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N-benzyl-3-chloropropanamide

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Identification
Molecular formula
C10H12ClNO
CAS number
16760-09-1
IUPAC name
N-benzyl-3-chloro-propanamide
State
State

At room temperature, N-benzyl-3-chloropropanamide is in a solid state. It is generally stable under normal ambient conditions and is often handled in laboratory environments in its solid form.

Melting point (Celsius)
64.00
Melting point (Kelvin)
337.15
Boiling point (Celsius)
293.00
Boiling point (Kelvin)
566.15
General information
Molecular weight
197.66g/mol
Molar mass
197.6610g/mol
Density
1.1300g/cm3
Appearence

N-benzyl-3-chloropropanamide appears as a white to off-white crystalline solid. The substance is often found in powdered form and can have a characteristic odor. Its physical state and texture are typical of many crystalline amide compounds.

Comment on solubility

Solubility of N-benzyl-3-chloro-propanamide

N-benzyl-3-chloro-propanamide is an intriguing compound with notable solubility characteristics. Understanding its solubility can help in various applications and reactions. Here are several key points regarding its solubility:

  • Polarity: N-benzyl-3-chloro-propanamide contains both polar and nonpolar regions due to the amide group and the benzyl moiety. This dual nature can lead to variable solubility in different solvents.
  • Solvent Compatibility: This compound is generally more soluble in organic solvents such as ethanol, acetone, and dimethyl sulfoxide (DMSO), rather than in water. The benzyl group contributes hydrophobic characteristics, affecting its interaction with water.
  • Temperature Influence: Like many organic compounds, solubility can increase with temperature. Higher temperatures often enhance the dissolution capacity of N-benzyl-3-chloro-propanamide in organic solvents.

A general rule of thumb in chemistry is that “like dissolves like.” Therefore, compounds that are polar tend to dissolve better in polar solvents, while nonpolar compounds favor nonpolar environments. This principle is crucial for N-benzyl-3-chloro-propanamide when selecting solvents for reactions or extractions.

In summary, N-benzyl-3-chloro-propanamide exhibits solubility primarily in organic solvents owing to its chemical structure. Understanding its solubility profile can aid in efficient laboratory practices and syntheses.

Interesting facts

Interesting Facts about N-benzyl-3-chloro-propanamide

N-benzyl-3-chloro-propanamide is a fascinating compound that belongs to the class of amides, which are derived from carboxylic acids. This compound showcases a unique structure that can lead to intriguing properties and potential applications in various fields.

Key Features:

  • Biological Significance: Compounds like N-benzyl-3-chloro-propanamide are often studied for their potential therapeutic applications. They may exhibit antimicrobial or anticancer properties, making them candidates for drug development.
  • Synthetic Versatility: The presence of both a benzyl group and a chlorine atom allows for intriguing chemical reactivity. This compound can serve as a useful intermediate in synthetic organic chemistry.
  • Pharmaceutical Applications: Due to its unique functional groups, this compound can be used in the design of new pharmaceuticals. Researchers often explore its efficacy in targeting specific biological pathways.
  • Research Opportunities: N-benzyl-3-chloro-propanamide is of interest in the academic community, leading to numerous research studies that aim to better understand its chemical behavior and applications.

As with many nanoscale compounds, researchers emphasize the importance of studying not just the chemical structure but also the behavior of such compounds under various conditions. "The journey of understanding begins with a single compound," a phrase that resonates in the chemistry community, reminding us that every compound holds the potential for discovery.

In summary, N-benzyl-3-chloro-propanamide stands out as a compound with possible implications in medicine, synthetic chemistry, and research, fostering a rich area of study for chemists and students alike. Its intriguing combination of elements opens doors to endless possibilities in scientific exploration.

Synonyms
Beclamide
501-68-8
N-Benzyl-3-chloropropionamide
N-Benzyl-3-chloropropanamide
Neuracen
Chloracon
Chlorakon
Posedrine
Beklamid
Nidrane
Nydrane
Nydran
Seclar
Benzchlorpropamide
Beclamid
Benzylamide
Hibicon
Chloroethylphenamide
Khlorakon
Benzchlorpropamid
Benxchlorpropamide
Benzochlorpropamid
Posedrin
Beclamida
N-(3-Chloropropionyl)benzylamine
Chlorakon (VAN)
Propanamide, 3-chloro-N-(phenylmethyl)-
N-Benzyl-beta-chloropropionamide
Beclamidum
NSC 67062
Beclamidum [INN-Latin]
Beclamida [INN-Spanish]
Beclamide [INN:BAN:DCF]
3-Chloro-N-(phenylmethyl)propanamide
N-Benzyl-beta-chloropropanamide
PROPIONAMIDE, N-BENZYL-3-CHLORO-
UNII-F5N0ALI65V
EINECS 207-927-1
F5N0ALI65V
Beclamide (INN)
NSC-67062
BRN 2720702
DTXSID5057755
N-Benzyl-.beta.-chloropropanamide
N-Benzyl-.beta.-chloropropionamide
BECLAMIDE [INN]
BECLAMIDE [MI]
BECLAMIDE [MART.]
BECLAMIDE [WHO-DD]
DTXCID6031544
4-12-00-02234 (Beilstein Handbook Reference)
Beclamidum (INN-Latin)
Beclamida (INN-Spanish)
BECLAMIDE (MART.)
N03AX30
Propanamide, 3-chloro-N-(phenylmethyl)-(9CI)
207-927-1
jpyqfyieouvjdu-uhfffaoysa-n
N-Benzyl-3-chloro-propionamide
Posedran
Beclamide?
MFCD00018975
WLN: G2VM1R
NCIOpen2_000074
SCHEMBL35199
CHEMBL64195
N-Benzyl-3-chloropropanamide #
SCHEMBL21541521
CHEBI:134859
Pharmakon1600-01505827
N-(Benzyl)-3-Chloro-Propionamide
BCP29693
HY-B1185
NSC67062
Tox21_113912
NSC759264
s5888
STK296069
Beclamide 1.0 mg/ml in Acetonitrile
AKOS000152188
CCG-213990
CS-4794
DB09011
NSC-759264
NCGC00262914-01
AS-36373
CAS-501-68-8
DA-61561
NS00005910
D07300
AB01563371_01
SR-01000944273
Q3637399
SR-01000944273-1
BRD-K44824027-001-01-3
BRD-K44824027-001-02-1