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2-methyl-3,5-dinitrobenzamide

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Identification
Molecular formula
C8H7N3O4
CAS number
0
IUPAC name
2-methyl-3,5-dinitro-benzamide
State
State

At room temperature, 2-methyl-3,5-dinitrobenzamide is solid. It is typically handled as a crystalline powder.

Melting point (Celsius)
192.00
Melting point (Kelvin)
465.15
Boiling point (Celsius)
0.00
Boiling point (Kelvin)
0.00
General information
Molecular weight
211.15g/mol
Molar mass
211.1520g/mol
Density
1.4570g/cm3
Appearence

2-Methyl-3,5-dinitrobenzamide typically appears as a yellowish crystalline solid. The compound is characterized by its yellow color, which is consistent with other nitrobenzamides due to the presence of nitro groups.

Comment on solubility

Solubility of 2-methyl-3,5-dinitro-benzamide

2-methyl-3,5-dinitro-benzamide (C8H7N3O4) exhibits interesting solubility characteristics that can be crucial for its applications in various chemical processes. Generally, the solubility of compounds can be influenced by factors such as their molecular structure, the presence of functional groups, and the polarity of the compound itself.

In the case of 2-methyl-3,5-dinitro-benzamide, consider the following points:

  • Polarity: The presence of the nitro groups (-NO2) in this compound increases its polarity, potentially leading to greater solubility in polar solvents, such as water.
  • Hydrogen Bonding: The amide group (-CONH2) can engage in hydrogen bonding, enhancing solubility in polar solvents compared to nonpolar solvents.
  • Solvent Compatibility: While it may exhibit some solubility in water, it is expected to have better solubility in organic solvents like ethanol or acetone due to its hydrophobic aromatic ring.
  • Temperature Effects: Solubility can also vary with temperature, so measuring solubility at different temperatures can provide a more comprehensive understanding of its dissolution behavior.

In summary, while 2-methyl-3,5-dinitro-benzamide might display moderate solubility in polar solvents owing to its functional groups, one must consider the specific solvent characteristics and environmental conditions that may affect its actual solubility. As with many organic compounds, a detailed empirical study is often necessary to ascertain precise solubility values.

Interesting facts

Interesting Facts About 2-Methyl-3,5-Dinitro-Benzamide

2-Methyl-3,5-dinitro-benzamide is an intriguing compound known for its diverse applications in various fields. Here are some fascinating insights into this compound:

  • Structure and Reactivity: The compound features a benzamide backbone, which is further substituted with two nitro groups and a methyl group. This unique structure contributes to its reactivity, especially in electrophilic aromatic substitution reactions.
  • Applications in Research: 2-Methyl-3,5-dinitro-benzamide has gained attention as a reagent in organic synthesis, particularly when exploring new pharmaceuticals and agrochemicals. Its derivatives can exhibit varied biological activities, making it valuable in medicinal chemistry.
  • Explosive Potential: Due to the presence of nitro groups, this compound may also possess explosive characteristics under specific conditions. Nitro-substituted compounds are often studied for their potential use in explosives and propellants, highlighting the importance of safety protocols when handling them.
  • Biological Impact: Some studies have indicated that compounds with similar structures can interact with biological systems, showcasing potential anti-cancer properties. Research is ongoing to understand the mechanisms by which they may influence cellular processes.
  • Environmental Considerations: Like many nitrogen-containing compounds, there can be environmental implications associated with their production and degradation. Understanding how 2-Methyl-3,5-dinitro-benzamide breaks down in nature is essential for assessing its ecological footprint.

In summary, 2-methyl-3,5-dinitro-benzamide is a compound rich in both chemical intrigue and practical applications, representing the fascinating interplay between structure and function in organic chemistry.

Synonyms
dinitolmide
2-Methyl-3,5-dinitrobenzamide
148-01-6
Zoalene
3,5-Dinitro-o-toluamide
Zoamix
Coccidot
Benzamide, 2-methyl-3,5-dinitro-
Coccidine A
Dinitolmida
Dinitrotoluamide
Salcostat
Zoalene [ANSI]
Methyldinitrobenzamide
Dinitolmide [INN:BAN]
Dinitolmidum
Zoalele
Caswell No. 932
Dinitolmidum [INN-Latin]
Dinitolmida [INN-Spanish]
o-Toluamide, 3,5-dinitro-
HSDB 7192
UNII-AOX68RY4TV
EINECS 205-706-4
Dinitolmide (INN)
EPA Pesticide Chemical Code 037510
NSC-758213
BRN 1990738
DTXSID6042521
DINITOLMIDE [MI]
DINITOLMIDE [INN]
AOX68RY4TV
DINITOLMIDE [HSDB]
DINITOLMIDE [MART.]
3,5-Dinitro-ortho-toluamide
ZOALENE [GREEN BOOK]
D.O.T.
DTXCID4022521
3-09-00-02316 (Beilstein Handbook Reference)
Zoalene (ANSI)
NSC 758213
NCGC00094985-01
Dinitolmidum (INN-Latin)
Dinitolmida (INN-Spanish)
DINITOLMIDE (MART.)
C8H7N3O5
Coccidin
3,5-Dinitro Toluamide
Zoalene (500 ug/mL in Methanol)
CAS-148-01-6
SR-01000872611
Abilene
Coccidine
Zamix
3,5-Dinitro-2-methylbenzamide
Whitsyn T
2-methyl-3,5-dinitro-benzamide
ZoaShield 25%
MFCD00072065
3,5Dinitrootoluamide
Dinitolmide (ACGIH)
Dinitolmide (Zoalene)
Spectrum_001272
Dinitolmide, BAN, INN
Spectrum2_000677
Spectrum3_001545
Spectrum4_000732
Spectrum5_001231
2Methyl3,5dinitrobenzamide
SCHEMBL43712
BSPBio_002990
KBioGR_001024
KBioSS_001752
MLS002695903
Benzamide, 2methyl3,5dinitro
DivK1c_000214
SPECTRUM1503036
SPBio_000773
CHEMBL472565
Zoamix Type A Medicated Article
D.O.T. (TN)
HMS500K16
KBio1_000214
KBio2_001752
KBio2_004320
KBio2_006888
KBio3_002490
3,5-Dinitro-o-toluamide, 98%
CHEBI:174162
NINDS_000214
HMS1922A07
HMS3089A22
HMS3652K20
Pharmakon1600-01503036
Zoalene 90 Medicated Coccidiostat
HY-B1004
Tox21_111374
Tox21_301320
BBL003876
CCG-40029
NSC758213
s4141
STK395739
2-Methyl-3,5-dinitrobenzamide, 9CI
AKOS003282656
Tox21_111374_1
CS-4501
DB11480
IDI1_000214
USEPA/OPP Pesticide Code: 037510
NCGC00094985-02
NCGC00094985-03
NCGC00094985-05
NCGC00255914-01
AC-20062
SMR001253784
VS-01441
SBI-0051752.P002
DB-021326
NS00021673
SW219233-1
D07857
E77947
EN300-199771
AB00052301_04
Dinitolmide, VETRANAL(TM), analytical standard
Q4024614
SR-01000872611-2
SR-01000872611-3
BRD-K93240442-001-02-7
BRD-K93240442-001-04-3
BRD-K93240442-001-08-4
Z971222254
205-706-4