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Merck
모든 사진(4)

주요 문서

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512125

Sigma-Aldrich

3-Pyridinylboronic acid

≥95.0%

동의어(들):

3-Pyridineboronic acid, 3-Pyridylboronic acid, Dihydroxy(3-pyridyl)borane, Pyridin-3-ylboronic acid

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모든 사진(4)

About This Item

실험식(Hill 표기법):
C5H6BNO2
CAS Number:
1692-25-7
Molecular Weight:
122.92
MDL number:
MFCD00674177
UNSPSC 코드:
12352103
PubChem Substance ID:
24873612
NACRES:
NA.22

Quality Level

100

분석

≥95.0%

형태

solid

mp

>300 °C (lit.)

SMILES string

OB(O)c1cccnc1

InChI

1S/C5H6BNO2/c8-6(9)5-2-1-3-7-4-5/h1-4,8-9H

InChI key

ABMYEXAYWZJVOV-UHFFFAOYSA-N

관련 카테고리

애플리케이션

3-Pyridinylboronic acid can be used as a reagent for:
  • Phosphine-free Suzuki-Miyaura cross-coupling reactions.
  • Regioselective Suzuki-Miyaura coupling and tandem palladium-catalyzed intramolecular aminocarbonylation and annulation.
  • N-arylation using copper acetylacetonate catalyst.
  • Copper-mediated cyanation and regioselective cyanation of electron-rich benzenes.

It can also be used to prepare:
  • New linear poly(phenylpyridyl) chains by Suzuki coupling.
  • Oligopyridyl foldamers as mimics of a-helix twist.
  • Many highly significant therapeutic enzymatic and kinase inhibitors and receptor antagonists.
  • Pyridine substituted pyridinium N-(2′-azinyl)aminides by reacting with dibromo pyridinium aminides via Suzuki coupling reaction.

기타 정보

Contains varying amounts of anhydride

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point (°F)

Not applicable

Flash Point (°C)

Not applicable

개인 보호 장비

Eyeshields, Gloves, type N95 (US)

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시험 성적서(COA)

Lot/Batch Number
MKCQ2668
MKBZ3819V
MKBW4557V
MKBR3950V
MKBD4313V

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문서 라이브러리에서 최근에 구매한 제품에 대한 문서를 찾아보세요.

문서 라이브러리 방문

Jana Sopkova-de Oliveira Santos et al.
Journal of chemical information and modeling, 52(2), 429-439 (2011-12-27)
Protein-protein interactions are central to many biological processes, from intracellular communication to cytoskeleton assembly, and therefore represent an important class of targets for new therapeutics. The most common secondary structure in natural proteins is an α-helix. Small molecules seem to
Synthesis of new linear poly(phenylpyridyl) chains
Perato, S.; et al.
Tetrahedron, 68, 1910-1917 (2012)
Justin I Montgomery et al.
Journal of medicinal chemistry, 55(4), 1662-1670 (2012-01-20)
The synthesis and biological activity of a new series of LpxC inhibitors represented by pyridone methylsulfone hydroxamate 2a is presented. Members of this series have improved solubility and free fraction when compared to compounds in the previously described biphenyl methylsulfone
Regioselective Suzuki coupling on pyridinium N-(3,5-dibromoheteroar-2-yl)aminides
M. Jose R, et al.
Tetrahedron Letters, 47, 36, 6457-6460 (2006)
Brian C Shook et al.
Journal of medicinal chemistry, 55(3), 1402-1417 (2012-01-14)
The design and characterization of two, dual adenosine A(2A)/A(1) receptor antagonists in several animal models of Parkinson's disease is described. Compound 1 was previously reported as a potential treatment for Parkinson's disease. Further characterization of 1 revealed that it was
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문서

Suzuki-Miyaura Cross-Coupling Reagents

Suzuki-Miyaura cross-coupling reaction is extensively used in organic chemistry, polymer science, and pharmaceutical industries.

자사의 과학자팀은 생명 과학, 재료 과학, 화학 합성, 크로마토그래피, 분석 및 기타 많은 영역을 포함한 모든 과학 분야에 경험이 있습니다..

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