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Syringaldehyde

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Identification
Molecular formula
C7H6O3
CAS number
134-96-3
IUPAC name
2-[(3,4-dihydroxyphenyl)methylene]propanedinitrile
State
State

At room temperature, syringaldehyde is typically found as a solid.

Melting point (Celsius)
110.00
Melting point (Kelvin)
383.15
Boiling point (Celsius)
332.00
Boiling point (Kelvin)
605.15
General information
Molecular weight
178.17g/mol
Molar mass
178.1690g/mol
Density
1.2500g/cm3
Appearence

Syringaldehyde appears as a yellow to brown crystalline solid. It has a distinctive aromatic odour and its crystals can be observed under appropriate conditions.

Comment on solubility

Solubility of 2-[(3,4-dihydroxyphenyl)methylene]propanedinitrile

The compound 2-[(3,4-dihydroxyphenyl)methylene]propanedinitrile (C7H6O3) exhibits interesting solubility characteristics, influenced by its unique molecular structure containing both nitrile and hydroxyl functional groups.

Solubility Characteristics:

  • Polar Nature: This compound is characterized by a polar molecular structure, which often enhances its solubility in polar solvents.
  • Solvent Compatibility: It is likely to be soluble in water and other polar solvents like ethanol and methanol due to the presence of the hydroxyl (-OH) groups that can form hydrogen bonds.
  • Limited Solubility in Non-Polar Solvents: Conversely, the compound may show low solubility in non-polar solvents such as hexane or toluene, as these solvents do not effectively interact with its polar functional groups.

In summary, the solubility of 2-[(3,4-dihydroxyphenyl)methylene]propanedinitrile is primarily influenced by the polarity of solvents used. As a general rule of thumb in chemistry: "Like dissolves like." Thus, this compound will likely demonstrate greater solubility in solvents with similar polar characteristics.

Interesting facts

Interesting Facts about 2-[(3,4-Dihydroxyphenyl)methylene]propanedinitrile

2-[(3,4-Dihydroxyphenyl)methylene]propanedinitrile is a fascinating compound that showcases the intricate relationship between chemistry and nature. This compound, often associated with various biological and synthetic processes, presents several intriguing aspects:

  • Phenolic Compounds: Its structure features a phenolic group, which is known for its antioxidant properties. This raises questions about potential applications in the pharmaceutical and cosmetic industries where antioxidants are valued.
  • Potential Biological Activity: Compounds similar to this one have been studied for their biological activities, including anti-inflammatory and anti-cancer properties. Research in this area could yield significant medical benefits in tackling various diseases.
  • Synthetic Pathways: The synthesis of this compound can be approached through various chemical reactions, highlighting its versatility in organic synthesis. Understanding the reaction pathways may aid in developing effective synthetic strategies for constructing complex molecules.
  • Research Implications: Scientists exploring food chemistry or herbal medicine may find this compound particularly interesting, as molecules with similar structures are often extracted from naturally occurring sources.

In the words of a renowned chemist, "Chemistry is the study of matter, but I prefer to view it as the study of change." This statement resonates deeply with the study of compounds like 2-[(3,4-dihydroxyphenyl)methylene]propanedinitrile, as its chemical properties hold the potential for impressive changes in various fields.

As research continues, who knows what other unexpected applications this compound may hold? The journey of discovery in the world of chemistry is truly boundless!

Synonyms
Tyrphostin 23
118409-57-7
Tyrphostin A23
AG 18
RG-50810
AG-18
2-(3,4-dihydroxybenzylidene)malononitrile
(3,4-Dihydroxybenzylidene)malononitrile
Tyrphostin AG18
2-[(3,4-dihydroxyphenyl)methylidene]propanedinitrile
Tyrphostin RG50810
Propanedinitrile,2-[(3,4-dihydroxyphenyl)methylene]-
RG 50810
RV0GCD31OJ
AG-18 (Tyrphostin 23)
(3,4-Dihydroxyphenyl)methylene propanedinitrile
C10H6N2O2
MFCD00133899
DTXSID9045215
Propanedinitrile, ((3,4-dihydroxyphenyl)methylene)-
NCGC00016043-03
((3,4-Dihydroxyphenyl)methylene)-Propanedinitrile
2-[(3,4-dihydroxyphenyl)methylene]-propanedinitrile
DTXCID7025215
((3,4-DIHYDROXYPHENYL)METHYLENE)-PROPENEDINITRILE
ag18
CAS-118409-57-7
alpha-Cyano-(3,4-dihydroxy)cinnamonitrile
SR-01000075506
3,4-dihydroxybenzylidenemalononitrile
UNII-RV0GCD31OJ
tyrphostin-23
tyrphostin-AG-18
Tocris-0493
(3,4-dihydroxybenzylidene)propanedinitrile
BiomolKI_000011
Lopac-T-7165
BiomolKI2_000021
cid_2052
Lopac0_001160
Oprea1_072726
AG 18 (Tyrphostin 23)
Tyrphostin 23, >=98%
MLS002153315
CHEMBL76904
SCHEMBL241922
BDBM4339
BMK1-B11
CHEBI:92862
EX-A901
VTJXFTPMFYAJJU-UHFFFAOYSA-N
HMS2233I22
HMS3263H21
HMS3266E18
HMS3369M02
HMS3414G15
HMS3653D19
HMS3678G15
BCP06838
Tox21_110287
Tox21_501160
AG-18?
HSCI1_000108
s8009
STL139213
3,4-Dihydroxybenzylidene malononitrile
AKOS005715658
Tox21_110287_1
AG18;Tyrphostin 23; RG-50810
CCG-100615
CS-1387
FT28633
LP01160
SDCCGSBI-0051127.P002
SDCCGSBI-0051127.P005
3,4-(Dihydroxybenzylidene)malononitrile
NCGC00016043-01
NCGC00016043-02
NCGC00016043-04
NCGC00016043-05
NCGC00016043-06
NCGC00016043-07
NCGC00016043-08
NCGC00016043-17
NCGC00024615-01
NCGC00024615-02
NCGC00024615-03
NCGC00024615-04
NCGC00261845-01
AC-30286
AS-69033
benzylidenemalononitrile (BMN) deriv. 23
HY-15644
SMR001230729
DB-093180
2-(3,4-Dihydroxy-benzylidene)-malononitrile
EU-0101160
SW219523-1
T3503
T 7165
AG 18 - CAS 118409-57-7
SR-01000075506-1
SR-01000075506-3
SR-01000075506-6
BRD-K49657628-001-02-3
BRD-K49657628-001-03-1
BRD-K49657628-001-05-6
BRD-K49657628-001-13-0
BRD-K49657628-001-14-8
BRD-K49657628-001-15-5
Q27164614
Tyrphostin 23;Tyrphostin A23; RG-50810; AG 18
F6782-3631
(3,4-Dihydroxybenzylidene)-malononitrile, RG-50810; AG 18
834-432-3