Interesting facts
Interesting Facts about N,N-bis(2-chloroethyl)aniline
N,N-bis(2-chloroethyl)aniline is a fascinating compound with a variety of applications and characteristics that make it intriguing to chemists and researchers alike. Below are some noteworthy aspects of this compound:
- Structure and Function: This compound features a unique molecular structure that includes an aniline base linked by two 2-chloroethyl groups. This configuration enhances its chemical reactivity, making it useful in various syntheses and industrial applications.
- Biological Activity: It is known for its potential biological effects, particularly in the field of medicinal chemistry. Compounds with similar structures have been studied for their pharmacological properties, hinting that N,N-bis(2-chloroethyl)aniline may exhibit similar activities.
- Industrial Uses: This compound can be employed in the production of dyes and pigments. The aniline moiety allows for the synthesis of various dye intermediates, contributing to its value in dye manufacturing.
- Toxicity Considerations: As a chemical with chlorinated alkyl groups, it is important to note that N,N-bis(2-chloroethyl)aniline may exhibit toxic properties. Researchers must handle it carefully and consider environmental impacts when utilizing this compound.
- Historical Significance: The study of compounds containing aniline derivatives dates back to the 19th century, marking an important chapter in the development of organic chemistry. This compound, while less well-known, contributes to the rich tapestry of chemical research evolving from this era.
As you explore the world of N,N-bis(2-chloroethyl)aniline, it's clear that this compound is more than just a chemical formula; it represents a blend of structure, function, and application that provides both challenges and opportunities for chemists.
Synonyms
N,N-Bis(2-chloroethyl)aniline
Aniline mustard
Lymphochin
Lymphocin
Lymphoquin
Benzenamine, N,N-bis(2-chloroethyl)-
Phenylbis(2-chloroethylamine)
N,N,-Di(2-chloroethyl)aniline
UNII-CUJ6745Z9J
NCS-18429
BRN 0880463
AI3-31838
ANILINE MUSTARD [MI]
DTXSID30203820
4-12-00-00253 (Beilstein Handbook Reference)
NSC18429
N,N-BIS(2'-CHLOROETHYL)ANILINE
phenylbis[2-chloroethylamine]
Mustard, Aniline
N,N-bis-(2-chloroethyl)aniline
N, N-Bis(2-chloroethyl)aniline
DTXCID60126311
beta, beta'-dichlorodiethylaniline
Benzenamine, N, N-bis(2-chloroethyl)-
Benzenamine, N,N-bis(2-chloroethyl)-(9CI)
Benzenamine, N, N-bis(2-chloroethyl)-(9CI)
rosjkfflixttaw-uhfffaoysa-n
553-27-5
Mesylerythrol
Lymphoquine
Lymphchin
Anilinlost
N,N-Di(2-chloroethyl)aniline
ANILINE, N,N-BIS(2-CHLOROETHYL)-
NSC-18429
SK 592
TL 476
CB 1074
N,N-Bis(2-chloroethyl)benzenamine
A 14489
MFCD00013689
.beta.,.beta.'-Dichlorodiethylaniline
CUJ6745Z9J
N,N-bis(2-chloroethyl)-N-phenylamine
Anilinlost [German]
NN-Bis(2-chloroethyl)aniline
beta,beta'-Dichlorodiethylaniline
WLN: G2NR&2G
CHEMBL19336
SCHEMBL121635
N,N-bis(2-chloroethyl) aniline
N,N-DI-B-CHLOROETHYLANILINE
N,N-Bis(2-chloroethyl)-benzenamine
AKOS016003020
SB78920
NCGC00186318-01
AS-75665
SY317373
DB-080956
HY-121713
CS-0083103
O12001
AE-641/02429030
Q27275806
Solubility of N,N-bis(2-chloroethyl)aniline
N,N-bis(2-chloroethyl)aniline, with its unique chemical structure, exhibits distinct solubility characteristics. Generally, this compound is characterized as being slightly soluble in water, while showing much greater solubility in organic solvents. Here are some key points about its solubility:
It is important to note that the solubility behavior of N,N-bis(2-chloroethyl)aniline can be influenced by the choice of solvent, temperature, and overall environmental conditions. Understanding these factors is crucial for its practical applications in laboratory and industrial settings.