Interesting facts
Interesting Facts about N-benzyl-N-(2-chloroethyl)-1-phenoxy-propan-2-amine
N-benzyl-N-(2-chloroethyl)-1-phenoxy-propan-2-amine, often referred to in chemical literature by its more concise name, is a fascinating compound with unique applications and properties. Here are some engaging insights for both students and enthusiasts in the field of chemistry:
- Pharmaceutical Potential: This compound has garnered interest in medicinal chemistry for its possible use as a drug. Its structure suggests that it may interact with various biological targets, making it a candidate for further pharmacological studies.
- Chloride Group Importance: The presence of the chlorine atom in its molecular structure plays a crucial role in enhancing its reactivity and biological activity. Compounds containing halogens often exhibit improved lipophilicity, facilitating cellular absorption.
- Versatile Applications: Due to its phenoxy-propane structure, this compound can be potentially used in numerous industrial applications, ranging from agrochemicals to polymer sciences.
- Structure-Activity Relationship (SAR): Scientists are particularly interested in its molecular framework, which allows for extensive modifications leading to insights into how structural changes can impact biological efficacy and toxicity, which is fundamental in drug design.
- Study of Interactions: The compound can exhibit interesting interactions with receptors or enzymes in biological systems. By understanding these interactions, researchers can develop more effective therapeutic agents or inhibitors.
- Research Opportunities: The exploration of N-benzyl-N-(2-chloroethyl)-1-phenoxy-propan-2-amine offers a wide array of research opportunities, from synthesis and characterization to the study of its mechanism of action within biological systems.
As chemistry students or budding scientists, diving into the world of N-benzyl-N-(2-chloroethyl)-1-phenoxy-propan-2-amine can enhance understanding and spark creativity in various fields, including synthesis and medicinal chemistry. Exploring such compounds allows us to appreciate the intricacies and vast potential of organic chemistry!
Synonyms
phenoxybenzamine
Dibenylin
59-96-1
Bensylyt
Benzylyt
Dibenyline
Dibenzyline
Dibenylene
Fenoxibenzamina
Fenossibenzamina
Bensylyte
Fenossibenzamina [DCIT]
N-benzyl-N-(2-chloroethyl)-1-phenoxypropan-2-amine
Phenoxybenzaminum
Fenoxibenzamina [INN-Spanish]
Phenoxybenzaminum [INN-Latin]
688A
Benzenemethanamine, N-(2-chloroethyl)-N-(1-methyl-2-phenoxyethyl)-
CCRIS 505
NSC 37448
A 688
N-(2-Chloroethyl)-N-(1-methyl-2-phenoxyethyl)benzenemethanamine
HSDB 4005
N-(2-Chloroethyl)-N-(1-methyl-2-phenoxyethyl)benzylamine
2-(N-Benzyl-2-chloroethylamino)-1-phenoxypropane
Benzyl(2-chloroethyl)-(1-methyl-2-phenoxyethyl)amine
EINECS 200-446-8
UNII-0TTZ664R7Z
BRN 2129697
N-Phenoxyisopropyl-N-benzyl-beta-chloroethylamine
0TTZ664R7Z
Benzylamine, N-(2-chloroethyl)-N-(1-methyl-2-phenoxyethyl)-
DTXSID0023458
Phenoxybenzamine (INN)
CHEMBL753
CHEBI:8077
DTXCID803458
59-96-1 (free)
(+/-)-PHENOXYBENZAMINE
4-12-00-02204 (Beilstein Handbook Reference)
benzyl(2-chloroethyl)(1-phenoxypropan-2-yl)amine
NCGC00015121-08
N-Phenoxyisopropyl-N-benzyl-.beta.-chloroethylamine
PHENOXYBENZAMINE [INN]
Fenoxibenzamina (INN-Spanish)
Phenoxybenzaminum (INN-Latin)
Phenoxybenzamine [INN:BAN]
CAS-59-96-1
Spectrum_000378
Prestwick0_000944
Prestwick1_000944
Prestwick2_000944
Prestwick3_000944
Spectrum2_001815
Spectrum4_000769
Spectrum5_001370
SCHEMBL5722
Lopac0_000235
BSPBio_000908
BSPBio_001278
BSPBio_002356
KBioGR_000618
KBioGR_001158
KBioSS_000618
KBioSS_000858
PHENOXYBENZAMINE [MI]
DivK1c_000800
SPBio_001829
SPBio_003067
PHENOXYBENZAMINE [HSDB]
BPBio1_001000
GTPL7268
PHENOXYBENZAMINE [VANDF]
KBio1_000800
KBio2_000618
KBio2_000858
KBio2_003186
KBio2_003426
KBio2_005754
KBio2_005994
KBio3_001095
KBio3_001096
C04AX02
PHENOXYBENZAMINE [WHO-DD]
NINDS_000800
Bio2_000479
Bio2_000959
HMS1362P19
HMS1792P19
HMS1990P19
HMS2089J09
HMS3403P19
HY-B0431
N-(2-chloroethyl)-N-(phenylmethyl)-1-(phenyloxy)propan-2-amine
Tox21_110087
BDBM50017679
AKOS015961144
Tox21_110087_1
CCG-204330
DB00925
SB82886
SDCCGSBI-0050223.P004
IDI1_000800
IDI1_002234
MRF-0000619
NCGC00015121-03
NCGC00015121-04
NCGC00015121-05
NCGC00015121-06
NCGC00015121-07
NCGC00015121-09
NCGC00015121-11
NCGC00015121-12
NCGC00015121-13
NCGC00015121-14
NCGC00015121-16
NCGC00015121-17
NCGC00089748-03
NCGC00089748-04
NCGC00089748-05
NCGC00089748-07
AC-13214
DA-56796
SBI-0050223.P003
AB00053702
CS-0255342
NS00009393
EN300-57590
C07435
D08358
AB00053702-12
AB00053702_13
AB00053702_14
L001197
Q419824
BRD-A67799922-003-26-0
BRD-A67799922-003-27-8
BRD-A67799922-003-28-6
N-Benzyl-N-(2-chloroethyl)-1-phenoxy-2-propanamine #
Benzyl-(2-chloro-ethyl)-(1-methyl-2-phenoxy-ethyl)-amine
N-(2-chloroethyl)-N-(1-methyl-2-phenoxyethyl)-benzenemethanamine
102737-84-8
200-446-8
Solubility of N-benzyl-N-(2-chloroethyl)-1-phenoxy-propan-2-amine (C19H22ClNO)
N-benzyl-N-(2-chloroethyl)-1-phenoxy-propan-2-amine is a compound that exhibits interesting solubility characteristics. When discussing solubility, several factors come into play, particularly for organic compounds:
As a general rule, "like dissolves like." The presence of the phenoxy group suggests that the compound may have some ability to interact with organic solvents effectively while struggling in aqueous environments due to its hydrophobic regions.
In summary, while specific solubility values should be determined experimentally, understanding the functional groups within N-benzyl-N-(2-chloroethyl)-1-phenoxy-propan-2-amine provides insight into its solubility potential in various solvents.