4-phenyl-2(5H)-furanone is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 83917-81-1 Structure

  • Basic information

    1. Product Name: 5-Methoxy-3-methyl-4-phenyl-2(5H)-furanone
    2. Synonyms: 5-Methoxy-3-methyl-4-phenyl-2(5H)-furanone
    3. CAS NO:83917-81-1
    4. Molecular Formula:
    5. Molecular Weight: 204.225
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 83917-81-1.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: 5-Methoxy-3-methyl-4-phenyl-2(5H)-furanone(CAS DataBase Reference)
    10. NIST Chemistry Reference: 5-Methoxy-3-methyl-4-phenyl-2(5H)-furanone(83917-81-1)
    11. EPA Substance Registry System: 5-Methoxy-3-methyl-4-phenyl-2(5H)-furanone(83917-81-1)

  • 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: 83917-81-1(Hazardous Substances Data)

83917-81-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 83917-81-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,3,9,1 and 7 respectively; the second part has 2 digits, 8 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 83917-81:
(7*8)+(6*3)+(5*9)+(4*1)+(3*7)+(2*8)+(1*1)=161
161 % 10 = 1
So 83917-81-1 is a valid CAS Registry Number.

83917-81-1Downstream Products

83917-81-1Relevant articles and documents

Rhodium Carbonyl Catalyzed Carbonylation of Unsaturated Compounds. 2. Synthesis of 5-Alkoxy-2(5H)-furanones by the Carbonylation of Acetylenes in Alcohol

Mise, Takaya,Hong, Pangbu,Yamazaki, Hiroshi

, p. 238 - 242 (2007/10/02)

The carbonylation of diphenylacetylene (1a) in ethanol in the presence of Rh4(CO)12/Na2CO3 as a catalyst gave 5-ethoxy-3,4-diphenyl-2(5H)-furanone (3b) in a 72percent yield, together with 3-(ethoxycarbonyl)-2-phenylindanone (11percent) and diethyl 2,3-dip

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