Interesting facts
Interesting Facts About 2-[2-[(2-hydroxyphenyl)methyleneamino]propyliminomethyl]phenol
This compound, commonly known for its complex organic structure, belongs to the class of substituted phenols. Here are some remarkable insights about this intriguing compound:
- Dual Functionalities: This molecule features both phenolic and imine groups, allowing it to exhibit a variety of chemical behaviors and interactions. Its unique structure makes it particularly interesting for research in medicinal chemistry.
- Potential Biological Applications: Compounds like this one have potential applications in various biological activities. Research suggests they can act as antioxidants, and anti-inflammatory agents, or may even possess anticancer properties.
- Structure-Activity Relationship (SAR): Understanding how the structure of this compound influences its biological activity is crucial. Derived compounds can often lead to the development of more potent and selective drugs.
- Research Focus: Scientists are continually exploring the optimization of similar compounds for increased efficacy and reduced toxicity, making this compound a significant point of interest in synthetic organic chemistry.
- Historical Context: The development of derived phenolic compounds has a rich history in medicinal chemistry, beginning in the early 20th century when scientists first began to unlock the therapeutic potential of phenols.
Overall, 2-[2-[(2-hydroxyphenyl)methyleneamino]propyliminomethyl]phenol stands as an exemplary study subject that showcases the intricate balance between structure and function in chemistry. "Understanding these relationships can lead to groundbreaking advancements in drug design." Its diverse properties and potential applications make it an exciting compound in the ever-evolving field of chemical science.
Synonyms
94-91-7
N,N'-Bis(salicylidene)-1,2-propanediamine
Disalicylalpropylenediimine
Tenamene 60
Cuvan 80
Keromet MD
N,N'-Disalicylidene-1,2-diaminopropane
Copper inhibitor 50
UOP copper deactivator
Carlisle metal deactivator
Du Pont metal deactivator
N,N'-Disalicylidene-1,2-propanediamine
alpha,alpha'-Propylenedinitrilodi-o-cresol
N,N'-Disalicylidene-1,2-propylenediamine
N,N'-Propylenebis(salicylideneimine)
N,N'-Bis(salicylidene)-1,2-diaminopropane
NSC 67004
Metal deactivator 2
N,N'-Disalicyclidene-1,2-propanediamine
MFCD00020104
DMD
N',N-Bis(salicylidene)-1,2-propanediamine
DTXSID2041200
N,2-diaminopropane
N,2-propanediamine
Phenol, 2,2'-((1-methyl-1,2-ethanediyl)bis(nitrilomethylidyne))bis-
NSC-67004
NSC-68420
N,2-propylenediamine
7S023Y0W20
2-{[(1-{[(2-hydroxyphenyl)methylidene]amino}propan-2-yl)imino]methyl}phenol
o-Cresol, .alpha.,.alpha.'-(propylenedinitrilo)di-
2-[2-[(2-hydroxyphenyl)methylideneamino]propyliminomethyl]phenol
N,N'-Propylenebis[salicylideneimine]
Phenol, 2,2'-[(1-methyl-1,2-ethanediyl)bis(nitrilomethylidyne)]bis-
WLN: QR BYUM&Y1&1YUM&R BQ
o-Cresol,.alpha.'-(propylenedinitrilo)di-
.alpha.,.alpha.'-Dipropylenedinitrilodi-o-cresol
EINECS 202-374-2
Salpn ligand
Phenol,2'-[(1-methyl-1,2-ethanediyl)bis(nitrilomethylidyne)]bis-
alpha,alpha'-Dipropylenedinitrilodi-o-cresol
UNII-7S023Y0W20
Keromet MD 80
N,N'-Disalicylal-1,2-propanediamine
SEKURISU AK 24M
alpha,alpha'-(Propylenedinitrilo)di-o-cresol
EC 202-374-2
NCIOpen2_003030
NCIOpen2_003477
.alpha.,.alpha.'-(Propylenedinitrilo)di-o-cresol
ETHANOX 4705
SCHEMBL145541
SCHEMBL339934
SCHEMBL711079
o-CRESOL, alpha,alpha'-(PROPYLENEDINITRILO)DI-
Bis(salicyliden)-propylendiamin
SCHEMBL1270639
SCHEMBL9437414
CHEMBL3185057
DTXCID0021200
RURPJGZXBHYNEM-GDAWTGGTSA-N
N,N'-Disalicylidenepropylenediamine
NSC67004
NSC68420
Tox21_301950
2,2'-[(1-Methyl-1,2-ethanediyl)bis(nitrilomethylidyne)]bis-phenol
AKOS015856192
AKOS037645936
N,N'-Bis(salicylidene)propylenediamine
N,N'-DISALICYLALPROPYLENEDIAMINE
CAS-94-91-7
s12354
NCGC00255509-01
6-[[2-[(6-oxocyclohexa-2,4-dien-1-ylidene)methylamino]propylamino]methylidene]cyclohexa-2,4-dien-1-one
AS-64889
SY234551
DB-057539
N,Na(2)-Disalicylidene-1,2-diaminopropane
CS-0085857
D1307
NS00003066
N,N'-(2-Hydroxybenzylidene)-1,2-propandiamine
N,N'-1,2-PROPYLENEBIS(SALICYLIDENEAMINE)
N,N'-Bis(2-hydroxybenzylidene)-1,2-propanediamine
Q15632721
.alpha.,.alpha.'-(1-Methylethylenediimino)di-ortho-cresol
N,N inverted exclamation mark -Bis(salicylidene)-1,2-propanediamine
2-([(2-([(2-Hydroxyphenyl)methylidene]amino)propyl)imino]methyl)phenol #
2,2'-((1E,1'E)-(Propane-1,2-diylbis(azanylylidene))bis(methanylylidene))diphenol
2-{(E)-[((E)-2-{[(E)-(2-hydroxyphenyl)methylidene]amino}propyl)imino]methyl}phenol
2-((E)-[((e)-2-([(e)-(2-hydroxyphenyl)methylidene]amino)-1-methylethyl)imino]methyl)phenol
257636-52-5
Solubility of 2-[2-[(2-hydroxyphenyl)methyleneamino]propyliminomethyl]phenol
The solubility of 2-[2-[(2-hydroxyphenyl)methyleneamino]propyliminomethyl]phenol in various solvents can be quite nuanced due to its complex structure. Here are some key points regarding its solubility:
As a result, understanding the specific solvent interactions and environmental conditions is crucial for accurately predicting the solubility of this compound. When experimenting with solubility, it should be emphasized that testing in multiple solvents and varying conditions can yield a comprehensive understanding of its behavior in solution.