671576
N-苯基羟胺
≥95.0%
别名:
N -羟基苯胺, N-羟基苯胺
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关于此项目
经验公式（希尔记法）:
C6H7NO
化学文摘社编号:
分子量:
109.13
NACRES:
NA.22
PubChem Substance ID:
UNSPSC Code:
12352100
EC Number:
202-875-6
MDL number:
Assay:
≥95.0%
Form:
solid
InChI key
CKRZKMFTZCFYGB-UHFFFAOYSA-N
InChI
1S/C6H7NO/c8-7-6-4-2-1-3-5-6/h1-5,7-8H
SMILES string
ONc1ccccc1
assay
≥95.0%
form
solid
mp
80-84 °C
storage temp.
−20°C
Quality Level
Application
N-苯基羟胺作为起始材料，可用于下列合成反应：
- 通过连续3,3-重排和环脱水反应，用金催化剂与脂肪族末端炔烃进行处理，合成2-烷基吲哚。
- 通过三组分一锅催化法，与醛和 α, β不饱和醛合成异恶唑烷。
- 通过homo3+2偶极环加成反应，处理醛和环丙烷，合成四氢1,2-恶嗪。
signalword
Danger
hcodes
pcodes
Hazard Classifications
Acute Tox. 3 Oral
存储类别
6.1C - Combustible acute toxic Cat.3 / toxic compounds or compounds which causing chronic effects
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Eyeshields, Faceshields, Gloves, type P2 (EN 143) respirator cartridges
Au-catalyzed synthesis of 2-alkylindoles from N-arylhydroxylamines and terminal alkynes
Wang Y, et al.
Chemical Communications (Cambridge, England), 47(27), 7815-7817 (2011)
Copper-catalyzed amination of alkenes and ketones by phenylhydroxylamine.
Ho C-M and Lau T-C
New. J. Chem., 24(11), 859-863 (2000)
T Nohmi et al.
Mutation research, 136(3), 159-168 (1984-06-01)
Phenylhydroxylamine (PHA) and its derivatives such as monomethyl (2-Me, 3-Me, 4-Me) and dimethyl (2,3-diMe, 2,4-diMe, 2,5-diMe, 2,6-diMe, 3,4-diMe, 3,5-diMe) were tested for their mutagenicity and for their inducing ability to inactivate transforming DNA. All these compounds except PHA and 3,5-diMePHA
C C Somerville et al.
Journal of bacteriology, 177(13), 3837-3842 (1995-07-01)
Pseudomonas pseudoalcaligenes JS45 grows on nitrobenzene as a sole source of carbon, nitrogen, and energy. The catabolic pathway involves reduction to hydroxylaminobenzene followed by rearrangement to o-amino-phenol and ring fission (S. F. Nishino and J. C. Spain, Appl. Environ. Microbiol.
Vance G Nielsen et al.
Blood coagulation & fibrinolysis : an international journal in haemostasis and thrombosis, 22(8), 657-661 (2011-08-09)
Cigarette smoking is associated with plasmatic hypercoagulability, and carbon monoxide has been demonstrated to enhance coagulation by binding to a fibrinogen-bound heme. Our objective was to design and test a redox-based method to detect carboxyhemefibrinogen. Normal, pooled, citrated plasma was
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