检测方案
98%
mp
145-148 °C (lit.)
SMILES字符串
COc1cc(CO)c(cc1OC)[N+]([O-])=O
InChI
1S/C9H11NO5/c1-14-8-3-6(5-11)7(10(12)13)4-9(8)15-2/h3-4,11H,5H2,1-2H3
InChI key
WBSCOJBVYHQOFB-UHFFFAOYSA-N
正在寻找类似产品? 访问 产品对比指南
一般描述
4，5-二甲氧基-2-硝基苄醇（6-硝基藜芦醇）是2-硝基苄醇的衍生物。据报道，它是通过木质素过氧化物酶（分离自黄孢原毛平革菌）催化的，藜芦醇（3，4-二甲氧基苄基）醇的氧化产物之一。
应用
4,5-二甲氧基-2-硝基苄醇（6-硝基藜芦醇）适用于合成4,5-二甲氧基-2-硝基苄基甲基丙烯酸酯（一种对光不稳定的单体） 和2-（4-（（4-（4,5-二甲氧基-2-硝基苄氧基）苯基）亚环己基）甲基）苯氧基）-N，N-二甲基乙胺（一种笼状环芬-OH配体）。
它可用于合成以下物质：
它可用于合成以下物质：
- 1-[[（（氯羰基）氧基]甲基]-4,5-二甲氧基-2-硝基苯
- 双（4,5-二甲氧基-2-硝基苯基）乙二醇，一种对光不稳定的保护基
- 光学敏感单体
- 硝基藜芦（NV）保护的α-羟基乙酸 (αG) (NV-αG-OH)，其是在硝基藜芦（NV）保护的α-羟基乙酸（α-G）的氰基甲基（CM）酯 (αG) (NV-αG-CM)的制备中所必须的
- 4,5-二甲氧基-2-硝基苄基-p-硝基碳酸苯酯
- 6-硝基藜芦氧羰基氯（NVOCCl），一种用于保护氨基糖中氨基功能的试剂
WGK
WGK 3
闪点(°F)
Not applicable
闪点(°C)
Not applicable
个人防护装备
Eyeshields, Gloves, type N95 (US)
法规信息
新产品
Bis (4, 5-dimethoxy-2-nitrophenyl) ethylene glycol: a new and efficient photolabile protecting group for aldehydes and ketones.
Kantevari S, et al.
Tetrahedron, 61(24), 5849-5854 (2005)
Nadezda Fomina et al.
Journal of the American Chemical Society, 132(28), 9540-9542 (2010-06-24)
A new light-sensitive polymer containing multiple light-sensitive triggering groups along the backbone and incorporating a quinone-methide self-immolative moiety was developed and formulated into nanoparticles encapsulating a model pharmaceutical Nile Red. Triggered burst release of the payload upon irradiation and subsequent
Andrew A Brown et al.
Langmuir : the ACS journal of surfaces and colloids, 25(3), 1744-1749 (2009-01-10)
The use of photolabile protecting groups (PGs) as a means to create latent hydrophilic surfaces is presented. Naturally hydrophobic PGs, based on o-nitrobenzyl chemistry, are used on polymer side chains, poised for cleavage upon exposure to UV light. Removal of
Alan R Katritzky et al.
The Journal of organic chemistry, 68(23), 9100-9104 (2003-11-08)
Molecules were prepared with substituted nitrobenzyl groups covalently bonded to N-(4-hydroxy-3-methoxybenzyl)acetamide (2) by ether or carbonate linkages. These compounds decomposed under irradiation at 363 nm. Those with carbonate linkages decomposed at slower rates than those with ether linkages. Molecules with
Photosensitive protecting groups of amino sugars and their use in glycoside synthesis. 2-nitrobenzyloxycarbonylamino and 6-nitroveratryloxycarbonylamino derivatives.
Amit B, et al.
The Journal of Organic Chemistry, 39(2), 192-196 (1974)
我们的科学家团队拥有各种研究领域经验，包括生命科学、材料科学、化学合成、色谱、分析及许多其他领域.
联系技术服务部门