Interesting facts
Interesting Facts about 1-(Chloromethyl)-2-nitro-benzene
1-(Chloromethyl)-2-nitro-benzene, a valuable organic compound, exhibits fascinating chemical properties and applications in material science and medicinal chemistry. Here are some intriguing aspects of this compound:
- Reactivity: The presence of both a chloromethyl group and a nitro group makes this compound highly reactive, particularly in nucleophilic substitution reactions. This can lead to the formation of various derivatives, enhancing its versatility in chemical synthesis.
- Synthesis Applications: It is often utilized as an intermediate in the synthesis of pharmaceuticals, agrochemicals, and fine chemicals, making it an essential compound in industrial settings.
- Role in Research: Researchers employ this compound to study reaction mechanisms and to explore the reactivity of nitro-substituted aromatic compounds. Its structure allows for investigation into the effects of electronic and steric factors.
- Biological Interest: The nitro group in this compound can undergo reduction in biological systems, which has drawn interest in the context of medicinal chemistry, especially for designing drugs that target specific biological pathways.
- Environmental Considerations: Like many chlorinated compounds, it poses potential environmental and health risks, making safety protocols essential during its handling and application.
As a student or researcher in chemistry, studying 1-(chloromethyl)-2-nitro-benzene not only offers insights into organic synthesis but also provides a gateway to understand the broader implications of such compounds in various fields.
In summary, exploring compounds like 1-(chloromethyl)-2-nitro-benzene can spark curiosity and innovation in chemical research.
Synonyms
2-Nitrobenzyl chloride
612-23-7
O-NITROBENZYL CHLORIDE
alpha-Chloro-2-nitrotoluene
Benzene, 1-(chloromethyl)-2-nitro-
CCRIS 2323
UNII-HB8U484NPM
EINECS 210-300-5
HB8U484NPM
NSC 66500
BRN 0388396
DTXSID9025744
NSC-66500
DTXCID705744
NITROBENZYL CHLORIDE, O-
oNitrobenzyl chloride
2nitrobenzyl chloride
alphaChloroonitrotoluene
alphaChloro2nitrotoluene
Toluene, alphachloroonitro
1(Chloromethyl)2nitrobenzene
Benzene, 1(chloromethyl)2nitro
Benzene, 1(chloromethyl)2nitro (9CI)
Benzene, 1-(chloromethyl)-2-nitro-(9CI)
4-05-00-00854 (beilstein handbook reference)
bxcbuwktxlwpsb-uhfffaoysa-n
inchi=1/c7h6clno2/c8-5-6-3-1-2-4-7(6)9(10)11/h1-4h,5h
un3261
1-(Chloromethyl)-2-nitrobenzene
2-Nitrobenzylchloride
Toluene, .alpha.-chloro-o-nitro-
.alpha.-Chloro-o-nitrotoluene
MFCD00007185
alpha-Chloro-o-nitrotoluene
Toluene, alpha-chloro-o-nitro-
2-nitro-benzylchlorid
1-(Chloromethyl) -2-nitrobenzene;1-(chloromethyl)-2-nitro-benzen
o-Nitrobenzylchlorid
o-nitrobenzylchloride
2-nitro-benzylchloride
SCHEMBL69613
MLS002454429
2-Nitrobenzyl chloride, 99%
CHEMBL175193
1-Nitro-2-(chloromethyl)benzene
1-(Chloromethyl) -2-nitrobenzene
HMS3039H12
NSC66500
Tox21_200821
CK2309
AKOS000294914
NCGC00091732-01
NCGC00091732-02
NCGC00091732-03
NCGC00258375-01
AC-25726
CAS-612-23-7
PS-10632
SMR001372019
DB-000162
N0182
NS00034609
EN300-41224
A24708
A928569
Q27279839
Solubility of 1-(Chloromethyl)-2-nitro-benzene
1-(Chloromethyl)-2-nitro-benzene, with the chemical formula C8H8ClN2O2, exhibits distinct solubility characteristics that might intrigue researchers and chemists alike. Understanding its solubility is crucial for various applications, from synthesis to purification processes.
Solubility Behavior
In terms of solubility, this compound tends to be:
It is crucial to note that the presence of the nitro group in the molecule may enhance its polar characteristics, enabling it to interact with certain polar solvents to a certain extent. As stated in the literature, "Electronegativity and molecular structure play significant roles in determining solubility." Thus, while it is primarily categorized as insoluble in water, certain conditions might still allow for limited interaction with polar solvents.
In summary, the solubility of 1-(chloromethyl)-2-nitro-benzene is a fine blend of its molecular structure and the nature of the solvent used, making further exploration in solubility behavior particularly promising.