100900
4-溴苯胺
97%
别名:
1-Amino-4-bromobenzene, p-Bromoaniline
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关于此项目
线性分子式:
BrC6H4NH2
化学文摘社编号:
分子量:
172.02
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
203-393-9
Beilstein/REAXYS Number:
742031
MDL number:
Assay:
97%
Form:
solid
Quality Level
assay
97%
form
solid
mp
56-62 °C (lit.)
functional group
bromo
SMILES string
Nc1ccc(Br)cc1
InChI
1S/C6H6BrN/c7-5-1-3-6(8)4-2-5/h1-4H,8H2
InChI key
WDFQBORIUYODSI-UHFFFAOYSA-N
Application
4-溴苯胺可以用作制备以下物质的起始原料：
通过制备4-溴苯重氮衍生物，它也可用于碳纳米管的表面功能化。
- 用于烯烃二羟基化的Sharpless不对称配体。
- 化学中间体，如4-溴苯叠氮化物 、4-溴亚硝基苯 、N-（4-溴苯基）-4-甲基苯磺酰胺 和4-（4-（4-甲基苯基磺酰胺基）苯基）丁酸乙酯。
通过制备4-溴苯重氮衍生物，它也可用于碳纳米管的表面功能化。
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wgk
WGK 3
signalword
Danger
Hazard Classifications
Acute Tox. 3 Dermal - Acute Tox. 3 Inhalation - Acute Tox. 4 Oral - Aquatic Acute 1 - Aquatic Chronic 1 - STOT RE 2
存储类别
6.1C - Combustible acute toxic Cat.3 / toxic compounds or compounds which causing chronic effects
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
dust mask type N95 (US), Eyeshields, Faceshields, Gloves
法规信息
危险化学品
此项目有
Nickel-catalyzed cross-coupling of aryl halides with alkyl halides: Ethyl 4-(4-(4-methylphenylsulfonamido)-phenyl) butanoate
Everson DA, et al.
Organic Syntheses, 90(17), 200-200 (2013)
Photoactive boron-nitrogen-carbon hybrids: from azo-borazines to polymeric materials
Oubaha H, et al.
The Journal of Organic Chemistry, 20(17), 4023-4035 (2019)
A triazine core for a new class of Sharpless asymmetric dihydroxylation ligands
McNamara CA, et al.
Tetrahedron Letters, 45(46), 8527-8529 (2004)
全球贸易项目编号
| 货号 | GTIN |
|---|---|
| CDS004694-100MG | 04061828914555 |
| 100900-5G | 04061838664624 |
| 100900-500G | 04061835369911 |
| 100900-100G | 04061835369904 |