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Merck
CN

597139

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
NACRES:
NA.22
PubChem Substance ID:
UNSPSC Code:
12352100
MDL number:
Assay:
95%
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InChI

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

SMILES string

Cl[H].NCc1ccc(I)cc1

InChI key

GBJMURRFWZREHE-UHFFFAOYSA-N

assay

95%

mp

299-303 °C (lit.)

functional group

amine, iodo

Quality Level

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

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Gloves, type N95 (US)


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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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