512117
苯并[b]噻吩并-3-基硼酸
≥95.0%
别名:
苯并噻吩-3-硼酸
登录 查看组织和合同定价。
选择尺寸
关于此项目
经验公式（希尔记法）:
C8H7BO2S
化学文摘社编号:
分子量:
178.02
NACRES:
NA.22
PubChem Substance ID:
UNSPSC Code:
12352103
MDL number:
InChI
1S/C8H7BO2S/c10-9(11)7-5-12-8-4-2-1-3-6(7)8/h1-5,10-11H
SMILES string
OB(O)c1csc2ccccc12
InChI key
QVANIYYVZZLQJP-UHFFFAOYSA-N
assay
≥95.0%
mp
225-230 °C (lit.)
Quality Level
Application
Benzo[b]thien-3-ylboronic acid can be used:
- To prepare thienyl substituted pyrimidine derivatives as potent antimycobacterial compounds.
- To prepare 3-O-protected 17-heteroaryl-3-hydroxyestra-1,3,5,16-tetraene-16-carbaldehyde, which in turn is used for the synthesis of heteroarenes-annelated estranes.
- As a substrate in the study of metal-free coupling reactions of allylic alcohols with heteroaryl boronic acids.
- As a starting material for the preparation of thienyl based quinoline and pyridine ligands, which are further used to synthesize platinum complexes.
Other Notes
含不定量的酸酐
存储类别
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Eyeshields, Gloves, type N95 (US)
法规信息
新产品
此项目有
Synthesis, characterization, and photophysical properties of bismetalated platinum complexes with benzothiophene ligands
Anderson CM, et al.
Journal of Organometallic Chemistry, 882, 10-17 (2019)
Heteroareno-annelated estranes by triene cyclization
Watanabe M, et al.
open chemistry, 4(3), 375-402 (2006)
Synthesis, and structure-activity relationship for C (4) and/or C (5) thienyl substituted pyrimidines, as a new family of antimycobacterial compounds
Verbitskiy EV, et al.
European Journal of Medicinal Chemistry, 97, 225-234 (2015)
Metal-free allylation of electron-rich heteroaryl boronic acids with allylic alcohols
Li X, et al.
Tetrahedron, 72(15), 1873-1880 (2016)
商品
Suzuki-Miyaura cross-coupling reaction is extensively used in organic chemistry, polymer science, and pharmaceutical industries.
相关内容
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