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84473-03-0

1,1-Dichloro-2-<(2-chlorocyclopropyl)ethyl>cyclopropane is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 84473-03-0 Structure

  • Basic information

    1. Product Name: 1,1-Dichloro-2-<(2-chlorocyclopropyl)ethyl>cyclopropane
    2. Synonyms:
    3. CAS NO:84473-03-0
    4. Molecular Formula:
    5. Molecular Weight: 213.534
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 84473-03-0.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: 1,1-Dichloro-2-<(2-chlorocyclopropyl)ethyl>cyclopropane(CAS DataBase Reference)
    10. NIST Chemistry Reference: 1,1-Dichloro-2-<(2-chlorocyclopropyl)ethyl>cyclopropane(84473-03-0)
    11. EPA Substance Registry System: 1,1-Dichloro-2-<(2-chlorocyclopropyl)ethyl>cyclopropane(84473-03-0)

  • 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: 84473-03-0(Hazardous Substances Data)

84473-03-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 84473-03-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,4,4,7 and 3 respectively; the second part has 2 digits, 0 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 84473-03:
(7*8)+(6*4)+(5*4)+(4*7)+(3*3)+(2*0)+(1*3)=140
140 % 10 = 0
So 84473-03-0 is a valid CAS Registry Number.

84473-03-0Downstream Products

84473-03-0Relevant articles and documents

Nonhomogeneous Phase Effect on the Generation of Carbene Radical Anions in the Birch-Type Reduction of Bis(gem-dihalocyclopropyl) Compounds

Oku, Akira,Yoshiura, Naoto,Okuda, Tomohisa

, p. 617 - 619 (2007/10/02)

The reduction of 1,2-bis(gem-dichlorocyclopropyl)ethane (5) with sodium metal (4 molar equiv with respect to 5) in a mixed solution of NH3-THF-EtOH, which separated a metallic liquid phase on mixing, gave the parent hydrocarbon product predominantly.On the other hand, analogous reduction of 5 with lithium metal, which produced a homogeneous colored solution, predominantly gave the di- and trichloro intermediate products.The unusual results of the reduction with a nonhomogeneous reductant mixture are explained in terms of a rapid and consecutive electron transfer tothe molecule which is taken into or located in the vicinity of the reductant phase. 3,3,8,8-Tetrachlorotricyclo2,4>octane behaved analogously.

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