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N-benzoylglycine

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Identification
Molecular formula
C9H9NO3
CAS number
434-22-0
IUPAC name
2-benzamidoacetic acid
State
State

At room temperature, N-benzoylglycine exists as a solid.

Melting point (Celsius)
192.00
Melting point (Kelvin)
465.15
Boiling point (Celsius)
334.00
Boiling point (Kelvin)
607.15
General information
Molecular weight
179.17g/mol
Molar mass
179.1730g/mol
Density
1.5400g/cm3
Appearence

N-benzoylglycine is a crystalline solid which is often described as having a white or off-white appearance.

Comment on solubility

Solubility of 2-benzamidoacetic acid

2-benzamidoacetic acid (C9H9NO3), a member of the amino acid family, exhibits notable solubility characteristics that are crucial for its application in various fields, particularly in pharmaceuticals and biochemistry. Here’s what you need to know:

  • Polar Nature: The presence of both polar amide and carboxylic acid functional groups significantly enhances its ability to interact with polar solvents, especially water.
  • Solvent Compatibility: This compound is generally soluble in water, which facilitates its use in aqueous environments and biological systems.
  • pH Influence: The solubility of 2-benzamidoacetic acid can also be dependent on the pH level of the solution, as the ionization of the carboxylic group varies under different pH conditions. Typically, it displays increased solubility at lower pH levels.
  • Temperature Effects: Like many organic compounds, solubility may increase with a rise in temperature, which can be advantageous in laboratory settings.

Overall, the solubility of 2-benzamidoacetic acid is favorable for applications wherein its properties must be utilized in solution. Its effective solubility profile aids in effective drug formulation and delivery systems. Understanding these solubility traits is essential for chemists and researchers working with this compound in any practical applications.

Interesting facts

Interesting Facts about 2-benzamidoacetic acid

2-benzamidoacetic acid is a fascinating compound that possesses a variety of intriguing properties and applications in both the scientific and medicinal fields. Here are some noteworthy aspects:

  • Derivation: This compound can be seen as a hybrid between an amide and an amino acid, making it a valuable substance for studying biological processes.
  • Pharmaceutical Relevance: Due to its structural similarities to amino acids, 2-benzamidoacetic acid can serve as an important component in the design of novel pharmaceuticals.
  • Biological Activity: Research has indicated that compounds similar to 2-benzamidoacetic acid may exhibit anti-inflammatory and analgesic properties, potentially aiding in pain management therapies.
  • Versatile Intermediate: This compound can act as a building block in organic synthesis, opening avenues for creating more complex organic molecules.
  • Potential for Peptide Formation: Its structure makes it a suitable candidate for incorporation into peptide chains, which can be pivotal in the development of biomaterials and drugs.

In the words of eminent chemists, "Understanding the unique characteristics of compounds like 2-benzamidoacetic acid is essential for advancing drug development and organic synthesis." The ongoing research surrounding this compound continues to unveil its potential, making it a subject of interest for many chemists and pharmacologists.

As you delve deeper into the realm of chemical compounds, keep an eye on 2-benzamidoacetic acid for its evolving significance in current scientific studies!

Synonyms
Hippuric acid
495-69-2
2-Benzamidoacetic acid
N-Benzoylglycine
Benzoylglycine
Glycine, N-benzoyl-
Benzamidoacetic acid
Benzoylaminoacetic acid
hippurate
Hippursaeure
Phenylcarbonylaminoacetic acid
Benzamidoessigsaeure
Benzoylaminoessigsaeure
N-Benzoyl-glycin
(benzoylamino)acetic acid
Acetic acid, (benzoylamino)-
Acido ippurico
2-(Phenylformamido)Acetic Acid
Bz-Gly-OH
66407-11-2
Acido ippurico [Italian]
NSC 9982
MFCD00002692
EINECS 207-806-3
UNII-TE0865N2ET
BRN 1073987
TE0865N2ET
DTXSID9046073
CHEBI:18089
AI3-01062
HIPPURICUM ACIDUM
NSC-9982
N-(phenylcarbonyl)glycine
CHEMBL461
DTXCID7026073
4-09-00-00778 (Beilstein Handbook Reference)
NCGC00159486-02
2-benzamidoacetate
Benzoylaminoethanoic acid
ACETIC ACID,BENZAMIDE HIPPURIC ACID
N-BENZOYL(D5) GLYCINE
CAS-495-69-2
2-benzamidoaceticacid
Benzoylglycin
benzoyl glycine
hippuric-acid
Benzamidoacetate
Benzoylglycocoll
METHYLAMINOLEVULINATE HYDROCHLORIDE IMPURITY H (EP IMPURITY)
METHYLAMINOLEVULINATE HYDROCHLORIDE IMPURITY H [EP IMPURITY]
n-benzoyl-glycine
N-benzoyl glycine
Hippuric acid, Na
Hippuric Acid,(S)
(benzoylamino)-Acetate
Hippuric acid, 98%
benzoylamino-acetic acid
2-benzamidoethanoic acid
Phenylcarbonylaminoacetate
Hippuric acid (Standard)
(benzoylamino)-Acetic acid
bmse000408
Cambridge id 5116993
HIPPURIC ACID [MI]
SCHEMBL7486
TimTec1_002805
Oprea1_124422
Oprea1_492747
MLS001074359
BIDD:ER0490
HIPPURICUM ACIDUM [HPUS]
acetic acid, 2-(benzoylamino)-
NSC9982
Hippuric acid, puriss., 99.0%
HMS1541P11
HMS2230I23
HMS3373I07
ALBB-005966
BCP25964
HY-W016562R
Benzenecarboxamide, N-carboxymethyl-
Tox21_111710
BBL008217
BDBM50009999
s5618
STK011394
AKOS000118897
Tox21_111710_1
BS-3968
CCG-266415
CS-W017278
FH23833
HY-W016562
SDCCGMLS-0064636.P001
s11321
NCGC00159486-03
NCGC00159486-04
NCGC00159486-06
SMR000112115
DB-051645
H0143
NS00013745
EN300-16768
C01586
SBI-0633529.0002
AB00375781-06
Q412803
BRD-K62914667-001-13-9
F2111-0036
2-Benzamidoacetic acid;N-Benzoylglycine;Glycine, N-benzoyl-
37C5E4E2-F7A0-451C-A041-5C9A71D92FA7
N-Benzoylglycine;2-(Benzoylamino)acetic acid;2-Benzamidoacetic acid
207-806-3
InChI=1/C9H9NO3/c11-8(12)6-10-9(13)7-4-2-1-3-5-7/h1-5H,6H2,(H,10,13)(H,11,12