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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:
59528-27-7
Molecular Weight:
269.51
MDL number:
MFCD04039324
UNSPSC Code:
12352100
PubChem Substance ID:
24881671
NACRES:
NA.22

Quality Level

100

Assay

95%

mp

299-303 °C (lit.)

functional group

amine
iodo

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 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

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Certificates of Analysis (COA)

Lot/Batch Number
MKCW7770
MKCQ4088
MKCG2680
MKBS9592V
MKBR5463V

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Venkateswara R Narreddula et al.
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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
"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)

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