597139
4-碘苄胺 盐酸盐
95%
别名:
(4-Iodophenyl)methanamine hydrochloride, p-Iodobenzylamine hydrochloride
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线性分子式:
IC6H4CH2NH2 · HCl
化学文摘社编号:
分子量:
269.51
NACRES:
NA.22
PubChem Substance ID:
UNSPSC Code:
12352100
MDL number:
Assay:
95%
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.
存储类别
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Eyeshields, Gloves, type N95 (US)
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
"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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