779474
2-(5-Amino-2-hydroxyphenyl)benzothiazole
≥97% (HPLC)
别名:
4-Amino-2-(2-benzothiazolyl)phenol
登录查看公司和协议定价
选择尺寸
关于此项目
经验公式(希尔记法):
C13H10N2OS
化学文摘社编号:
分子量:
242.30
Beilstein:
212070
MDL编号:
UNSPSC代码:
12352200
PubChem化学物质编号:
NACRES:
NA.22
方案
≥97% (HPLC)
表单
powder
荧光
λem 465 nm±20 nm
SMILES字符串
Nc1ccc(O)c(c1)-c2nc3ccccc3s2
InChI
1S/C13H10N2OS/c14-8-5-6-11(16)9(7-8)13-15-10-3-1-2-4-12(10)17-13/h1-7,16H,14H2
InChI key
UBRCBHVOYDSGKZ-UHFFFAOYSA-N
应用
2-(5-Amino-2-hydroxyphenyl)benzothiazole is a fluorescent dye that may be used in the synthesis of a photoactive hybrid material by dispersion in a silica matrix with potential application in optical sensors. It may also be used to synthesize N-[3-(benzothiazol-2-yl)-4-hydroxyphenyl]-octanamide that shows the existence of an excited-state intramolecular proton transfer (ESIPT) process.
警示用语:
Warning
危险分类
Acute Tox. 4 Oral - 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
法规信息
新产品
此项目有
Photophysics of aminobenzazole dyes in silica-based hybrid materials.
Grando SR, et al.
Journal of Sol-Gel Science and Technology, 63(2), 235-241 (2012)
New fluorescent monomers and polymers displaying an intramolecular proton?transfer mechanism in the electronically excited state (ESIPT), 1. Synthesis of benzazolylvinylene derivatives and its copolymerization with methyl methacrylate (MMA).
Campo LF, et al.
Macromolecular Rapid Communications, 21(12), 832-836 (2000)
Luminescent properties of benzothiazole derivatives and their application in white light emission.
Lu F, et al.
Royal Society of Chemistry Advances, 7(7), 4196-4202 (2017)
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.
联系客户支持