882562-39-2

Basic information

• Product Name: 1-tosyl-1H-pyrrolo[2,3-b]pyridin-3-ylboronic acid
• Synonyms: 1-tosyl-1H-pyrrolo[2,3-b]pyridin-3-ylboronic acid;Boronic acid, B-[1-[(4-methylphenyl)sulfonyl]-1H-pyrrolo[2,3-b]pyridin-3-yl]-;[1-[(4-Methylphenyl)sulfonyl]-1H-pyrrolo[2,3-b]pyridin-3-yl]boronic acid;[1-(4-methylphenyl)sulfonylpyrrolo[2,3-b]pyridin-3-yl]boronic acid;(1-Tosyl-1H-pyrrolo[2,3-b]pyridin-3-yl)
• CAS NO: 882562-39-2
• Molecular Formula: C₁₄H₁₃BN₂O₄S
• Molecular Weight: 316.14
• Product Categories: CHIRAL CHEMICALS
• Mol File: 882562-39-2.mol

Chemical Properties

• Boiling Point: 596.1°C at 760 mmHg
• Flash Point: 314.3°C
• Appearance: /
• Density: 1.39±0.1 g/cm3 (20 ºC 760 Torr)
• Vapor Pressure: 4.69E-15mmHg at 25°C
• Refractive Index: 1.647
• Storage Temp.: Inert atmosphere,Store in freezer, under -20°C
• PKA: 6.82±0.30(Predicted)
• CAS DataBase Reference: 1-tosyl-1H-pyrrolo[2,3-b]pyridin-3-ylboronic acid(CAS DataBase Reference)
• NIST Chemistry Reference: 1-tosyl-1H-pyrrolo[2,3-b]pyridin-3-ylboronic acid(882562-39-2)
• EPA Substance Registry System: 1-tosyl-1H-pyrrolo[2,3-b]pyridin-3-ylboronic acid(882562-39-2)

Safety Data

• Hazardous Substances Data: 882562-39-2(Hazardous Substances Data)

Usage

Uses

Used in Organic Synthesis:
1-tosyl-1H-pyrrolo[2,3-b]pyridin-3-ylboronic acid is used as a building block in organic synthesis for its ability to form stable complexes with certain biomolecules. This property makes it valuable in the development of pharmaceuticals and agrochemicals.
Used in Medicinal Chemistry:
In the field of medicinal chemistry, 1-tosyl-1H-pyrrolo[2,3-b]pyridin-3-ylboronic acid is utilized as a key component in the synthesis of potential drug candidates, contributing to the advancement of drug discovery.
Used in Materials Science:
1-tosyl-1H-pyrrolo[2,3-b]pyridin-3-ylboronic acid is employed in materials science for its potential applications in creating new materials with unique properties.
Used in Chemical Biology:
In chemical biology, 1-tosyl-1H-pyrrolo[2,3-b]pyridin-3-ylboronic acid serves as a valuable tool for studying biological processes due to its ability to interact with biomolecules, aiding in the understanding of complex biological systems.
Overall, 1-tosyl-1H-pyrrolo[2,3-b]pyridin-3-ylboronic acid is a multifaceted compound with a broad spectrum of applications across different industries, showcasing its significance in modern scientific research and development.

InChI:InChI=1/C14H13BN2O4S/c1-10-4-6-11(7-5-10)22(20,21)17-9-13(15(18)19)12-3-2-8-16-14(12)17/h2-9,18-19H,1H3

Upstream product

• 7732-18-5 water 
• 73183-34-3 bis(pinacol)diborane 
• 226085-18-3 3-bromo-1-(4-methylbenzenesulfonyl)-1H-pyrrolo[2,3-b]pyridine 
• 74420-15-8 3-bromo-1H-pyrrolo[2,3-b]pyridine 
• 271-63-6 7-Azaindole 
• 5419-55-6 Triisopropyl borate 
• 664982-01-8 3-iodo-1-(toluene-4-sulfonyl)-1H-pyrrolo[2,3-b]pyridine 

Downstream Products

• 1417421-80-7 (R)-2-methyl-2-(2-(1-tosyl-1H-pyrrolo[2,3-b]pyridin-3-yl)pyrimidin-4-ylamino)butanoic acid 
• 944842-54-0 decernotinib 
• 1417421-95-4 methyl 2-methyl-2-((2-(1-tosyl-1H-pyrrolo[2,3-b]pyridin-3-yl)pyrimidin-4-yl)amino)butanoate 
• 1417421-89-6 C₂₁⁽¹³⁾C₄H₂₅F₃N₄⁽¹⁵⁾N₂O₃S 
• 866545-91-7 1-(4-methylbenzenesulfonyl)-3-(tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-pyrrolo[2,3-b]pyridine 
• 1227866-35-4 4-[(3,5-difluorobenzyl)amino]-6-(1H-pyrrolo[2,3-b]pyridin-3-yl)pyridine-3-carboxyamide 
• 1227866-34-3 4-[(3,5-difluorobenzyl)amino]-6-{1-[(4-methylphenyl)sulfonyl]-1H-pyrrolo[2,3-b]pyridin-3-yl}pyridine-3-carboxyamide 

Relevant articles and documents

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