4-Iodophenylacetonitrile, 97%

CAS: 51628-12-7 | C8H6IN | 243.047 g/mol

Catalog Number	Quantity
L15119.03 also known as L15119-03	1 g

Catalog number L15119.03

also known as L15119-03

Price (USD)

Quantity:

Request bulk or custom format

Chemical Identifiers

CAS51628-12-7

IUPAC Name2-(4-iodophenyl)acetonitrile

Molecular FormulaC8H6IN

InChI KeyPNXWQTYSBFGIFD-UHFFFAOYSA-N

SMILESIC1=CC=C(CC#N)C=C1

Specifications

Appearance (Color)White to cream or yellow

Assay (GC)> 96.0%

FormCrystalline or fused solid or powder

4-Iodophenylacetonitrile is used as an intermediate in organic syntheses and in pharmaceuticals.

This Thermo Scientific Chemicals brand product was originally part of the Alfa Aesar product portfolio. Some documentation and label information may refer to the legacy brand. The original Alfa Aesar product / item code or SKU reference has not changed as a part of the brand transition to Thermo Scientific Chemicals.

Applications
4-Iodophenylacetonitrile is used as an intermediate in organic syntheses and in pharmaceuticals.

Solubility
Insoluble in water

Notes
Store in cool place. Keep container tightly closed in a dry and well-ventilated place. It is sensitive to moisture. Incompatible with oxidizing agents.

RUO – Research Use Only

General References:

Steven K. Pollack.; Jawad Naciri.; John Mastrangelo.; Charles H. Patterson.; Johnny Torres.; Martin Moore.; Ranganathan Shashidhar.; James G. Kushmerick. Sequential Deprotection for Control of Orientation in the Self-Assembly of Asymmetric Molecules for Molecular Electronic Devices. Langmuir. 2004, 20 (5), 1838-1842.
Jeremy J. Clemens.; Juliana L. Asgian.; Brett B. Busch.; Timothy Coon.; Justin Ernst.; Leonard Kaljevic.; Paul J. Krenitsky.; Timothy D. Neubert.; Edwin J. Schweiger.; Andreas Termin.; Dean Stamos. Diastereoselective One-Pot Knoevenagel Condensation/Corey-Chaykovsky Cyclopropanation. J. Org. Chem. 2013, 78 (2), 780-785.