Welcome to LookChem.com Sign In|Join Free

CAS

  • or

4387-36-4

4387-36-4

Post Buying Request

4387-36-4 Suppliers

Recommended suppliersmore

  • Product
  • FOB Price
  • Min.Order
  • Supply Ability
  • Supplier
  • Contact Supplier

4387-36-4 Usage

Description

2-Iodobenzonitrile is a nitrile compound characterized by the presence of both a cyano group and an aryl carbon-iodide bond in adjacent positions on a benzene ring. It is a yellow solid and is recognized for its excellent reactivity, making it a valuable intermediate in organic synthetic chemistry.

Uses

Used in Organic Synthesis:
2-Iodobenzonitrile is used as a key intermediate in the field of organic synthesis due to its reactivity and the presence of functional groups that facilitate various chemical reactions. Its utility in this application stems from the ability to undergo a wide range of reactions, such as the Suzuki reaction, which is a widely used method for the formation of carbon-carbon bonds.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, 2-Iodobenzonitrile is utilized as a building block for the synthesis of various medicinal compounds. Its unique structure allows for the creation of diverse drug candidates with potential therapeutic applications.
Used in Pesticide Industry:
2-Iodobenzonitrile is also employed in the development of pesticides, where its reactivity and structural features contribute to the design of effective and targeted pest control agents.
Used in Dye Industry:
2-Iodobenzonitrile finds application in the dye industry, where it serves as an intermediate for the production of various dyes with specific color properties and characteristics.
Used in Fine Chemicals:
2-Iodobenzonitrile is used as an intermediate in the synthesis of fine chemicals, which are high-purity chemicals with specialized applications in various industries, including electronics, fragrances, and flavors.

Check Digit Verification of cas no

The CAS Registry Mumber 4387-36-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,3,8 and 7 respectively; the second part has 2 digits, 3 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 4387-36:
(6*4)+(5*3)+(4*8)+(3*7)+(2*3)+(1*6)=104
104 % 10 = 4
So 4387-36-4 is a valid CAS Registry Number.
InChI:InChI=1/C7H4IN/c8-7-4-2-1-3-6(7)5-9/h1-4H

4387-36-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-Iodobenzonitrile

1.2 Other means of identification

Product number -
Other names 2-cyano-1-iodobenzene

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:4387-36-4 SDS

4387-36-4Relevant articles and documents

An Air-Stable N-Heterocyclic [PSiP] Pincer Iron Hydride and an Analogous Nitrogen Iron Hydride: Synthesis and Catalytic Dehydration of Primary Amides to Nitriles

Fenske, Dieter,Fuhr, Olaf,Li, Xiaoyan,Sun, Hongjian,Wang, Yajie,Xie, Shangqing,Zhang, Hua

, (2020/03/13)

An air-stable N-heterocyclic PSiP pincer iron hydride FeH(PMe3)2(SiPh(NCH2PPh2)2C6H4) (4) was synthesized by Si-H activation of a Ph-substituted [PSiP] pincer ligand. The analogous strong electron-donating iPr-substituted [PSiP] pincer ligand was prepared and introduced into iron complex to give an iron nitrogen complex FeH(N2)(PMe3)(SiPh(NCH2PiPr2)2C6H4) (6). Both 4 and 6 showed similar high efficiency for catalytic dehydration of primary amides to nitriles. Air-stable iron hydride 4 was the best catalyst for its stabilization and convenient preparation. A diverse range of cyano compounds including aromatic and aliphatic species was obtained in moderate to excellent yields. A plausible catalytic reaction mechanism was proposed.

6-Arylphenanthridines from Aryl o-Biaryl Ketones with 1,1,1,3,3,3-Hexamethyldisilazane and Molecular Iodine

Kobayashi, Eiji,Kishi, Atsushi,Togo, Hideo

, p. 7335 - 7347 (2019/11/22)

Warming treatment of aryl o-biaryl ketones with 1,1,1,3,3,3-hexamethyldisilazane in the presence of Sc(OTf)3 in toluene, followed by the reaction with molecular iodine and K2CO3 in a mixture of THF and methanol at 60 °C gave the corresponding 6-arylphenanthridines in good to moderate yields. The present reaction is a one-pot method for the preparation of 6-arylphenanthridines from aryl o-biaryl ketones through the cyclization of imino-nitrogen-centered radicals that were generated from N-iodo aryl o-biaryl ketimines formed from the reaction of aryl biaryl ketimines with molecular iodine.

Revealing resonance effects and intramolecular dipole interactions in the positional isomers of benzonitrile-core thermally activated delayed fluorescence materials

Kukhta, Nadzeya A.,Higginbotham, Heather F.,Matulaitis, Tomas,Danos, Andrew,Bismillah, Aisha N.,Haase, Nils,Etherington, Marc K.,Yufit, Dmitry S.,McGonigal, Paul R.,Gra?ulevi?ius, Juozas Vidas,Monkman, Andrew P.

supporting information, p. 9184 - 9194 (2019/08/08)

We report on the properties of the three positional isomers of (2,7-di-tert-butyl-9,9-dimethylacridin-10(9H)-yl)benzonitrile, which are found to have comparable donor steric environments and donor-acceptor dihedral angles. An unexpected intramolecular dip

Post a RFQ

Enter 15 to 2000 letters.Word count: 0 letters

Attach files(File Format: Jpeg, Jpg, Gif, Png, PDF, PPT, Zip, Rar,Word or Excel Maximum File Size: 3MB)

1

What can I do for you?
Get Best Price

Get Best Price for 4387-36-4