499978
苯并[b]噻吩-2-基硼酸
≥95%
别名:
1-苯并噻吩-2-硼酸, 苯并噻吩-2-基硼酸, 苯并噻吩-2-硼酸
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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:
Quality Level
assay
≥95%
mp
256-260 °C (lit.)
SMILES string
OB(O)c1cc2ccccc2s1
InChI
1S/C8H7BO2S/c10-9(11)8-5-6-3-1-2-4-7(6)12-8/h1-5,10-11H
InChI key
YNCYPMUJDDXIRH-UHFFFAOYSA-N
Application
Reactant involved in:
- PDE4 inhibitors
- Chemoselective modification of oncolytic adenovirus
- Synthesis of phosphorescent sensor for quantification of copper(II) ion
- UV promoted phenanthridine syntheses
- Preparation of CYP11B1 inhibitors for treatment of cortisol dependent diseases
- Suzuki-Miyaura cross-coupling reactions
Other Notes
含不定量的酸酐
ppe
Eyeshields, Gloves, type N95 (US)
signalword
Warning
hcodes
Hazard Classifications
Acute Tox. 4 Oral - Aquatic Chronic 3
存储类别
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
商品
Suzuki-Miyaura cross-coupling reaction is extensively used in organic chemistry, polymer science, and pharmaceutical industries.
相关内容
S A Adediran et al.
Archives of biochemistry and biophysics, 614, 65-71 (2017-01-01)
O-Aryloxycarbonyl hydroxamates have previously been shown to covalently inactivate serine/amine amidohydrolases such as class C β-lactamases and a N-terminal hydrolase, the proteasome. We report here reactions between O-aryloxycarbonyl hydroxamates and another N-terminal hydrolase, penicillin acylase. O-Aryloxycarbonyl hydroxamates, as non-symmetric carbonates
Hyomin Jin et al.
Dalton transactions (Cambridge, England : 2003), 48(4), 1467-1476 (2019-01-12)
2-Phenylpyridine- and 2-(benzo[b]thiophen-2-yl)pyridine-based (ppy- and btp-based) o-carboranyl (Car1 and Car2) and their B(CH3)2-C∧N-chelated (Car1B and Car2B) compounds were prepared and fully characterised by multinuclear NMR spectroscopy and elemental analysis. The solid-state structure of Car2B was determined by single-crystal X-ray diffraction
Ju Hyoung Jo et al.
Chemistry (Weinheim an der Bergstrasse, Germany), 26(70), 16733-16754 (2020-07-07)
Herein, we report the synthesis, and photochemical and -physical properties, as well as the catalytic performance, of a series of heteroleptic IrIII photosensitizers (IrPSs), [Ir(C^N)2 (N^NAryl )]+ , possessing ancillary ligands that are varied with aryl-substituents on bipyridyl unit [C^N=(2-pyridyl)benzo[b]thiophen-3-yl
全球贸易项目编号
| 货号 | GTIN |
|---|---|
| 499978-5G | 04061832422206 |
| 499978-25G | 04061832904986 |