193836
3-甲氧基-4-硝基苯甲醇
99%
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关于此项目
线性分子式:
CH3OC6H3(NO2)CH2OH
化学文摘社编号:
分子量:
183.16
EC 号:
MDL编号:
UNSPSC代码:
12352100
PubChem化学物质编号:
NACRES:
NA.22
方案
99%
表单
solid
mp
95-97 °C (lit.)
官能团
hydroxyl
nitro
SMILES字符串
COc1cc(CO)ccc1[N+]([O-])=O
InChI
1S/C8H9NO4/c1-13-8-4-6(5-10)2-3-7(8)9(11)12/h2-4,10H,5H2,1H3
InChI key
AADYWCBPJZAJNU-UHFFFAOYSA-N
应用
3-Methoxy-4-nitrobenzyl alcohol was used in the synthesis of:
- 3-methoxy-4-nitrobenzyl azide
- new aryl azides, (Z)-1-(3′-azido-4′-methoxyphenyl)-2-(3″,4″,5″-trimethoxyphenyl)ethane and (Z)-1-(4′-azido-3′-methoxyphenyl)-2-(3″,4″,5″-trimethoxyphenyl)ethane, potentially useful photoaffinity labeling reagents for tubulin
- 3-methoxy-4-nitrobenzaldehyde via oxidation
- 4-[3-(2-methylphenyl)ureido]-3-methoxybenzylchloride, required for syntheses of trifluoromethyl-substituted hydantoins
警示用语：
Warning
危险声明
危险分类
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
靶器官
Respiratory system
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
dust mask type N95 (US), Eyeshields, Gloves
法规信息
新产品
Jeewoo Lee et al.
Journal of medicinal chemistry, 46(14), 3116-3126 (2003-06-27)
Isosteric replacement of the phenolic hydroxyl group in potent vanilloid receptor (VR1) agonists with the alkylsulfonamido group provides a series of compounds which are effective antagonists to the action of the capsaicin on rat VR1 heterologously expressed in Chinese hamster
K G Pinney et al.
Bioorganic & medicinal chemistry, 8(10), 2417-2425 (2000-11-01)
Two new aryl azides, (Z)-1-(3'-azido-4'-methoxyphenyl)-2-(3",4",5"-trimethoxyphenyl)ethene 9 and (Z)-1-(4'-azido-3'-methoxyphenyl)-2-(3",4",5"-trimethoxyphenyl)ethene 5, modeled after the potent antitumor, antimitotic agent combretastatin A-4 (CA-4), have been prepared by chemical synthesis as potentially useful photoaffinity labeling reagents for the colchicine site on beta-tubulin. Aryl azide 9
Trifluoromethyl-substituted hydantoins, versatile building blocks for rational drug design.
Wehner V, et al.
Tetrahedron, 60(19), 4295-4302 (2004)
Can we predict reactivity for aromatic nucleophilic substitution with [18F] fluoride ion?
Rengan R, et al.
Journal of Labelled Compounds & Radiopharmaceuticals, 33(7), 563-572 (1993)
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