跳转至内容
Merck
CN

499900

Sigma-Aldrich

2-醛基噻吩-3-硼酸

≥95%

别名:

2-甲酰基噻吩-3-硼酸

登录查看公司和协议定价


About This Item

经验公式(希尔记法):
C5H5BO3S
CAS号:
分子量:
155.97
MDL编号:
UNSPSC代码:
12352103
PubChem化学物质编号:
NACRES:
NA.22

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

从最新的版本中选择一种:

分析证书(COA)

Lot/Batch Number

没有发现合适的版本?

如果您需要特殊版本,可通过批号或批次号查找具体证书。

已有该产品?

在文件库中查找您最近购买产品的文档。

访问文档库

Synthesis of biheteroaryl derivatives by tetraphosphine/palladium-catalysed Suzuki coupling of heteroaryl bromides with heteroarylboronic acids
Kondolff I, et al.
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
Kubozono Y, et al.
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
Pellicciari R, et al.
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.

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.

联系技术服务部门