Skip to Content
Merck
All Photos(1)

Key Documents

597139

Sigma-Aldrich

4-Iodobenzylamine hydrochloride

95%

Synonym(s):

(4-Iodophenyl)methanamine hydrochloride, p-Iodobenzylamine hydrochloride

Sign Into View Organizational & Contract Pricing


About This Item

Linear Formula:
IC6H4CH2NH2 · HCl
CAS Number:
Molecular Weight:
269.51
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22

Quality Level

Assay

95%

mp

299-303 °C (lit.)

SMILES string

Cl[H].NCc1ccc(I)cc1

InChI

1S/C7H8IN.ClH/c8-7-3-1-6(5-9)2-4-7;/h1-4H,5,9H2;1H

InChI key

GBJMURRFWZREHE-UHFFFAOYSA-N

Related Categories

General description

4-Iodobenzylamine hydrochloride can be synthesized in three steps from 4-iodobenzoic acid.

Application

4-Iodobenzylamine hydrochloride can react with methyl 4-bromomethyl-3-methoxycarbonyl cinnamate in the presence of triethylamine to give the corresponding cyclic amide.

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

Already Own This Product?

Find documentation for the products that you have recently purchased in the Document Library.

Visit the Document Library

"Design, synthesis, and evaluation of isoindolinone-hydroxamic acid derivatives as histone deacetylase (HDAC) inhibitors"
Lee S, et al.
Bioorganic & Medicinal Chemistry, 17(27), 4895-4900 (2007)

Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.

Contact Technical Service