107099-99-0

Basic information

• Product Name: 2,5-Dimethoxyphenylboronic acid
• Synonyms: 2,5-DIMETHOXYPHENYLBORONIC ACID,99+%;2,5-Dimethoxyphenylboronic Acid (contains varying amounts of Anhydride);2,5-Dimethoxyphenylboronic acid ,98%;2,5-Dimethoxyphenylboronic acid,97%;2,5-Dimethoxyphenylboronic acid, May contain varying amounts of anhydride, 97%;(2,5-dimethoxyphenyl)boronic acid(SALTDATA: FREE);AKOS BRN-0036;2,5-DIMETHOXYPHENYLBORONIC ACID
• CAS NO: 107099-99-0
• Molecular Formula: C₈H₁₁BO₄
• Molecular Weight: 181.98
• EINECS: -0
• Product Categories: BoronicAcids;Boric Acid;Boronic Acid;Alkoxy;Aryl;Organoborons;B (Classes of Boron Compounds);Boronic Acids;Boronic Acids;Boronic Acids and Derivatives;blocks
• Mol File: 107099-99-0.mol
• Article Data: 17

Chemical Properties

• Melting Point: 95-98 °C(lit.)
• Boiling Point: 374.5 °C at 760 mmHg
• Flash Point: 180.3 °C
• Appearance: /solid
• Density: 1.19 g/cm³
• Vapor Pressure: 2.84E-06mmHg at 25°C
• Refractive Index: 1.517
• Storage Temp.: 0-6°C
• Solubility: soluble in Methanol
• PKA: 8.12±0.58(Predicted)
• BRN: 2969872
• CAS DataBase Reference: 2,5-Dimethoxyphenylboronic acid(CAS DataBase Reference)
• NIST Chemistry Reference: 2,5-Dimethoxyphenylboronic acid(107099-99-0)
• EPA Substance Registry System: 2,5-Dimethoxyphenylboronic acid(107099-99-0)

Safety Data

• Hazard Codes: Xi
• Statements: 36/37/38
• Safety Statements: 37/39-26-36/37-36/37/39
• WGK Germany: 3
• HazardClass: IRRITANT
• Hazardous Substances Data: 107099-99-0(Hazardous Substances Data)

Usage

Description

2,5-Dimethoxyphenylboronic acid is a white to almost white crystalline powder with unique chemical properties. It is a boronic acid derivative that has found applications in various fields due to its distinct characteristics.

Uses

Used in Chemical Synthesis:
2,5-Dimethoxyphenylboronic acid is used as a reagent in the Suzuki reaction for the formation of carbon-carbon bonds. This reaction is a widely employed method in organic chemistry for the synthesis of complex molecules, particularly in the pharmaceutical and agrochemical industries.
Used in Pharmaceutical Industry:
2,5-Dimethoxyphenylboronic acid is used as a building block for the synthesis of various pharmaceutical compounds. Its unique structure allows for the creation of new drugs with potential therapeutic applications.
Used in Environmental Applications:
2,5-Dimethoxyphenylboronic acid is used as a bacterial mutagen in environmental studies. It can help in understanding the effects of mutations on bacterial populations and their role in the ecosystem.
Used in Research and Development:
2,5-Dimethoxyphenylboronic acid is used as a research compound for studying its properties and potential applications in various fields, including material science, chemical engineering, and biotechnology.

InChI:InChI=1/C8H11BO4/c1-12-6-3-4-8(13-2)7(5-6)9(10)11/h3-5,10-11H,1-2H3

Upstream product

• 121-43-7 Trimethyl borate 
• 150-78-7 1,4-dimethoxybezene 
• 688-74-4 boric acid tributyl ester 
• 7732-18-5 water 
• 39175-16-1 2-lithio-1,4-dimethoxybenzene 
• 25245-34-5 1-bromo-2,5-dimethoxybenzene 
• 5419-55-6 Triisopropyl borate 

Downstream Products

• 18086-27-6 3-(2,5-dimethoxy-phenyl)-7-methoxy-chromen-4-one 
• 209906-24-1 [5-(2'',5''-dimethoxybiphenyl-4'-yl)-10,15-20-triphenylporphinato]zinc(II) 
• 1159770-80-5 2-(3,6-dioxocyclohexa-1,4-dienyl)-5-methoxy-7-methyl-1,4-naphthoquinone 
• 5312-97-0 2,5-dimethoxybenzonitrile 
• 897018-33-6 methyl 1-(2,5-dimethoxyphenyl)-8-isopropoxy-9-methoxy-5,6-dihydropyrrolo[2,1-a]isoquinoline-3-carboxylate 
• 905912-26-7 6-(2,5-dimethoxy-phenyl)-2,2,4-trimethyl-1,2-dihydro-quinoline 
• 862168-14-7 4-chloro-6-(2,5-dimethoxy-phenyl)-pyrimidin-2-yl-amine 
• 862113-26-6 2-{2-[2-(2,5-dimethoxy-phenyl)-1H-indol-3-yl]-ethyl}-isoindole-1,3-dione 
• 654075-23-7 ethyl 2',5'-dimethoxy-3,4,5,6-tetrahydro-[1,1'-biphenyl]-2-carboxylate 
• 654075-22-6 2-(2,5-dimethoxy-phenyl)-cyclopent-1-enecarboxylic acid ethyl ester 

Relevant articles and documents

Thermal and microwave hydrolysis of organotrifluoroborates mediated by alumina

Hydrolysis of organotrifluoroborates to the corresponding organoboronic acids is readily achieved under either thermal or microwave conditions in the presence of alumina. The organoboronic acid products are obtained in good to excellent yields with essent

Mo–Catalyzed One-Pot Synthesis of N-Polyheterocycles from Nitroarenes and Glycols with Recycling of the Waste Reduction Byproduct. Substituent-Tuned Photophysical Properties

A catalytic domino reduction–imine formation–intramolecular cyclization–oxidation for the general synthesis of a wide variety of biologically relevant N-polyheterocycles, such as quinoxaline- and quinoline-fused derivatives, and phenanthridines, is reported. A simple, easily available, and environmentally friendly dioxomolybdenum(VI) complex has proven to be a highly efficient and versatile catalyst for transforming a broad range of starting nitroarenes involving several redox processes. Not only is this a sustainable, step-economical as well as air- and moisture-tolerant method, but also it is worth highlighting that the waste byproduct generated in the first step of the sequence is recycled and incorporated in the final target molecule, improving the overall synthetic efficiency. Moreover, selected indoloquinoxalines have been photophysically characterized in cyclohexane and toluene with exceptional fluorescence quantum yields above 0.7 for the alkyl derivatives.

ORGANIC LIGHT EMITTING DIODE FOR HIGH EFFICIENCY

Disclosed herein is an organic light-emitting diode, comprising: a first electrode, a second electrode opposite the first electrode, and a light-emitting layer and an electron-density-controlling layer in that order between the first electrode and the sec