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156329-61-2

3-bromobicyclo<1.1.1>pentane-1-carbonitrile is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 156329-61-2 Structure

  • Basic information

    1. Product Name: 3-bromobicyclo<1.1.1>pentane-1-carbonitrile
    2. Synonyms:
    3. CAS NO:156329-61-2
    4. Molecular Formula:
    5. Molecular Weight: 172.024
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 156329-61-2.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: 3-bromobicyclo<1.1.1>pentane-1-carbonitrile(CAS DataBase Reference)
    10. NIST Chemistry Reference: 3-bromobicyclo<1.1.1>pentane-1-carbonitrile(156329-61-2)
    11. EPA Substance Registry System: 3-bromobicyclo<1.1.1>pentane-1-carbonitrile(156329-61-2)

  • 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: 156329-61-2(Hazardous Substances Data)

156329-61-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 156329-61-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,5,6,3,2 and 9 respectively; the second part has 2 digits, 6 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 156329-61:
(8*1)+(7*5)+(6*6)+(5*3)+(4*2)+(3*9)+(2*6)+(1*1)=142
142 % 10 = 2
So 156329-61-2 is a valid CAS Registry Number.

156329-61-2Downstream Products

156329-61-2Relevant articles and documents

Synthesis of Some Bridgehead-Bridgehead-Disubstituted Bicyclopentanes

Della, Ernest W.,Taylor, Dennis K.

, p. 2986 - 2996 (2007/10/02)

The synthesis of a wide variety of 1,3-disubstituted bicyclopentanes is described, with particular emphasis on the generation of a series of 3-X-substituted bicyclopentyl bromides required for solvolytic studies.Functional group manipulation at the bridgehead was readily accomplished in the majority of cases by radical processes; in some instances, transformations were effected via carbanionic-type intermediates.

PROPELLANE: REACTION WITH FREE RADICALS

Wiberg, Kenneth B.,Waddell, Sherman T.,Laidig, Keith

, p. 1553 - 1556 (2007/10/02)

Propellane is more reactive towards free radicals than bicyclobutane, and much more reactive than bicyclopentane.Therefore, the reactivity is not determined by strain energy relief or the HOMO energy.The addition of acetaldehyde is un

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