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118712-58-6

(2S)-glycidyl 2,4,5-trichlorobenzenesulfonate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 118712-58-6 Structure

  • Basic information

    1. Product Name: (2S)-glycidyl 2,4,5-trichlorobenzenesulfonate
    2. Synonyms:
    3. CAS NO:118712-58-6
    4. Molecular Formula:
    5. Molecular Weight: 317.577
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 118712-58-6.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: (2S)-glycidyl 2,4,5-trichlorobenzenesulfonate(CAS DataBase Reference)
    10. NIST Chemistry Reference: (2S)-glycidyl 2,4,5-trichlorobenzenesulfonate(118712-58-6)
    11. EPA Substance Registry System: (2S)-glycidyl 2,4,5-trichlorobenzenesulfonate(118712-58-6)

  • 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: 118712-58-6(Hazardous Substances Data)

118712-58-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 118712-58-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,8,7,1 and 2 respectively; the second part has 2 digits, 5 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 118712-58:
(8*1)+(7*1)+(6*8)+(5*7)+(4*1)+(3*2)+(2*5)+(1*8)=126
126 % 10 = 6
So 118712-58-6 is a valid CAS Registry Number.

118712-58-6Downstream Products

118712-58-6Relevant articles and documents

Arenesulfonate Derivatives of Homochiral Glycidol: Versatile Chiral Building Blocks for Organic Synthesis

Klunder, Janice M.,Onami, Tetsuo,Sharpless, K. Barry

, p. 1295 - 1304 (2007/10/02)

The preparation of a series of crystalline arenesulfonate derivatives of enantiomerically enriched glycidol is described.The enhancement of optical purity by recrystallization was particularly successful for two of these derivatives, glycidyl tosylate and glycidyl 3-nitrobenzenesulfonate, which were obtained in 97 percent ee and 99 percent ee, respectively.Very high regioselectivity was observed in the reactions of these compounds with a variety of nucleophiles, including aryl oxides, Et2AlCN, organometallic reagents, and BH3-NaBH4.The application of this methodology to the synthesis of homochiral β-adrenergic blocking agents and homochiral terminal epoxides is discussed.

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