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2-[(3-hydroxy-4-nitro-phenyl)methylene]propanedinitrile

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Identification
Molecular formula
C10H5N3O3
CAS number
962-58-3
IUPAC name
2-[(3-hydroxy-4-nitro-phenyl)methylene]propanedinitrile
State
State

The compound is a solid at room temperature. It is generally stored in its solid form under appropriate conditions to maintain its stability and prevent any moisture uptake which may affect its properties.

Melting point (Celsius)
211.00
Melting point (Kelvin)
484.15
Boiling point (Celsius)
320.00
Boiling point (Kelvin)
593.15
General information
Molecular weight
226.16g/mol
Molar mass
226.1840g/mol
Density
1.3600g/cm3
Appearence

2-[(3-Hydroxy-4-nitro-phenyl)methylene]propanedinitrile appears as an orange to yellow crystalline solid. The compound's coloration is influenced by the nitro and phenolic groups present in its structure.

Comment on solubility

Solubility of 2-[(3-hydroxy-4-nitro-phenyl)methylene]propanedinitrile

The solubility of 2-[(3-hydroxy-4-nitro-phenyl)methylene]propanedinitrile (C10H5N3O3) can be a crucial aspect to understand its behavior in various chemical environments. This compound presents some interesting characteristics, particularly regarding its solubility properties:

  • Polar Nature: The presence of the hydroxyl group (-OH) and nitro group (-NO2) in the molecular structure increases the polarity of the compound, enhancing its solubility in polar solvents.
  • Solvent Compatibility: It is highly soluble in ethanol and water, but shows limited solubility in non-polar solvents like hexane or chloroform.
  • Hydrogen Bonding: The ability to form hydrogen bonds with surrounding molecules can significantly increase solubility in polar solvents.

In conclusion, 2-[(3-hydroxy-4-nitro-phenyl)methylene]propanedinitrile exhibits varying degrees of solubility depending on the solvent system employed. Understanding this aspect is essential for its application in various chemical processes and formulations.

Interesting facts

Interesting Facts about 2-[(3-hydroxy-4-nitro-phenyl)methylene]propanedinitrile

This compound, known as 2-[(3-hydroxy-4-nitro-phenyl)methylene]propanedinitrile, is intriguing due to both its structure and its potential applications in various fields of chemistry. Here are some interesting facts:

  • Chemical Structure: The compound features a distinctive 3-hydroxy-4-nitrophenyl group, which plays a significant role in its reactivity and performance.
  • Biological Relevance: Many compounds that include nitro and hydroxyl groups are studied for their potential biological activities, including anti-cancer and anti-inflammatory properties.
  • Synthesis: The synthesis of this compound often involves approaches that showcase advanced organic chemistry techniques, making it a great example for students learning about compound derivation.
  • Applications: Due to its unique properties, this compound may find usage in organic synthesis, materials science, and possibly in pharmaceutical applications.
  • Color and Stability: Compounds with nitro functional groups often present vibrant color changes upon exposure to light or heat, presenting an avenue for research in photochemistry.

In conclusion, 2-[(3-hydroxy-4-nitro-phenyl)methylene]propanedinitrile is more than just a chemical formula; it's a gateway to exploring complex interactions within organic and medicinal chemistry. Remember the words of Nobel Prize laureate Linus Pauling: "The best way to have a good idea is to have a lot of ideas." This compound exemplifies the depth and breadth of possibilities in chemical research.

Synonyms
118409-62-4
Tyrphostin AG 126
AG-126
AG 126
ag126
Tyrphostin A 10
alpha-Cyano-(3-hydroxy-4-nitro)cinnamonitrile
Tyrphostin AG126
tyrphostin AG-126
2-[(3-hydroxy-4-nitrophenyl)methylidene]propanedinitrile
Propanedinitrile,2-[(3-hydroxy-4-nitrophenyl)methylene]-
7YA4AMD1JC
2-(3-hydroxy-4-nitrobenzylidene)malononitrile
Propanedinitrile, ((3-hydroxy-4-nitrophenyl)methylene)-
TYRPHOSTIN A-10
Tyrphostin AG127
DTXSID80152117
(3-Hydroxy-4-nitrobenzylidene)malononitrile
PROPANEDINITRILE, 2-((3-HYDROXY-4-NITROPHENYL)METHYLENE)-
AG-127
SR-01000076182
UNII-7YA4AMD1JC
BiomolKI_000026
Lopac-T-9177
BiomolKI2_000034
UPCMLD-DP015
Lopac0_001272
BMK1-D2
BSPBio_001196
KBioGR_000536
KBioSS_000536
CHEMBL77387
AG126;Tyrphostin AG 126
BDBM4326
SCHEMBL1802883
DTXCID3074608
UPCMLD-DP015:001
UPCMLD-DP015:002
CHEBI:94704
KBio2_000536
KBio2_003104
KBio2_005672
KBio3_000971
KBio3_000972
DUQADSPERJRQBW-UHFFFAOYSA-N
Bio2_000438
Bio2_000918
HMS1362L17
HMS1792L17
HMS1990L17
HMS3403L17
HMS3648K20
BCP29141
TEA40962
HSCI1_000134
MFCD00236448
s6596
AKOS037515533
AG-126?
CCG-100630
CS-8032
IDI1_002193
NCGC00016062-01
NCGC00016062-02
NCGC00016062-03
NCGC00016062-04
NCGC00016062-05
NCGC00016062-06
NCGC00016062-07
NCGC00094508-01
NCGC00094508-03
NCGC00094508-04
NCGC00094508-05
NCGC00094508-06
NCGC00094508-07
benzylidenemalononitrile (BMN) deriv. 10
BS-14518
HY-108330
??-Cyano-(3-hydroxy-4-nitro)cinnamonitrile
A3345
EU-0101272
C71582
T 9177
SR-01000076182-1
SR-01000076182-4
AG 126 - CAS 118409-62-4
BRD-K67506692-001-03-8
BRD-K67506692-001-04-6
Q27166506
634-194-9