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Naphthylphthalimide

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Identification
Molecular formula
C18H13NO3
CAS number
22342-81-0
IUPAC name
2-(1-naphthylcarbamoyl)benzoic acid
State
State

At room temperature, 2-(1-naphthylcarbamoyl)benzoic acid is in a solid state, often appearing in a crystalline form.

Melting point (Celsius)
222.00
Melting point (Kelvin)
495.15
Boiling point (Celsius)
410.00
Boiling point (Kelvin)
683.15
General information
Molecular weight
293.31g/mol
Molar mass
293.3110g/mol
Density
1.3200g/cm3
Appearence

2-(1-Naphthylcarbamoyl)benzoic acid typically appears as a white crystalline powder. It may vary slightly in form depending on its specific synthesis and purity level.

Comment on solubility

Solubility of 2-(1-naphthylcarbamoyl)benzoic acid

The solubility of 2-(1-naphthylcarbamoyl)benzoic acid can be influenced by several factors, including temperature, polarity, and the presence of various solvents. Understanding its solubility characteristics is essential for its application in both laboratory and industrial settings. Key points to consider include:

  • Solvent Interaction: This compound exhibits varying solubility in different solvents. It is often more soluble in organic solvents like chloroform and ethanol when compared to water.
  • Temperature Effects: As is commonly observed with many organic acids, increasing the temperature generally enhances solubility.
  • Polarity Considerations: The presence of both hydrophobic (naphthyl group) and hydrophilic (carboxylic acid group) moieties leads to complex solubility behavior. The overall polarity dictates its solubility in specific environments.

In conclusion, the solubility of 2-(1-naphthylcarbamoyl)benzoic acid is a nuanced aspect that plays a crucial role in its utility and reactivity in different chemical processes. Understanding these principles can help chemists tailor their experiments effectively.

Interesting facts

Interesting Facts about 2-(1-naphthylcarbamoyl)benzoic Acid

2-(1-naphthylcarbamoyl)benzoic acid, often abbreviated as NCB, is a fascinating compound with unique properties and applications in the field of organic chemistry. Here are some intriguing aspects of this compound:

  • Structural Complexity: The compound features a complex structure that includes both a naphthalene and a benzoic acid moiety. This combination allows for various **intramolecular interactions**, such as hydrogen bonding.
  • Potential Applications: 2-(1-naphthylcarbamoyl)benzoic acid has been explored for its role as a **pharmaceutical intermediate**. Its structure makes it a candidate for developing drugs targeting specific biological activities.
  • Crystallization Studies: Scientists are particularly interested in the crystallization behavior of this compound due to its potential to form interesting **polymorphs**. Each polymorph can exhibit distinct physical properties.
  • UV-Vis Spectroscopy: The compound displays UV absorption, making it useful in photochemical studies. Its ability to absorb light in the UV spectrum opens doors for various **spectroscopic analysis** techniques.
  • Environmental Considerations: In recent years, research has focused on understanding the **environmental impact** of such compounds. The biodegradability and toxicity profiles are essential for assessing their safety.

In summary, 2-(1-naphthylcarbamoyl)benzoic acid is not just another compound; it is a potential key player in organic synthesis and medicinal chemistry. Researchers are excited about its prospects, and as studies progress, we can expect to learn even more about its unique properties and applications.

Synonyms
NAPTALAM
132-66-1
Grelutin
N-(1-Naphthyl)phthalamic acid
N-1-Naphthylphthalamic acid
2-(naphthalen-1-ylcarbamoyl)benzoic acid
Alanap
Alanape
Analape
Dyanap
Peach-Thin
Mor-Cran
Alanap 1
Alanap 3
Naphthalam
Ancrack
Alanap 10G at
Nip-a-thin
1-N-Naphthylphthalamic acid
Naptalame
Cyanap
Naptro
NSC 204421
Alanap Plus
alpha-Naphthylphthalamic acid
N-1-Naphthyl-phthalamidsaeure
Benzoic acid, 2-[(1-naphthalenylamino)carbonyl]-
Alanap 10G
Naftalam
Phthalamic acid, N-1-naphthyl-
Peach Thin 322
ACP 322
Caswell No. 592
N-1-Naphthylphthalamate
N-alpha-Naphthylphthalamic acid
2-[(1-Naphthylamino)carbonyl]benzoic acid
2-((1-Naphthalenylamino)carbonyl)benzoic acid
HSDB 1742
2-(1-Naphthylcarbamoyl)benzoic acid
MFCD00037725
Kyselina N-1-naftylftalamova
EPA Pesticide Chemical Code 030702
6Q8
Naphthylphthalamic acid
AI3-23463
N-(1-naphthalenyl)phthalamic acid
N-1-napthylphthalamic acid
Benzoic acid, 2-((1-naphthalenylamino)carbonyl)-
.alpha.-Naphthylphthalamic acid
2-[(naphthalen-1-yl)carbamoyl]benzoic acid
DTXSID6032437
CHEBI:60833
N-(.alpha.-Naphthyl)phthalamic acid
306R88V86P
NSC-204421
2-[N-(1-naphthylcarbamoyl)]benzoic acid
Naftalam [Czech]
Benzoic acid, 2-((1-naphthalenylamino)carbonyl)- (9CI)
Naptalam [BSI:ISO]
Naptalame [ISO-French]
NPA (VAN)
N-1-Naphthalenephthalamic acid
2-((1-Naphthalenylamino)carbonylbenzoic acid
2-[(1-Naphthalenylamino)carbonylbenzoic acid
N-(1-Naphthyl)phthalamidic acid
Kyselina N-1-naftylftalamova [Czech]
BRN 2814102
N-1-Naphthyl-phthalamidsaeure [German]
Benzoic acid, 2-[(1-naphthalenylamino)carbonyl]- (9CI)
N-1-Naphthylphthalamidic acid
UNII-306R88V86P
C18H13NO3
E7O
Solo (Salt/Mix)
NAPTALAM [HSDB]
NAPTALAM [ISO]
NAPTALAM [MI]
1-Naphthylphthalamic acid
Premerge plus (Salt/Mix)
Oprea1_065903
Oprea1_469302
SCHEMBL54940
CBDivE_002040
3-12-00-02876 (Beilstein Handbook Reference)
WLN: L66J BMVR BVQ
Phthalamic acid, N-1-naphthyl
Phthalamic acid,N-1-naphthyl-
[3H]-NPA
1-(N-Naphthyl)Phthalamic acid
IFLab1_001003
CHEMBL2447888
DTXCID4012437
BDBM81777
JXTHEWSKYLZVJC-UHFFFAOYSA-
NPA,(-)
N-.alpha.-Naphthylphthalamic acid
HMS1414N13
NSC_8594
Tox21_302279
NSC204421
STK072761
AKOS000485934
HY-116425R
N-1-Naphthylphthalamic acid (Standard)
NCGC00255281-01
AS-67711
CAS-132-66-1
DA-76297
SY052096
HY-116425
CS-0065451
N0067
Naptalam, PESTANAL(R), analytical standard
NS00000513
Phthalamic acid, N-1-naphthyl- (7CI,8CI)
2-[(1-Naphthylamino)carbonyl]benzoic acid #
C18869
D91636
AE-017/30049056
L001060
SR-01000392378
SR-01000392378-1
Q11751616
F0290-1094
InChI=1/C18H13NO3/c20-17(14-9-3-4-10-15(14)18(21)22)19-16-11-5-7-12-6-1-2-8-13(12)16/h1-11H,(H,19,20)(H,21,22)