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

Chemical Properties

white to almost white crystalline powder

Uses

Different sources of media describe the Uses of 107099-99-0 differently. You can refer to the following data:
1. suzuki reaction
2. 2,5-Dimethoxyphenylboronic acid is a bacterial mutagen.

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

Downstream Products

• 478190-83-9 2',5'-bis(4-(N,N-dibutylamino)phenyl)ethynyl-2,2,5,5-tetramethoxy[1,1':4',1]terphenyl 
• 862168-14-7 4-chloro-6-(2,5-dimethoxy-phenyl)-pyrimidin-2-yl-amine 
• 5312-97-0 2,5-dimethoxybenzonitrile 
• 862115-98-8 2-[2-(2,5-dimethoxy-phenyl)-1H-indol-3-yl]-ethylamine 
• 247586-33-0 9,10-bis-(2,5-dimethoxy-phenyl)-anthracene 
• 1159770-80-5 2-(3,6-dioxocyclohexa-1,4-dienyl)-5-methoxy-7-methyl-1,4-naphthoquinone 
• 1228883-11-1 C₂₄H₂₉N₃O₆ 
• 383144-24-9 4-(2,5-dimethoxyphenyl)thiazole-2-carboxaldehyde 
• 1383663-77-1 (Z)-5-(2,5-dimethoxyphenyl)-1-(1,2-diphenylvinyl)-1H-indole 
• 1381870-48-9 2-chloro-4-(2,5-dimethoxyphenyl)pyrido[2,3-d]pyrimidine 
• 1393839-41-2 4-(2,5-dimethoxyphenyl)isoquinoline 

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

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