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597139

Sigma-Aldrich

4-Iodobenzylamine hydrochloride

95%

Synonym(s):

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

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About This Item

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

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

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

11 - Combustible Solids

wgk_germany

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Gloves, type N95 (US)


Certificates of Analysis (COA)

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"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)
Venkateswara R Narreddula et al.
The Analyst, 146(1), 156-169 (2020-10-31)
Ultraviolet-photodissociation (UVPD) mass spectrometry is an emerging analytical tool for structural elucidation of biomolecules including lipids. Gas phase UVPD of ionised fatty acids (FAs) can promote fragmentation that is diagnostic for molecular structure including the regiochemistry of carbon-carbon double bonds

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