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4-CYANOPHENYLZINC BROMIDE is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 131379-14-1 Structure
  • Basic information

    1. Product Name: 4-CYANOPHENYLZINC BROMIDE
    2. Synonyms: 4-CYANOPHENYLZINC BROMIDE;4-CYANOPHENYLZINC BROMIDE, 0.5M SOLUTION IN TETRAHYDROFURAN;4-cyanophenylzinc bromide solution;(p-Cyanophenyl)bromozinc;4-(Bromozincio)benzonitrile;Bromo(4-cyanophenyl) zinc;4-Cyanophenylzinc bromide solution 0.5 in THF;4-Cyanophenylzinc broMide, 0.5M in THF, packaged under Argon in resealable CheMSeal^t bottles
    3. CAS NO:131379-14-1
    4. Molecular Formula: C7H4BrNZn
    5. Molecular Weight: 247.41
    6. EINECS: N/A
    7. Product Categories: Alkyl;Organozinc Halides;Reike and Organozinc Reagents;Aryl;Chemical Synthesis;Organometallic Reagents;Organozinc Halides;Rieke and Organozinc Reagents
    8. Mol File: 131379-14-1.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: 1 °F
    4. Appearance: /
    5. Density: 0.98 g/mL at 25 °C
    6. Refractive Index: N/A
    7. Storage Temp.: 2-8°C
    8. Solubility: N/A
    9. Water Solubility: Reacts with water.
    10. Sensitive: Air Sensitive
    11. CAS DataBase Reference: 4-CYANOPHENYLZINC BROMIDE(CAS DataBase Reference)
    12. NIST Chemistry Reference: 4-CYANOPHENYLZINC BROMIDE(131379-14-1)
    13. EPA Substance Registry System: 4-CYANOPHENYLZINC BROMIDE(131379-14-1)
  • Safety Data

    1. Hazard Codes: F,Xn
    2. Statements: 19-22-36/38-40-36/37-14-11
    3. Safety Statements: 16-26-33-36-36/37
    4. RIDADR: UN 3399 4.3/PG 2
    5. WGK Germany: 1
    6. RTECS:
    7. HazardClass: 4.3
    8. PackingGroup: N/A
    9. Hazardous Substances Data: 131379-14-1(Hazardous Substances Data)

131379-14-1 Usage

Uses

4-Cyanophenylzinc bromide is used to produce biphenyl-4-carbonitrile.

Check Digit Verification of cas no

The CAS Registry Mumber 131379-14-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,1,3,7 and 9 respectively; the second part has 2 digits, 1 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 131379-14:
(8*1)+(7*3)+(6*1)+(5*3)+(4*7)+(3*9)+(2*1)+(1*4)=111
111 % 10 = 1
So 131379-14-1 is a valid CAS Registry Number.
InChI:InChI=1/C7H4N.BrH.Zn/c8-6-7-4-2-1-3-5-7;;/h2-5H;1H;/q;;+1/p-1/rC7H4BrNZn/c8-10-7-3-1-6(5-9)2-4-7/h1-4H

131379-14-1 Well-known Company Product Price

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  • Alfa Aesar

  • (H58211)  4-Cyanophenylzinc bromide, 0.5M in THF, packaged under Argon in resealable ChemSeal? bottles   

  • 131379-14-1

  • 50ml

  • 2327.0CNY

  • Detail
  • Aldrich

  • (520292)  4-Cyanophenylzincbromidesolution  0.5 M in THF

  • 131379-14-1

  • 520292-50ML

  • 3,051.36CNY

  • Detail

131379-14-1SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name zinc,benzonitrile,bromide

1.2 Other means of identification

Product number -
Other names Bromo(4-cyanophenyl)zinc

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:131379-14-1 SDS

131379-14-1Relevant articles and documents

Cobalt-Catalyzed Oxidative Homocoupling of Arylzinc Species

Bourne-Branchu, Yann,Moncomble, Aurélien,Corpet, Martin,Danoun, Gregory,Gosmini, Corinne

, p. 3352 - 3356 (2016/09/12)

A novel procedure for the synthesis of functionalized symmetrical biaryl compounds is described. The reaction proceeds via the oxidative homocoupling of arylzinc species formed by cobalt catalysis in the presence of air or p-benzoquinone depending on the nature of the functional group.

Cobalt-catalyzed electrophilic amination of arylzincs with N-chloroamines

Qian, Xin,Yu, Zailu,Auffrant, Audrey,Gosmini, Corinne

supporting information, p. 6225 - 6229 (2013/07/05)

Roles reversed: An efficient cobalt-catalyzed electrophilic amination of arylzinc reagents has been achieved. A variety of functionalized arylzincs and N-chloroamines were coupled under mild conditions (see scheme). Both secondary and tertiary arylamines were obtained in moderate to excellent yields. Copyright

Nickel-catalyzed enantioselective arylation of pyridinium ions: Harnessing an iminium ion activation mode

Chau, Stephen T.,Lutz, J. Patrick,Wu, Kevin,Doyle, Abigail G.

supporting information, p. 9153 - 9156 (2013/09/12)

A nickel for your thoughts.?? An enantioselective nickel-catalyzed cross-coupling between N-acylpyridinium salts and organozinc reagents is reported. The catalytic system, which is comprised of an air-stable NiII source and a chiral phosphoramidite ligand, affords 2-substituted-2,3-dihydro-4-pyridones with up to >99 % ee. Copyright

Cobalt-catalysed synthesis of highly substituted styrene derivatives via arylzincation of alkynes

Corpet, Martin,Gosmini, Corinne

supporting information, p. 11561 - 11563,3 (2012/12/12)

A new two-step procedure was developed by carbozincation of internal and terminal alkynes to synthesise highly functionalised vinylzinc bromides. Various tri and tetrasubstituted alkenes were prepared in moderate to good yields under mild reaction conditions in a stereo-selective manner. This methodology represents an interesting alternative to previously known methods. This journal is

Microwave-assisted Negishi and Kumada cross-coupling reactions of aryl chlorides

Walla, Peter,Kappe, C. Oliver

, p. 564 - 565 (2007/10/03)

Rapid Pd or Ni-catalyzed microwave-accelerated Negishi and Kumada cross-coupling reactions of aryl chlorides in solution and on solid phase are reported.

New chemical synthesis of functionalized arylzinc compounds from aromatic or thienyl bromides under mild conditions using a simple cobalt catalyst and zinc dust

Fillon, Hyacinthe,Gosmini, Corinne,Perichon, Jacques

, p. 3867 - 3870 (2007/10/03)

A new chemical method for the preparation of arylzinc intermediates is described in acetonitrile, on the basis of the activation of aryl bromides by low-valent cobalt species arising from the reduction of cobalt halide by zinc dust. This procedure allows for the synthesis of a variety of functionalized aryl- and thienylzinc species in good to excellent yields. The versatility and the simplicity of that original method represent an alternative to most known procedures.

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