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(2-chlorophenyl)(phenylethynyl)sulfane is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1384843-81-5 Structure
  • Basic information

    1. Product Name: (2-chlorophenyl)(phenylethynyl)sulfane
    2. Synonyms: (2-chlorophenyl)(phenylethynyl)sulfane
    3. CAS NO:1384843-81-5
    4. Molecular Formula:
    5. Molecular Weight: 244.744
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1384843-81-5.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-chlorophenyl)(phenylethynyl)sulfane(CAS DataBase Reference)
    10. NIST Chemistry Reference: (2-chlorophenyl)(phenylethynyl)sulfane(1384843-81-5)
    11. EPA Substance Registry System: (2-chlorophenyl)(phenylethynyl)sulfane(1384843-81-5)
  • 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: 1384843-81-5(Hazardous Substances Data)

1384843-81-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1384843-81-5 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,8,4,8,4 and 3 respectively; the second part has 2 digits, 8 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 1384843-81:
(9*1)+(8*3)+(7*8)+(6*4)+(5*8)+(4*4)+(3*3)+(2*8)+(1*1)=195
195 % 10 = 5
So 1384843-81-5 is a valid CAS Registry Number.

1384843-81-5Downstream Products

1384843-81-5Relevant articles and documents

Ru-Catalyzed [3 + 2] Cycloaddition of Nitrile Oxides and Electron-Rich Alkynes with Reversed Regioselectivity

Feng, Qiang,Huang, Hai,Sun, Jianwei

, p. 2431 - 2436 (2021)

Polarity reversal ("umpolung") of a functional group can override its inherent reactivity and lead to distinct bond-forming modes. Herein we describe a rarely studied cycloaddition between nitrile oxides and electron-rich alkynes with reversed regioselect

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