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115148-06-6

2,5-dihydroxybenzoic acid 2,2,2-trichloroethyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 115148-06-6 Structure

  • Basic information

    1. Product Name: 2,5-dihydroxybenzoic acid 2,2,2-trichloroethyl ester
    2. Synonyms: 2,5-dihydroxybenzoic acid 2,2,2-trichloroethyl ester
    3. CAS NO:115148-06-6
    4. Molecular Formula:
    5. Molecular Weight: 285.511
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 115148-06-6.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: 2,5-dihydroxybenzoic acid 2,2,2-trichloroethyl ester(CAS DataBase Reference)
    10. NIST Chemistry Reference: 2,5-dihydroxybenzoic acid 2,2,2-trichloroethyl ester(115148-06-6)
    11. EPA Substance Registry System: 2,5-dihydroxybenzoic acid 2,2,2-trichloroethyl ester(115148-06-6)

  • 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: 115148-06-6(Hazardous Substances Data)

115148-06-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 115148-06-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,5,1,4 and 8 respectively; the second part has 2 digits, 0 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 115148-06:
(8*1)+(7*1)+(6*5)+(5*1)+(4*4)+(3*8)+(2*0)+(1*6)=96
96 % 10 = 6
So 115148-06-6 is a valid CAS Registry Number.

115148-06-6Relevant articles and documents

Synthesis of the cis-3a,8b-Dihydrofurobenzofuran-2(3H)-one Ring System via a Furofuran Annulation to Activated Benzoquinones

Brimble, Margaret A.,Brimble, Mark T.,Gibson, Jennifer J.

, p. 179 - 184 (1989)

The uncatalysed addition of 2-(trimethylsiloxy)furan (4) to the 1,4-benzoquinones (5a-e) containing electron-withdrawing groups at C-2 gave the cis-3a,8b-dihydrofurobenzofuran-2(3H)-ones (6a-e) in 51-76percent yields.The 1,4-benzoquinones (5f, g, h) without electron-withdrawing groups at C-2 failed to undergo the furofuran annulation, with none of the desired adducts (6f, g, h) being isolated.The carboxylic acid adduct (6i; R=CO2H) was prepared indirectly by reductive hydrolysis of either the phenacyl adduct (6e) or the trichloroethyl ester adduct (6d) using zinc in acetic acid (9).Treatment of the methyl ketone adduct (6b) with acid effected a ring opening to the corresponding (benzofuran-2-yl)acetic acid.

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