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163977-20-6

2-cyanobenzyl cyanide anion is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 163977-20-6 Structure

  • Basic information

    1. Product Name: 2-cyanobenzyl cyanide anion
    2. Synonyms: 2-cyanobenzyl cyanide anion
    3. CAS NO:163977-20-6
    4. Molecular Formula:
    5. Molecular Weight: 141.152
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 163977-20-6.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-cyanobenzyl cyanide anion(CAS DataBase Reference)
    10. NIST Chemistry Reference: 2-cyanobenzyl cyanide anion(163977-20-6)
    11. EPA Substance Registry System: 2-cyanobenzyl cyanide anion(163977-20-6)

  • 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: 163977-20-6(Hazardous Substances Data)

163977-20-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 163977-20-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,6,3,9,7 and 7 respectively; the second part has 2 digits, 2 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 163977-20:
(8*1)+(7*6)+(6*3)+(5*9)+(4*7)+(3*7)+(2*2)+(1*0)=166
166 % 10 = 6
So 163977-20-6 is a valid CAS Registry Number.

163977-20-6Relevant articles and documents

Intrinsic Reactivities of Some Carbanions in ?-Adduct Forming Reactions

Crampton, Michael R.,Stevens, Andrew J.

, p. 1715 - 1720 (2007/10/02)

Kinetic and equilibrium data are reported for nucleophilic attack in methanol at unsubstituted ringpositions of 1,3,5-trinitrobenzene, 2,4,6-trinitrotoluene and 1-chloro-2,4,6-trinitrobenzene by carbanions derived from dimethyl malonate, ethyl cyanoacetate and 4-nitro-, 4-cyano- and 2-cyanobenzyl cyanides.The results are used to determine intrinsic reactivities for the carbanions in these ?-adduct forming reactions and are discussed in terms of the electronic and solvent reorganisation occurring during reaction.

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