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2-diphenylboranyloxyethanamine

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Identification
Molecular formula
C14H16BNO
CAS number
374572-76-8
IUPAC name
2-diphenylboranyloxyethanamine
State
State

At room temperature, 2-diphenylboranyloxyethanamine exists in a solid state. The solid is stable under normal conditions of storage.

Melting point (Celsius)
80.00
Melting point (Kelvin)
353.15
Boiling point (Celsius)
250.00
Boiling point (Kelvin)
523.15
General information
Molecular weight
241.13g/mol
Molar mass
241.1300g/mol
Density
1.0100g/cm3
Appearence

2-diphenylboranyloxyethanamine typically appears as a white to off-white solid. Its solid state is characterized by a relatively crystalline structure, and it usually comes in a powdered form. The compound has distinct aromatic properties due to its phenyl groups.

Comment on solubility

Solubility of 2-diphenylboranyloxyethanamine (C14H16BNO)

2-diphenylboranyloxyethanamine demonstrates intriguing solubility characteristics that can be highlighted through several key aspects:

  • Solvent Compatibility: This compound is generally soluble in polar aprotic solvents such as dimethyl sulfoxide (DMSO) and acetonitrile. It may also show some solubility in alcohols.
  • Behavior in Water: The solubility of 2-diphenylboranyloxyethanamine in water is expected to be limited. This can be attributed to its bulky phenylic groups that hinder the interaction with water molecules.
  • Structural Influence: The presence of the boron atom in its structure is noted to enhance interactions in organic solvents, promoting greater solubility through possible coordination complexes.
  • Temperature Effects: Like many organic compounds, its solubility may improve with increasing temperature. A higher thermal energy often facilitates the disruption of intermolecular interactions.

In summary, the solubility of 2-diphenylboranyloxyethanamine is significantly influenced by its structural components and the type of solvent used. Factors such as polarity and temperature play crucial roles in determining how this compound behaves in various environments.

Interesting facts

Interesting Facts About 2-Diphenylboranyloxyethanamine

2-Diphenylboranyloxyethanamine, a fascinating compound in the field of organic chemistry, presents unique properties and potential applications. Here are some engaging insights about this compound:

  • Dual Functionality: This compound features a boron atom, which is known for its ability to act as a Lewis acid. In organic synthesis, it can serve as a *reactive intermediate*, facilitating various chemical reactions.
  • Applications in Materials Science: The incorporation of boron compounds in polymer chemistry has been extensively studied. They can enhance the *thermal stability* and *mechanical properties* of materials, making them highly conducive for advanced applications.
  • Biological Relevance: Certain boranes have shown potential in biological systems, being explored for their roles in *drug delivery* and *therapeutics*. While the specific biological applications of 2-diphenylboranyloxyethanamine are still under investigation, its structure suggests interesting interaction possibilities with biological molecules.
  • Research Utility: Due to its unique chemical structure, this compound serves as a valuable building block in synthetic organic chemistry, particularly in the *design of new pharmaceuticals* and organic materials.
  • Sustainability Perspective: The use of boron compounds has gained attention for developing sustainable chemical processes. They can help minimize the use of hazardous reagents, aligning with green chemistry principles.

As research progresses, the capabilities and implications of 2-diphenylboranyloxyethanamine continue to unfold, making it a compound of interest for both theoretical studies and practical applications.

Synonyms
2-Aminoethyl diphenylborinate
524-95-8
2-APB
(2-Aminoethoxy)diphenylborane
2-Aminoethoxydiphenylborane
2-((Diphenylboryl)oxy)ethanamine
2-Aminoethoxydiphenylborate
2-aminoethoxydiphenyl borate
2-diphenylboranyloxyethanamine
Borinic acid, diphenyl-, 2-aminoethyl ester
aminoethoxydiphenylborane
Borinic acid, o-(2-aminoethyl)diphenyl-
o-(2-Aminoethyl)diphenylborinic acid
Naturstofreagenz A
B-(2-Aminoethoxy)diphenylborane
(2-Aminoethoxy)(diphenyl)borane
EINECS 208-366-5
MFCD00014823
NSC 17107
C14H16BNO
2-(Diphenylboryloxy)Ethanamine
BRN 2942273
bis phenyl(2-aminoethoxy)borate
E4ES684O93
NATURSTOFFREAGENZ A
NSC-17107
Diphenylborinic Acid 2-Aminoethyl Ester
CHEMBL169233
2-di(phenyl)boranyloxyethanamine
DTXSID0040389
C20698
4-16-00-01642 (Beilstein Handbook Reference)
NSC17107
DIPHENYL(2-AMINOETHOXY)BORANE
2-(DIPHENYLBORYLOXY)ETHYLAMINE
(2-AMINOETHYLOXY)DIPHENYLBORANE
2-Aminoethyl Diphenylborinate (2-APB)
J42.786A
ETHANOL, 2-AMINO-, DIPHENYLBORINATE (ESTER)
BORINIC ACID, B,B-DIPHENYL-, 2-AMINOETHYL ESTER
2-APB compound
2-APB cpd
UNII-E4ES684O93
FZ4
Tocris-1224
2Aminoethoxydiphenylborane
2-aminoethoxydephenylborate
2Aminoethyl diphenylborinate
B(2Aminoethoxy)diphenylborane
BSPBio_002506
SCHEMBL341835
SPECTRUM1505120
SPECTRUM1505159
(2Aminoethoxy)(diphenyl)borane
GTPL2433
DTXCID8020389
2-diphenyl-boranyloxy-ethyl-amine
Borinic acid, 2-aminoethyl ester
CHEBI:131184
HMS3267D17
HMS3412A04
HMS3676A04
O(2Aminoethyl)diphenylborinic acid
2-AMINOETHYLDIPHENYL BORONATE
BDBM50278349
Borinic acid, O(2aminoethyl)diphenyl
HB1208
HSCI1_000087
s6657
STL481977
AKOS003404929
CCG-214123
CS-W010440
FA67501
HY-W009724
SB79870
NCGC00025055-01
NCGC00025055-02
NCGC00025055-03
NCGC00025055-04
AS-60844
Borinic acid, diphenyl, 2aminoethyl ester
SY011103
Diphenylboric acid .beta.-aminoethyl ester
DB-102182
D0281
NS00015246
D70920
Borinic acid, diphenyl, 2aminoethyl ester (9CI)
SR-01000597408
Borinic acid, diphenyl-, 2-aminoethyl ester (9CI)
Q4596857
SR-01000597408-1
BRD-K13346085-001-04-7
Z2216892669
2-Aminoethyl diphenylborinate, for TLC derivatization, >=97.0%
Diphenylborinic acid ethanolamine ester;2-Aminoethyldiphenylborinate