Interesting facts
Interesting Facts about 2-Aminobenzamide
2-Aminobenzamide is an intriguing compound in the realm of organic chemistry, primarily known for its role as a building block in the synthesis of more complex molecules. Here are some noteworthy aspects of this compound:
- Structural Significance: The presence of the –NH₂ (amino) group and the –C(=O) (carbonyl) group make 2-aminobenzamide a vital precursor for the synthesis of pharmaceuticals and agrochemicals.
- Biological Activity: Compounds related to 2-aminobenzamide exhibit a range of biological properties, including potential anti-tumor and anti-inflammatory activities, highlighting its importance in drug discovery.
- Reactivity: This compound is known to engage in various chemical reactions, such as acylation and amidation, allowing chemists to create diverse derivatives tailored for specific functions.
- Polymer Chemistry: 2-Aminobenzamide can also play a role in developing polymers, particularly those used in specialty coatings and films due to its relative stability and reactivity.
The study of 2-aminobenzamide not only aids in the understanding of organic reaction mechanisms but also emphasizes the importance of compounds derived from aromatic structures. As noted by chemists, its “diversity in applications from pharmaceuticals to materials science makes it a compound of great interest.”
Overall, 2-aminobenzamide offers an extensive field of exploration for students and researchers alike, making it a fascinating subject within organic chemistry.
Synonyms
2-AMINOBENZAMIDE
Anthranilamide
88-68-6
Benzamide, 2-amino-
o-Aminobenzamide
Aminobenzamide
2-Carbamoylaniline
Anthranilimidic acid
Anthranilic acid amide
Benzamide, o-amino-
Anthranilamide (VAN)
o-Aminobenzamide (VAN)
2-Amino-Benzamide
2-Aminobenzamide (VAN)
Anthranilimidic acid (VAN)
Benzoic acid, 2-amino-, amide
MFCD00007981
28144-70-9
HSDB 5261
Benzenecarboximidicacid, 2-amino-
Q1M2WEK6VA
EINECS 201-851-2
NSC 38768
ortho-aminobenzamide
Benzamide, o-amino- (VAN)
BRN 0508509
DTXSID2021789
2-Aminobenzimidic acid
AI3-28018
NSC-38768
AMINOBENZAMIDE, 2-
2-Amino-Benzamideanthranilamide
DTXCID501789
2-AMINOBENZAMIDE [HSDB]
4-14-00-01010 (Beilstein Handbook Reference)
UNII-Q1M2WEK6VA
oAminobenzamide
2aminobenzamide
amino-benzamide
2Carbamoylaniline
o-carbamoylaniline
o-amino-benzamide
Benzamide, oamino
2-aminobenz-amide
2-Amino benzamide
Benzamide, 2amino
2AE
2- amino-benzamide
anthranilic acid imine
oAminobenzamide (VAN)
2-amino benzamide, 7
2Aminobenzamide (VAN)
2-aminobenzenecarboxamide
Anthranilamide, >=98%
Benzamide, o-amino-(VAN)
Oprea1_246280
SCHEMBL38228
Benzoic acid, 2amino, amide
MLS001066328
CHEMBL43175
SCHEMBL11068162
BDBM33219
CHEBI:193638
HMS1732D11
HMS2269G08
CS-D1680
NSC38768
STR02027
Benzamide, o-amino-(VAN) (8CI)
Tox21_200412
BBL012278
STL163592
Benzamide, o-amino- (VAN) (8CI)
AKOS000119694
FA34678
PS-5040
CAS-88-68-6
DISCONTINUED. Please see O878507
2-Carbamoylaniline, Anthranilimidic acid
NCGC00247015-01
NCGC00247015-02
NCGC00257966-01
AC-20346
SMR000112353
SY001144
DB-022491
A0262
NS00014945
Anthranilic acid amide;2-Aminobenzamide;2-AB
EN300-17791
A60025
D71115
2-Aminobenzamide 100 microg/mL in Acetonitrile
AT-057/40177776
Q27286892
Z57036632
F3329-0460
Anthranilamide, matrix substance for MALDI-MS, >=99.0% (HPLC)
201-851-2
Solubility of 2-Aminobenzamide
2-Aminobenzamide, with the chemical formula C7H8N2O, demonstrates a notable solubility profile that reflects its polar characteristics. Understanding its solubility can provide insights into its applications and behavior in various environments.
Key Points on Solubility
In summary, the solubility of 2-aminobenzamide is influenced by factors such as solvent type, temperature, and pH. Its capacity to dissolve in various mediums makes it a versatile compound in chemical applications and synthesis.