144916
2-氨基-5-甲基苯酚
98%
别名:
2-羟基-4-甲基苯胺, 4-氨基-3-羟基甲苯, 6-氨基间甲酚
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关于此项目
线性分子式:
H2NC6H3(CH3)OH
化学文摘社编号:
分子量:
123.15
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
220-620-7
Beilstein/REAXYS Number:
386144
MDL number:
产品名称
2-氨基-5-甲基苯酚, 98%
InChI key
HCPJEHJGFKWRFM-UHFFFAOYSA-N
InChI
1S/C7H9NO/c1-5-2-3-6(8)7(9)4-5/h2-4,9H,8H2,1H3
SMILES string
Cc1ccc(N)c(O)c1
assay
98%
form
powder
mp
159-162 °C (lit.)
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Application
2-氨基-5-甲酚用于采用苯氧基亚胺配体进行三齿席夫碱配体和新型非茂金属催化剂的合成 。
General description
2-氨基-5-甲酚与牛血红蛋白反应生成 2-氨基-4,4α-二氢-4α-7-二甲基-3 H -吩恶嗪-3-酮，它抑制脊髓灰质炎病毒在 Vero 细胞中的增殖 。它通过经纯化的人血红蛋白转化为二氢吩恶嗪酮 。
signalword
Warning
hcodes
Hazard Classifications
Acute Tox. 4 Oral - Skin Sens. 1
存储类别
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
dust mask type N95 (US), Eyeshields, Gloves
The investigation of novel non-metallocene catalysts with phenoxy-imine ligands for ethylene (co-) polymerization.
Zhang X, et al.
Polymer International, 62(3), 419-426 (2012)
Synthesis,structural characterization and catalytic activity study of Mn(II), Fe(III), Ni(II), Cu(II) and Zn(II) complexes of quinoxaline-2-carboxalidine-2-amino-5-methylphenol: Crystal structure of the nickel (II) complex.
Sebastian M, et al.
Polyhedron, 29(15), 3014-3020 (2010)
Antiviral activity of 2-amino-4,4alpha-dihydro-4alpha-7-dimethyl-3H-phenoxazine-3-one on poliovirus.
Akiko Iwata et al.
The Tohoku journal of experimental medicine, 200(3), 161-165 (2003-10-03)
2-Amino-4,4alpha-dihydro-4alpha-7-dimethyl-3H-phenoxazine-3-one (Phx), which was produced by the reaction of bovine hemoglobin with 2-amino-5-methylphenol, inhibited the proliferation of poliovirus in Vero cells between 0.25 microg/ml and 2 microg/ml with maximal antiviral acitivity at 1 microg/ml. These results suggest that Phx may
N Sundaraganesan et al.
Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy, 67(2), 550-558 (2006-09-26)
The laser Raman and Fourier transform infrared spectra of 2-amino-5-methylphenol were recorded in the solid phase. The equilibrium geometry, harmonic vibrational frequencies, infrared intensities, Raman scattering activities, depolarization ratios and reduced masses were calculated by HF and density functional B3LYP
A Tomoda et al.
Biochimica et biophysica acta, 1117(3), 306-314 (1992-10-27)
We found that 2-amino-5-methylphenol was converted to the dihydrophenoxazinone with a reddish brown color by purified human hemoglobin, lysates of human erythrocytes, and human erythrocytes. The reddish brown compound was identified as 2-amino-4,4 alpha-dihydro-4 alpha,7-dimethyl-3H-phenoxazin-3-one by the measurement of NMR
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