1150632-93-1

Basic information

• Product Name: 2-(dimethoxymethyl)pyridine-5-boronic acid pinacol ester
• Synonyms: 2-(dimethoxymethyl)pyridine-5-boronic acid pinacol ester;6-(Dimethoxymethyl)pyridine-3-boronic acid pinacol ester
• CAS NO: 1150632-93-1
• Molecular Formula: C₁₄H₂₂BNO₄
• Molecular Weight: 297.15506
• Mol File: 1150632-93-1.mol
• Article Data: 5

Chemical Properties

• Boiling Point: 343.2±42.0 °C(Predicted)
• Appearance: /
• Density: 1.07±0.1 g/cm3(Predicted)
• Storage Temp.: under inert gas (nitrogen or Argon) at 2-8°C
• PKA: 4?+-.0.31(Predicted)
• CAS DataBase Reference: 2-(dimethoxymethyl)pyridine-5-boronic acid pinacol ester(CAS DataBase Reference)
• NIST Chemistry Reference: 2-(dimethoxymethyl)pyridine-5-boronic acid pinacol ester(1150632-93-1)
• EPA Substance Registry System: 2-(dimethoxymethyl)pyridine-5-boronic acid pinacol ester(1150632-93-1)

Safety Data

• Hazardous Substances Data: 1150632-93-1(Hazardous Substances Data)

Usage

General Description

2-(dimethoxymethyl)pyridine-5-boronic acid pinacol ester is a chemical compound with the molecular formula C14H21BClNO5. It is a boronic acid pinacol ester derivative of pyridine, with two methoxy and one dimethoxy substituent on the pyridine ring. 2-(dimethoxymethyl)pyridine-5-boronic acid pinacol ester is commonly used in organic synthesis as a reagent for the Suzuki-Miyaura cross-coupling reaction, which is a widely used method for forming carbon-carbon bonds. It is also utilized in the preparation of complex organic molecules and pharmaceuticals. The presence of boronic acid and pyridine moieties in this compound makes it a versatile building block for the synthesis of various organic molecules.

Upstream product

• 1150632-94-2 5-bromo-2-(dimethoxymethyl)pyridine 
• 73183-34-3 bis(pinacol)diborane 
• 31181-90-5 5-bromo-pyridine-2-carbaldehyde 
• 223463-13-6 2-iodo-5-bromopyridine 

Downstream Products

• 1151762-00-3 4,4-difluoro-8-{3,5-bis[2-(2-(2-hydroxyethoxy)ethoxy)ethoxy]phenyl}-2,6-bis[(2-dimethoxymethyl)pyridyl-5-yl]-1,3,5,7-tetramethyl-4-bora-3a,4a-diaza-s-indacene 

Relevant articles and documents

Synthesis of -CN- linked covalent organic frameworks: Via the direct condensation of acetals and amines

We demonstrate herein a facile approach for constructing -CN- linked COFs from acetals. Three new COFs (imine-linked LZU-20, hydrazone-linked LZU-21, and azine-linked LZU-22) were synthesized by the direct condensation of dimethyl acetals and amines. All

Self-assembly of a trigonal bipyramidal architecture with stabilisation of iron in three spin states

Self-assembly and characterisation of a supramolecular trigonal bipyramidal iron cage containing an [FeIII(μ2-F)6(FeII)3]3+ star motif at its core is reported. The complex can be formed in a one step reaction using an heterotopic ligand that supports site-specific incorporation of iron in three distinct electronic configurations: low-spin FeII, high-spin FeII and high-spin FeIII, with iron(ii) tetrafluoroborate as the source of the bridging fluorides. Formation of a μ2-F bridged mixed-valence FeII-FeIII star is unprecedented. The peripheral high-spin FeII centres of the mixed-valence tetranuclear star incorporated in the iron cage are highly anisotropic and engage in F-mediated antiferromagnetic exchange with the central FeIII ion.

Fluorescent BODIPY-based Zn(II) complex as a molecular probe for selective detection of neurofibrillary tangles in the brains of Alzheimer's disease patients.

We have developed a new fluorescent binuclear Zn(II) complex for the detection of neurofibrillary tangles (NFTs) of hyperphosphorylated tau proteins, a representative hallmark of Alzheimer's disease (AD). The probe 1 incorporates a fluorescent BODIPY unit