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2-(dimethoxymethyl)pyridine-5-boronic acid pinacol ester is a chemical compound characterized by the molecular formula C14H21BClNO5. It is a boronic acid pinacol ester derivative of pyridine, featuring two methoxy and one dimethoxy substituent on the pyridine ring. 2-(dimethoxymethyl)pyridine-5-boronic acid pinacol ester is recognized for its versatility in organic synthesis, particularly as a reagent in the Suzuki-Miyaura cross-coupling reaction, a method pivotal for the formation of carbon-carbon bonds. Its unique structure, incorporating both boronic acid and pyridine moieties, positions it as a valuable building block in the synthesis of a diverse array of organic molecules and pharmaceuticals.

1150632-93-1

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  • 2-(Dimethoxymethyl)-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyridine

    Cas No: 1150632-93-1

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1150632-93-1 Usage

Uses

Used in Organic Synthesis:
2-(dimethoxymethyl)pyridine-5-boronic acid pinacol ester is used as a reagent in the Suzuki-Miyaura cross-coupling reaction for the formation of carbon-carbon bonds. Its role in this reaction is crucial for the synthesis of complex organic molecules, given the broad applicability of the Suzuki-Miyaura method in creating new carbon-carbon linkages.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, 2-(dimethoxymethyl)pyridine-5-boronic acid pinacol ester is utilized as a building block for the preparation of complex organic molecules and pharmaceuticals. Its structural features make it a key component in the development of new drugs, potentially contributing to the advancement of medicinal chemistry.
Used in Research and Development:
2-(dimethoxymethyl)pyridine-5-boronic acid pinacol ester is also employed in research and development settings, where its unique properties are explored for new applications and to enhance existing synthetic methodologies. Its presence in the lab allows chemists to experiment with novel reactions and pathways, potentially leading to breakthroughs in chemical synthesis and compound design.

Check Digit Verification of cas no

The CAS Registry Mumber 1150632-93-1 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,1,5,0,6,3 and 2 respectively; the second part has 2 digits, 9 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 1150632-93:
(9*1)+(8*1)+(7*5)+(6*0)+(5*6)+(4*3)+(3*2)+(2*9)+(1*3)=121
121 % 10 = 1
So 1150632-93-1 is a valid CAS Registry Number.

1150632-93-1SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-(dimethoxymethyl)-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyridine

1.2 Other means of identification

Product number -
Other names -

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
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More Details:1150632-93-1 SDS

1150632-93-1Relevant articles and documents

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

Li, Zhi-Jun,Ding, San-Yuan,Xue, Hua-Dong,Cao, Wei,Wang, Wei

, p. 7217 - 7220 (2016)

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

An Autocatalytic System of Photooxidation-Driven Substitution Reactions on a FeII4L6 Cage Framework

Neelakandan, Prakash P.,Jiménez, Azucena,Thoburn, John D.,Nitschke, Jonathan R.

, p. 14378 - 14382 (2015)

The functions of life are accomplished by systems exhibiting nonlinear kinetics: autocatalysis, in particular, is integral to the signal amplification that allows for biological information processing. Novel synthetic autocatalytic systems provide a foundation for the design of artificial chemical networks capable of carrying out complex functions. Here we report a set of FeII4L6 cages containing BODIPY chromophores having tuneable photosensitizing properties. Electron-rich anilines were observed to displace electron-deficient anilines at the dynamic-covalent imine bonds of these cages. When iodoaniline residues were incorporated, heavy-atom effects led to enhanced 1O2 production. The incorporation of (methylthio)aniline residues into a cage allowed for the design of an autocatalytic system: oxidation of the methylthio groups into sulfoxides make them electron-deficient and allows their displacement by iodoanilines, generating a better photocatalyst and accelerating the reaction.

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

Borilovi?, Ivana,Riddell, Imogen A.,Taylor, Lauren L. K.,Tuna, Floriana,Vitorica-Yrezabal, I?igo J.

, p. 11252 - 11255 (2021/11/04)

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.

VINYL COMPOUNDS AS FGFR AND VEGFR INHIBITORS

-

, (2018/06/23)

FGFR and VEGFR inhibitors are provided, and compounds represented by formula (1) or formula (II) as FGFR and VEGFR inhibitors, pharmaceutically acceptable salts or tautomers thereof are specifically disclosed.

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

Ojida, Akio,Sakamoto, Takashi,Inoue, Masa-Aki,Fujishima, Sho-hei,Lippens, Guy,Hamachi, Itaru

supporting information; experimental part, p. 6543 - 6548 (2009/09/26)

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

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