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38417-31-1

Benzene, 1,2-dichloro-4-(methylsulfinyl)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 38417-31-1 Structure

  • Basic information

    1. Product Name: Benzene, 1,2-dichloro-4-(methylsulfinyl)-
    2. Synonyms:
    3. CAS NO:38417-31-1
    4. Molecular Formula: C7H6Cl2OS
    5. Molecular Weight: 209.096
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 38417-31-1.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, 1,2-dichloro-4-(methylsulfinyl)-(CAS DataBase Reference)
    10. NIST Chemistry Reference: Benzene, 1,2-dichloro-4-(methylsulfinyl)-(38417-31-1)
    11. EPA Substance Registry System: Benzene, 1,2-dichloro-4-(methylsulfinyl)-(38417-31-1)

  • 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: 38417-31-1(Hazardous Substances Data)

38417-31-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 38417-31-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,8,4,1 and 7 respectively; the second part has 2 digits, 3 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 38417-31:
(7*3)+(6*8)+(5*4)+(4*1)+(3*7)+(2*3)+(1*1)=121
121 % 10 = 1
So 38417-31-1 is a valid CAS Registry Number.

38417-31-1Downstream Products

38417-31-1Relevant articles and documents

Synthesis method of sulfoxide compound

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Paragraph 0031-0033; 0083-0085, (2021/04/07)

The invention discloses a method for preparing sulfoxide derivatives with industrial application value through substituted diaryl (heterocyclic aryl) and aryl (heterocyclic aryl) alkyl sulfide compounds. Under electrochemical reaction conditions, diaryl (heterocyclic aryl) and aryl (heterocyclic aryl) alkyl sulfide compounds which are wide in source and easy to prepare and have structural diversity are used as raw materials, lithium perchlorate (LiClO4) is used as an electrolyte, acetonitrile (CH3CN) is used as a solvent, and oxygen is used as an oxidizing agent to prepare the diaryl (heterocyclic aryl) and aryl (heterocyclic aryl) alkyl sulfoxide derivatives. Compared with reported preparation methods of sulfoxide derivatives, the preparation method disclosed by the invention is green, environment-friendly, safe, energy-saving, wide in substrate application range, good in compatibility of product functional groups, easy in obtaining of raw materials and simple and convenient to operate.

Electrochemical Scalable Sulfoxidation of Sulfides with Molecular Oxygen and Water

Cheng, Zhen,Gao, Xinglian,Yao, Lingling,Wei, Zhaoxin,Qin, Guohui,Zhang, Yonghong,Wang, Bin,Xia, Yu,Abdukader, Ablimit,Xue, Fei,Jin, Weiwei,Liu, Chenjiang

, p. 3743 - 3747 (2021/07/26)

An efficient and chemoselective synthesis of sulfoxides through the electrooxidation of sulfides has been well developed. This protocol takes advantage of electricity as the terminal oxidant and of molecular oxygen and water as the oxygen atom sources. A variety of structurally diverse sulfoxide compounds are assembled in moderate to excellent yields. The scaled-up reactions at 6–20 mmol show the good practicability and application potential of this methodology. A possible free radical mechanism has been proposed to rationalize the reaction procedure.

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