Interesting facts
Interesting Facts about Methyl 2-Chloro-5-Nitro-Benzoate
Methyl 2-chloro-5-nitro-benzoate is a fascinating compound with several unique attributes that spark interest within the realm of organic chemistry. Here are some enlightening points about this compound:
- Versatile Intermediate: This compound serves as a key intermediate in the synthesis of various pharmaceuticals and agrochemicals, making it a valuable component in both medicinal chemistry and agricultural applications.
- Functional Group Diversity: Methyl 2-chloro-5-nitro-benzoate exhibits multiple functional groups, including the chloro and nitro substituents. These functionalities can significantly influence the compound's reactivity and properties.
- Electrophilic Reactions: Due to the presence of the electron-withdrawing nitro group, methyl 2-chloro-5-nitro-benzoate is more susceptible to electrophilic substitution reactions, which opens up avenues for further chemical transformations.
- Applications in Synthesis: This compound can be utilized to create more complex molecules through various synthetic routes, such as nucleophilic substitution and coupling reactions, making it highly relevant in research settings.
- Chirality Considerations: The incorporation of a methyl group and the chlorinated site can lead to chiral centers if further transformation occurs, leading to the potential development of enantiomerically pure substances.
- Environmental Perspective: Understanding compounds like methyl 2-chloro-5-nitro-benzoate is essential for evaluating their environmental impact, particularly in terms of degradation pathways and toxicity.
In summary, methyl 2-chloro-5-nitro-benzoate is not just a compound to study but a potential gateway to understanding broader chemical principles and applications. The interplay of functional groups and their effects on reactivity make it a subject of interest in both academic and industrial chemistry.
Synonyms
Methyl 2-chloro-5-nitrobenzoate
6307-82-0
613-139-2
2-Chloro-5-nitrobenzoic acid methyl ester
BENZOIC ACID, 2-CHLORO-5-NITRO-, METHYL ESTER
MFCD00184587
2-chloro-5-nitro-benzoic acid methyl ester
NSC-44287
Methyl 2-chloro-5-nitrobenzenecarboxylate
BRN 1966320
Methyl2-Chloro-5-nitrobenzoate
Methylester kyseliny 2-chlor-5-nitrobenzoove
Methylester kyseliny 2-chlor-5-nitrobenzoove [Czech]
L7RN5S2SA7
4-09-00-01228 (Beilstein Handbook Reference)
SCHEMBL422653
CHEMBL2260451
DTXSID90212397
NSC44287
NSC 44287
STK361847
AKOS000283610
CS-W014889
UPCMLD0ENAT5948501:001
SY007297
2-chloro-1-methoxycarbonyl-5-nitrobenzene
2-Chloro-5-nitrobenzoic acid, methyl ester
DB-054402
C1732
NS00035284
EN300-28646
6W-0299
Q63395371
Z19718166
Solubility of Methyl 2-chloro-5-nitro-benzoate
Methyl 2-chloro-5-nitro-benzoate is a compound with interesting solubility characteristics influenced by its molecular structure. Understanding its solubility can be key for applications ranging from synthesis to formulation.
Solubility Characteristics
In summary, the solubility of methyl 2-chloro-5-nitro-benzoate is driven by its molecular polarity and functional groups. When considering this compound for practical applications, selecting an appropriate solvent can significantly impact its effectiveness.