等级
purum
方案
≥97.0% (AT)
沸点
159-162 °C/19 mmHg (lit.)
mp
76-82 °C
77-79 °C (lit.)
储存温度
2-8°C
SMILES字符串
[O-][N+](=O)c1ccc(OC(Cl)=O)cc1
InChI
1S/C7H4ClNO4/c8-7(10)13-6-3-1-5(2-4-6)9(11)12/h1-4H
InChI key
NXLNNXIXOYSCMB-UHFFFAOYSA-N
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其他说明
用于合成混合型、活性碳酸酯和硫代碳酸酯、活性聚氨酯和其他化合物的试剂
警示用语：
Danger
危险声明
危险分类
Eye Dam. 1 - Skin Corr. 1B - STOT SE 3
靶器官
Respiratory system
储存分类代码
8A - Combustible corrosive hazardous materials
WGK
WGK 3
闪点(°F)
>230.0 °F
闪点(°C)
> 110 °C
个人防护装备
Eyeshields, Faceshields, Gloves, type P3 (EN 143) respirator cartridges
D. Phillips et al.
Tetrahedron Letters, 31, 3291-3291 (1990)
Kai Dong et al.
International journal of nanomedicine, 11, 5109-5123 (2016-10-28)
In this study, a type of multifunctional mixed micelles were prepared by a novel biodegradable amphiphilic polymer (MPEG-SS-2SA) and a multidrug resistance (MDR) reversal agent (d-α-tocopheryl polyethylene glycol succinate, TPGS). The mixed micelles could achieve rapid intracellular drug release and
Zhengjie Yang et al.
Journal of orthopaedic translation, 21, 57-65 (2020-02-27)
The survival rate of osteosarcoma therapy still lags behind overall cancer therapies due to the intrinsic or acquired drug resistance. Developing novel drug delivery systems that may overcome drug resistance would greatly facilitate osteosarcoma therapy. Poly(ethylene glycol) (PEG)-sheddable reduction-sensitive polyurethane
Jingjing Pan et al.
ACS applied materials & interfaces, 6(16), 14391-14398 (2014-07-18)
In this work, a novel gene delivery strategy was proposed based on silicon nanowire arrays modified with high-molecular-weight 25 kDa branched polyethylenimine (SN-PEI). Both the plasmid DNA (pDNA) binding capacity and the in vitro gene transfection efficiency of silicon nanowire
Feng Ren et al.
Chemical & pharmaceutical bulletin, 62(9), 898-905 (2014-09-02)
A series of novel benzyloxyurea derivatives was designed, synthesized by substituting different benzyls or phenyls on N,N'-positions of the hydroxyurea (HU). These target compounds were evaluated for their anticancer activity in vitro against human leukemia cell line K562 and murine
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