250665-25-9

Basic information

• Product Name: C₁₀H₁₅BO₄
• Synonyms: C₁₀H₁₅BO₄
• CAS NO: 250665-25-9
• Molecular Weight: 210.038
• Mol File: 250665-25-9.mol
• Article Data: 6

Chemical Properties

• CAS DataBase Reference: C₁₀H₁₅BO₄(CAS DataBase Reference)
• NIST Chemistry Reference: C₁₀H₁₅BO₄(250665-25-9)
• EPA Substance Registry System: C₁₀H₁₅BO₄(250665-25-9)

Safety Data

• Hazardous Substances Data: 250665-25-9(Hazardous Substances Data)

Upstream product

• 121-43-7 Trimethyl borate 
• 151-10-0 1,3-Dimethoxybenzene 
• 16932-45-9 1-bromo-2,6-dimethoxybenzene 

Downstream Products

• 23112-96-1 (2,6-dimethoxyphenyl)boronic acid 
• 848409-29-0 [(S)-6-(2,6-Dimethoxy-phenyl)-chroman-3-yl]-dimethyl-amine 
• 124318-70-3 2-(2',6'-Dimethoxyphenyl)-1,10-phenanthroline 
• 124318-69-0 2,9-bis(2,6-dimethoxyphenyl)-3-ethynyl-[1,10]-phenanthroline 
• 500711-47-7 2-chloro-9-(2,6-dimethoxyphenyl)-1,10-phenanthroline 
• 500711-50-2 2-(4-chloromethyl-2,6-dimethoxyphenyl)-9-(2,6-dimethoxyphenyl)-1,10-phenanthroline 
• 500711-49-9 9-(2,6-dimethoxyphenyl)-2-{2,6-dimethoxy-4[(2-tetrahydropyranyloxy)methyl]phenyl}-1,10-phenanthroline 
• 309977-94-4 C₈H₁₀BFO₄ 

Relevant articles and documents

Synthesis of substituted azulenes via Pt(II)-Catalyzed ring-expanding cycloisomerization

Substituted azulenes, valuable structures for electronic devices and pharmaceuticals, have been synthesized by the platinum(II)-catalyzed intramolecular ring-expanding cycloisomerization of 1-en-3-yne with ortho-disubstituted benzene. This novel method provides an alternative route for the efficient synthesis of substituted azulenes. The reaction mechanism of selected catalytic transformations was explored using density functional calculations.

Novel 3-aminochromans as potential pharmacological tools for the serotonin 5-HT7 receptor

The synthesis of novel C6-aryl substituted derivatives of 3-(dimethylamino)chroman is described. The novel derivatives display 5-HT 7 receptor affinities that varies from nM to μM, indicating that this small set of derivatives constitute a nove

A facile route to Aryl-substituted 1,10-phenanthrolines by means of Suzuki coupling reactions between substituted areneboronic acids and halogeno-1,10-phenanthrolines

Twelve new mono- or diaryl-substituted 1,10-phenanthrolines (17 and 18) have been synthesized. The key step is a Suzuki coupling reaction between the substituted areneboronic acids 6, 11, and 15 and the mono- and dihalo-1,10-phenanthrolines 16. The syntheses of bis-ortho-substituted boronic acids 6, 11, and 15 from substituted arenes 5 or substituted bromoarenes 10 and 14 by lithiation and subsequent treatment with trimethyl borate is described. Not only 2,9-diiodo- (16c) but also 2,9-dichloro-1,10-phenanthroline (16b) can be used with good yields (65-92%) in the described Suzuki coupling. For the syntheses of unsymmetrically substituted 1,10-phenanthrolines 18b, 18i, and 18j, the use of 2- chloro-9-iodo-1,10-phenanthroline is not necessary; two different bis-ortho-substituted arene rings can be introduced stepwise in 46 to 64% total yield. ( Wiley-VCH Verlag GmbH, 69451 Weinheim, Germany, 2002).