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  • 130894-85-8 Structure
  • Basic information

    1. Product Name: Benzene, [2,2-dibromo-1-(bromomethyl)cyclopropyl]-
    2. Synonyms:
    3. CAS NO:130894-85-8
    4. Molecular Formula: C10H9Br3
    5. Molecular Weight: 368.893
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 130894-85-8.mol
    9. Article Data: 1
  • 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, [2,2-dibromo-1-(bromomethyl)cyclopropyl]-(CAS DataBase Reference)
    10. NIST Chemistry Reference: Benzene, [2,2-dibromo-1-(bromomethyl)cyclopropyl]-(130894-85-8)
    11. EPA Substance Registry System: Benzene, [2,2-dibromo-1-(bromomethyl)cyclopropyl]-(130894-85-8)
  • 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: 130894-85-8(Hazardous Substances Data)

130894-85-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 130894-85-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,0,8,9 and 4 respectively; the second part has 2 digits, 8 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 130894-85:
(8*1)+(7*3)+(6*0)+(5*8)+(4*9)+(3*4)+(2*8)+(1*5)=138
138 % 10 = 8
So 130894-85-8 is a valid CAS Registry Number.

130894-85-8Relevant articles and documents

Preparation of Various 1,1-Dihalo-2-haloalkylcyclopropanes and 1,1,2-Trihalocyclopropanes and their Reduction to Dihalides using Tributyltin Hydride

Pettersen, Anita,Jorgensen, Evy,Sydnes, Leiv K.

, p. 603 - 609 (2007/10/02)

The title compounds, most of which were obtained by dihalocarbene addition to the corresponding alkenes, are generally reduced to dihalides in good yields. 1,1-Dichloro-2-chloromethyl-2-methylcyclopropane and all the tribromides investigated are attacked regioselectively at the gem-dihalo moiety, yielding isomeric mixtures of 1-halo-2-haloalkylcyclopropanes.Trihalides containing both bromo and chloro substituents are always attacked at the C-Br bond; as a consequence substituted 2-bromomethyl-1,1-dichlorocyclopropanes undergo ring opening and form 4,4-dichloro-1-butene derivatives.

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