CAS 57728-59-3
:N-(3-Chlorobenzoyl)glycine
Description:
N-(3-Chlorobenzoyl)glycine, with the CAS number 57728-59-3, is an organic compound characterized by its structure, which includes a glycine moiety linked to a 3-chlorobenzoyl group. This compound typically appears as a white to off-white crystalline solid. It is soluble in polar solvents such as water and methanol, reflecting its polar functional groups. The presence of the chlorobenzoyl group imparts certain chemical reactivity, making it useful in various synthetic applications, including pharmaceuticals and agrochemicals. The compound may exhibit biological activity, potentially acting as an intermediate in the synthesis of more complex molecules. Its melting point and boiling point can vary based on purity and environmental conditions. As with many chemical substances, handling should be done with care, following appropriate safety protocols to mitigate any risks associated with its use. Overall, N-(3-Chlorobenzoyl)glycine serves as a valuable compound in organic synthesis and research.
Formula:C9H8ClNO3
InChI:InChI=1S/C9H8ClNO3/c10-7-3-1-2-6(4-7)9(14)11-5-8(12)13/h1-4H,5H2,(H,11,14)(H,12,13)
InChI key:InChIKey=ICYUIIJXZHPESK-UHFFFAOYSA-N
SMILES:C(NCC(O)=O)(=O)C1=CC(Cl)=CC=C1
Synonyms:- (3-Chlorobenzoylamino)acetic acid
- 2-[(3-Chlorobenzoyl)amino]acetic acid
- 2-[(3-Chlorophenyl)formamido]acetic acid
- Glycine, N-(3-chlorobenzoyl)-
- Hippuric acid, m-chloro-
- M-Chlorohippurate
- N-(3-Chlorobenzoyl)glycine
- NSC 201882
- m-Chlorohippuric acid
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Found 7 products.
(3-Chloro-benzoylamino)-acetic acid
CAS:Formula:C9H8ClNO3Purity:%Color and Shape:SolidMolecular weight:213.6177[(3-Chlorobenzoyl)amino]acetic acid
CAS:[(3-Chlorobenzoyl)amino]acetic acidPurity:95%Molecular weight:213.62g/molm-Chloro Hippuric Acid
CAS:Controlled Product<p>Applications m-Chlorohippuric Acid is an N-benzoyl derivative with anticonvulsant and cardiotonic activity. m-Chlorohippuric Acid is a metabolite of Isoprophenamine and Ticlopidine (T438325).<br>References Kazaryan, S.A. et al.: Pharm. Chem. J., 35, 485 (2001); Tuong, A. et al.: Eur. J. Drug Metab. Pharmacokin., 6, 91 (1981); Tatsumi, K. et al.: Chem. Pharmac. Bull., 18, 1254 (1970);<br></p>Formula:C9H8ClNO3Color and Shape:NeatMolecular weight:213.62(3-Chloro-benzoylamino)-acetic acid
CAS:Formula:C9H8ClNO3Purity:98%Color and Shape:SolidMolecular weight:213.62m-Chloro Hippuric Acid-d2,15N
CAS:Controlled Product<p>Applications Isotope labelled m-Chlorohippuric Acid is an N-benzoyl derivative with anticonvulsant and cardiotonic activity. m-Chlorohippuric Acid is a metabolite of Isoprophenamine and Ticlopidine (T438325).<br>References Kazaryan, S.A. et al.: Pharm. Chem. J., 35, 485 (2001); Tuong, A. et al.: Eur. J. Drug Metab. Pharmacokin., 6, 91 (1981); Tatsumi, K. et al.: Chem. Pharmac. Bull., 18, 1254 (1970);<br></p>Formula:C9D2H6Cl15NO3Color and Shape:NeatMolecular weight:216.6243-Chlorohippuric acid
CAS:<p>3-Chlorohippuric acid is a drug that inhibits the activity of human liver and pancreatic lipase. This compound has been shown to reduce oxidative injury in animal models. 3-Chlorohippuric acid is also used as an antidiabetic agent, which may be due to its ability to inhibit transcriptional regulation in the pancreas. 3-Chlorohippuric acid binds to siderophores, which are iron-binding molecules present in bacteria. The uptake of this drug into bacteria is mediated by siderophores and may be one mechanism for the bactericidal effect of 3-chlorohippurate.</p>Formula:C9H8ClNO3Purity:Min. 95%Molecular weight:213.62 g/mol






