推荐产品
方案
≥95%
mp
167-193 °C (lit.)
SMILES字符串
OB(O)c1ccsc1C=O
InChI
1S/C5H5BO3S/c7-3-5-4(6(8)9)1-2-10-5/h1-3,8-9H
InChI key
BBENFHSYKBYWJX-UHFFFAOYSA-N
应用
2-Formyl-3-thiopheneboronic acid can be used as:
- A substrate in the palladium-Tedicyp catalyzed Suzuki coupling reaction with different aryl bromides.
- A starting material for the synthesis of 4H-thieno[2,3-c]-isoquinolin-5-one derivatives as PARP-1 inhibitors.
- A starting material for the preparation of phenanthro-dithiophene moieties having field-effect transistor properties.
Reactant for:
- Suzuki cross-coupling reactions
- Preparation of boronic acid esters
其他说明
含不定量的酸酐
储存分类代码
11 - Combustible Solids
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
Synthesis of biheteroaryl derivatives by tetraphosphine/palladium-catalysed Suzuki coupling of heteroaryl bromides with heteroarylboronic acids
J. Mol. Catal. A: Chem., 269(1-2), 110-118 (2007)
Transistor Properties of 2, 7-Dialkyl-Substituted Phenanthro [2, 1-b: 7, 8-b′] dithiophene
Scientific reports, 6, 38535-38535 (2016)
Towards new neuroprotective agents: design and synthesis of 4H-thieno [2, 3-c] isoquinolin-5-one derivatives as potent PARP-1 inhibitors
Il Farmaco (Societa Chimica Italiana : 1989), 58(9), 851-858 (2003)
商品
Suzuki-Miyaura cross-coupling reaction is extensively used in organic chemistry, polymer science, and pharmaceutical industries.
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