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Benzene, [2-(ethylsulfonyl)ethyl]- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 66499-26-1 Structure
  • Basic information

    1. Product Name: Benzene, [2-(ethylsulfonyl)ethyl]-
    2. Synonyms:
    3. CAS NO:66499-26-1
    4. Molecular Formula: C10H14O2S
    5. Molecular Weight: 198.286
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 66499-26-1.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: Benzene, [2-(ethylsulfonyl)ethyl]-(CAS DataBase Reference)
    10. NIST Chemistry Reference: Benzene, [2-(ethylsulfonyl)ethyl]-(66499-26-1)
    11. EPA Substance Registry System: Benzene, [2-(ethylsulfonyl)ethyl]-(66499-26-1)
  • 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: 66499-26-1(Hazardous Substances Data)

66499-26-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 66499-26-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,6,4,9 and 9 respectively; the second part has 2 digits, 2 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 66499-26:
(7*6)+(6*6)+(5*4)+(4*9)+(3*9)+(2*2)+(1*6)=171
171 % 10 = 1
So 66499-26-1 is a valid CAS Registry Number.

66499-26-1Downstream Products

66499-26-1Relevant articles and documents

General sulfone construction: Via sulfur dioxide surrogate control

Chen, Shihao,Li, Yaping,Wang, Ming,Jiang, Xuefeng

supporting information, p. 322 - 326 (2020/02/13)

A highly efficient one-step synthesis of alkyl-alkyl and aryl-alkyl sulfones with a facile combination of halides, sulfur dioxide surrogates and phosphate esters is described. When thiourea dioxide was employed as a reductive sulfur dioxide surrogate, alkyl-alkyl sulfones were obtained under transition metal free conditions. Aryl-alkyl sulfones were obtained with an extremely low catalytic loading (0.2 mol%) via altering the mask of sulfur dioxide surrogates to sodium dithionite. A phosphate ester was employed as a stable and readily available alkyl source. Notably, this protocol has been applied to the late-stage modification of natural products and bioactive molecules.

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