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Benzyl Isonicotinate

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Identification
Molecular formula
C13H11NO2
CAS number
94-16-6
IUPAC name
benzyl pyridine-3-carboxylate
State
State

At room temperature, Benzyl Isonicotinate is generally a liquid. It can become more viscous at lower temperatures and should be stored in appropriate conditions to maintain its liquid state.

Melting point (Celsius)
-7.00
Melting point (Kelvin)
266.15
Boiling point (Celsius)
312.00
Boiling point (Kelvin)
585.15
General information
Molecular weight
227.24g/mol
Molar mass
227.2560g/mol
Density
1.1713g/cm3
Appearence

Benzyl Isonicotinate is typically a colorless to pale yellow liquid. It may also appear as a slightly oily consistency depending on its purity and the temperature it is stored at.

Comment on solubility

Solubility of Benzyl Pyridine-3-Carboxylate

Benzyl pyridine-3-carboxylate, known for its intriguing interactions with solvents, exhibits a varied solubility profile that is essential for its applications in chemical processes.

Key points regarding its solubility include:

  • Polar solvents: Benzyl pyridine-3-carboxylate shows moderate solubility in polar solvents such as methanol and ethanol due to its polar functional groups.
  • Non-polar solvents: Conversely, its solubility decreases significantly in non-polar solvents like hexane, highlighting the importance of solvent polarity in determining solubility.
  • Hydrophobic interactions: The compound may exhibit hydrophobic characteristics, which can influence its behavior in aqueous environments, resulting in limited solubility in water.

Therefore, when exploring the solubility of benzyl pyridine-3-carboxylate, it is crucial to consider the solvent environment, as it profoundly affects the compound’s behavior and utility in various applications.

Interesting facts

Interesting Facts about Benzyl Pyridine-3-Carboxylate

Benzyl pyridine-3-carboxylate is a fascinating compound notable for its versatility in organic chemistry. Here are some intriguing aspects of this compound:

  • Structural Diversity: The presence of both a benzyl group and a pyridine ring allows for a rich variety of chemical interactions, making it valuable in the synthesis of other compounds.
  • Pharmaceutical Potential: Compounds containing pyridine rings are often explored for their biological activities, including anti-inflammatory, antimicrobial, and anticancer properties. Benzyl pyridine-3-carboxylate is no exception, warranting further research into its medicinal applications.
  • Examples in Nature: Pyridine derivatives are frequently found in several natural products and can mimic essential biochemical pathways, making them significant in studying metabolic processes.
  • Reaction Pathways: This compound can participate in various organic reactions, such as alkylation and acylation, which are essential for developing complex molecules in drug manufacture and other applications.
  • Research and Development: Scientists are continually exploring this compound's properties, with ongoing studies examining its reactivity, stability, and potential as a building block for more complex chemical structures.

As a compound at the crossroads of synthetic chemistry and medicinal research, benzyl pyridine-3-carboxylate encapsulates the dynamic nature of chemical science. Its myriad potential applications enhance its importance within both academic and industrial settings.

Synonyms
Benzyl nicotinate
94-44-0
Nicotinic acid benzyl ester
Benzyl pyridine-3-carboxylate
Rubriment
Pycaril
Pykaryl
Niacin benzyl ester
3-Pyridinecarboxylic acid, phenylmethyl ester
Benzylis nicotinas
Nicotinsaeurebenzylester
Benzyl nicotinate [JAN]
NICOTINIC ACID, BENZYL ESTER
Pyridin-3-carbonsaeurebenzylester
Benzyl nicotinate (JAN)
Phenylmethyl 3-pyridinecarboxylate
Estru benzylowego kwasu nikotynowego
EINECS 202-332-3
UNII-S497LCF9C9
BRN 0159169
DTXSID7046542
CHEBI:31268
3-pyridinecarboxylic acid phenylmethyl ester
Estru benzylowego kwasu nikotynowego [Polish]
MFCD00023584
S497LCF9C9
DTXCID5026542
KVYGGMBOZFWZBQ-UHFFFAOYSA-
BENZYL NICOTINATE [MART.]
Nicotinic acid, phenylmethyl ester
BENZYL NICOTINATE [WHO-DD]
NCGC00166105-01
NICOTINIC ACID BENZYL ESTER [MI]
BENZYL NICOTINATE (MART.)
Benzylnicotinate
4eh5
Benzyl nicotinate (Standard)
SCHEMBL24600
MLS004773910
CHEMBL209744
BENZYL NICOTINATE [INCI]
HY-B1555R
HMS1716K12
CS-B1730
HY-B1555
Tox21_112318
AKOS001089628
Benzyl nicotinate, >=98.0% (GC)
DS-6445
FB63422
CAS-94-44-0
Pyridine-3-carboxylic acid benzyl ester
NCGC00166105-02
NCGC00166105-03
NCGC00166105-04
AC-13029
DA-61592
SMR001550568
SY033421
N0083
NS00013404
D01419
D77312
SBI-0654043.0001
AB01328141-02
SR-01000940939
Q3876608
SR-01000940939-2
Benzyl Nicotinate, Pharmaceutical Secondary Standard; Certified Reference Material
0OM
202-332-3