365245-83-6

Basic information

• Product Name: 2-((MethylaMino)Methyl)phenylboronic acid
• Synonyms: 2-((MethylaMino)Methyl)phenylboronic acid
• CAS NO: 365245-83-6
• Molecular Formula: C₈H₁₂BNO₂
• Molecular Weight: 164.99738
• EINECS: -0
• Product Categories: Boronate Ester;Boronic Acid;Potassium Trifluoroborate
• Mol File: 365245-83-6.mol

Chemical Properties

• Boiling Point: 328.3±44.0 °C(Predicted)
• Appearance: /
• Density: 1.11±0.1 g/cm3(Predicted)
• Storage Temp.: under inert gas (nitrogen or Argon) at 2–8 °C
• PKA: 8.33±0.53(Predicted)
• CAS DataBase Reference: 2-((MethylaMino)Methyl)phenylboronic acid(CAS DataBase Reference)
• NIST Chemistry Reference: 2-((MethylaMino)Methyl)phenylboronic acid(365245-83-6)
• EPA Substance Registry System: 2-((MethylaMino)Methyl)phenylboronic acid(365245-83-6)

Safety Data

• Hazardous Substances Data: 365245-83-6(Hazardous Substances Data)

Usage

Uses

Used in Organic Synthesis:
2-((Methylamino)Methyl)phenylboronic acid is used as a reagent in organic synthesis for the formation of carbon-carbon bonds. Its ability to participate in the Suzuki-Miyaura coupling reaction makes it a valuable component in creating complex organic molecules.
Used in Medicinal Chemistry:
In the field of medicinal chemistry, 2-((Methylamino)Methyl)phenylboronic acid serves as a building block for the synthesis of various pharmaceuticals and biologically active molecules. Its unique structure allows for the development of new compounds with potential therapeutic applications.
Used in Material Development:
2-((Methylamino)Methyl)phenylboronic acid has potential applications in the development of new materials. Its properties can be harnessed to create innovative materials with specific characteristics for various industries.
Used in Biological Research:
2-((MethylaMino)Methyl)phenylboronic acid also serves as a tool for studying biological processes. Researchers can use 2-((Methylamino)Methyl)phenylboronic acid to investigate the interactions of molecules within biological systems, potentially leading to a better understanding of certain biological phenomena.

Upstream product

• 40138-16-7 2-formylbenzene boronic acid 
• 74-89-5 methylamine 
• 103-67-3 benzyl-methyl-amine 

Downstream Products

• 1099599-99-1 O(Cl(OH)C₆HCH₂N(CH₃)CH₂C₆H₄B(OH)2)2CC₆H₄C(O)O 
• 13737-31-0 N-methyl-2-aminomethylbiphenyl 
• 1259394-23-4 2-((N-t-butoxycarbonyl-N-methyl)aminomethyl)phenylboronic acid 
• 1101146-70-6 [2-amino-6-[2-(methylaminomethyl)phenyl]quinazolin-4-yl]isoindolin-2-ylmethanone 

Relevant articles and documents

A sorbitol-selective fluorescence sensor

A new anthracene derivative bearing two phenylboronic acid groups at the 1,8-positions was prepared and its binding properties towards sorbitol, xylitol, fructose, glucose and galactose have been studied using fluorescence analysis.

PHENYLQUINAZOLINE DERIVATIVES

Novel quinazolinamide derivatives of the formula (I), in which R1-R43 and X have the meanings indicated in claim 1, are HSP90 inhibitors and can be used for the preparation of a medicament for the treatment of diseases in which the inhibition, regulation and/or modulation of HSP90 plays a role.

Efficient preparation of 2-aminomethylbiphenyls via suzuki-miyaura reactions

We prepared four 2-(aminomethyl)arylboronic acids and studied their reactivity in the Suzuki-Miyaura coupling reaction with different aryl halides. We observed significant increases in yields and shorter reaction times when the amine adjacent to the boron

MICROORGANISM KILLING COMPOUNDS

Compounds, pharmaceutical compositions, and methods of using either to kill microorganisms are disclosed.