跳转至内容
Merck
CN

597139

Sigma-Aldrich

4-碘苄胺 盐酸盐

95%

别名:

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

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About This Item

线性分子式:
IC6H4CH2NH2 · HCl
CAS号:
分子量:
269.51
MDL编号:
UNSPSC代码:
12352100
PubChem化学物质编号:
NACRES:
NA.22

质量水平

方案

95%

mp

299-303 °C (lit.)

官能团

amine
iodo

SMILES字符串

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

一般描述

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

应用

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

储存分类代码

11 - Combustible Solids

WGK

WGK 3

闪点(°F)

Not applicable

闪点(°C)

Not applicable

个人防护装备

Eyeshields, Gloves, type N95 (US)


从最新的版本中选择一种:

分析证书(COA)

Lot/Batch Number

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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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