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141023-09-8

2(5H)-Furanone, 5-(2,2,2-trifluoro-1-hydroxyethyl)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 141023-09-8 Structure

  • Basic information

    1. Product Name: 2(5H)-Furanone, 5-(2,2,2-trifluoro-1-hydroxyethyl)-
    2. Synonyms:
    3. CAS NO:141023-09-8
    4. Molecular Formula: C6H5F3O3
    5. Molecular Weight: 182.099
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 141023-09-8.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: 2(5H)-Furanone, 5-(2,2,2-trifluoro-1-hydroxyethyl)-(CAS DataBase Reference)
    10. NIST Chemistry Reference: 2(5H)-Furanone, 5-(2,2,2-trifluoro-1-hydroxyethyl)-(141023-09-8)
    11. EPA Substance Registry System: 2(5H)-Furanone, 5-(2,2,2-trifluoro-1-hydroxyethyl)-(141023-09-8)

  • 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: 141023-09-8(Hazardous Substances Data)

141023-09-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 141023-09-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,1,0,2 and 3 respectively; the second part has 2 digits, 0 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 141023-09:
(8*1)+(7*4)+(6*1)+(5*0)+(4*2)+(3*3)+(2*0)+(1*9)=68
68 % 10 = 8
So 141023-09-8 is a valid CAS Registry Number.

141023-09-8Downstream Products

141023-09-8Relevant articles and documents

Facile Synthesis of α-Trifluoromethylated Alcohols from Trifluoroacetaldehyde Ethyl Hemiacetal

Kubota, Toshio,Iijima, Masahiro,Tanaka, Tatsuo

, p. 1351 - 1354 (1992)

Trifluoroacetaldehyde ethyl hemiacetal reacted with nucleophilic organosilanes such as cyanotrimethylsilane, allyltrimethylsilane, or enol trimethylsilyl ethers in the presence of Lewis acid to afford a series of α-trifluoromethylated alcohols in high yield. Key Words: trifluoroacetaldehyde ethyl hemiacetal; Lewis acid; trimethylsilylated nucleophiles; carbon-carbon bond formation; α-trifluoromethylated alcohol.

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