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Merck

512117

Sigma-Aldrich

苯并[b]噻吩并-3-基硼酸

≥95.0%

别名:

苯并噻吩-3-硼酸

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About This Item

经验公式(希尔记法):
C8H7BO2S
分子量:
178.02
MDL號碼:
分類程式碼代碼:
12352103
PubChem物質ID:
NACRES:
NA.22

化驗

≥95.0%

mp

225-230 °C (lit.)

SMILES 字串

OB(O)c1csc2ccccc12

InChI

1S/C8H7BO2S/c10-9(11)7-5-12-8-4-2-1-3-6(7)8/h1-5,10-11H

InChI 密鑰

QVANIYYVZZLQJP-UHFFFAOYSA-N

應用

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.

其他說明

含不定量的酸酐

儲存類別代碼

11 - Combustible Solids

水污染物質分類(WGK)

WGK 3

閃點(°F)

Not applicable

閃點(°C)

Not applicable

個人防護裝備

Eyeshields, Gloves, type N95 (US)


历史批次信息供参考:

分析证书(COA)

Lot/Batch Number

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其他客户在看

Slide 1 of 1

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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)

商品

This brochure contains a comprehensive selection of boronic acids, boronic acid esters, diboron esters, and transition-metal catalysts useful for the Suzuki–Miyaura coupling reaction

This brochure contains a comprehensive selection of boronic acids, boronic acid esters, diboron esters, and transition-metal catalysts useful for the Suzuki–Miyaura coupling reaction

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