CAS 719-59-5
:2-Amino-5-chlorobenzophenone
Description:
2-Amino-5-chlorobenzophenone, with the CAS number 719-59-5, is an organic compound that belongs to the class of benzophenones, which are characterized by the presence of two aromatic rings connected by a carbonyl group. This particular compound features an amino group (-NH2) and a chlorine atom (-Cl) substituted on the benzophenone structure, specifically at the 2 and 5 positions, respectively. It typically appears as a solid and is known for its potential applications in various fields, including pharmaceuticals and dye manufacturing. The presence of the amino group contributes to its reactivity, allowing it to participate in various chemical reactions, such as nucleophilic substitutions. Additionally, the chlorine atom can influence the compound's electronic properties and solubility. Safety data indicates that it should be handled with care, as it may pose health risks upon exposure. Overall, 2-Amino-5-chlorobenzophenone is a compound of interest in organic synthesis and materials science due to its unique structural features and functional groups.
Formula:C13H10ClNO
InChI:InChI=1S/C13H10ClNO/c14-10-6-7-12(15)11(8-10)13(16)9-4-2-1-3-5-9/h1-8H,15H2
InChI key:InChIKey=ZUWXHHBROGLWNH-UHFFFAOYSA-N
SMILES:C(=O)(C1=C(N)C=CC(Cl)=C1)C2=CC=CC=C2
Synonyms:- (2-Amino-5-chlorophenyl)phenyl-methanone
- (2-Amino-5-chlorophenyl)phenylmethanone
- 2-Amino-5-chlorbenzophenone
- 2-Amino-5-chloro benzophenone
- 2-Amino-5-chlorobenzylphenone
- 2-Benzoyl-4-chloroaniline
- 5-Chloro-2-aminobenzophenone
- Benzophenone, 2-amino-5-chloro-
- Methanone, (2-amino-5-chlorophenyl)phenyl-
- NSC 84157
- Oxazepam benzophenone
- See more synonyms
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Found 19 products.
2-Amino-5-chlorobenzophenone
CAS:Formula:C13H10ClNOPurity:>98.0%(T)Color and Shape:Light yellow to Yellow to Green powder to crystalMolecular weight:231.682-Amino-5-chlorobenzophenone, 98+%
CAS:<p>It is used in the heterocyclic syntheses based on the reactions of dimethyl acetylenedicarboxylate. This Thermo Scientific Chemicals brand product was originally part of the Alfa Aesar product portfolio. Some documentation and label information may refer to the legacy brand. The original Alfa Aesar </p>Formula:C13H10ClNOPurity:98+%Color and Shape:Yellow, Crystals or powder or crystalline powder or fused solidMolecular weight:231.682-Amino-5-chlorobenzophenone
CAS:<p>Amino-aldehydes, amino-ketones and amino-quinones, other than those containing more than one kind of oxygen function; salts thereof, nesoi</p>Formula:C13H10ClNOColor and Shape:Yellow Crystalline PowderMolecular weight:231.045092-Amino-5-chlorobenzophenone
CAS:Formula:C13H10ClNOPurity:98%Color and Shape:SolidMolecular weight:231.67762-Amino-5-chlorobenzophenone
CAS:<p>2-Amino-5-chlorobenzophenone is used as pharmaceutical intermediates.</p>Formula:C13H10ClNOPurity:99.42%Color and Shape:Yellow Crystalline PowderMolecular weight:231.682'-Amino-5'-chlorobenzophenone
CAS:<p>2'-Amino-5'-chlorobenzophenone</p>Purity:99%Color and Shape:Yellow SolidMolecular weight:231.68g/mol2-Amino-5-chlorobenzophenone
CAS:<p>2-Amino-5-chlorobenzophenone</p>Purity:≥98%Molecular weight:231.68g/mol(2-Amino-5-chlorophenyl)phenylmethanone (Aminochlorobenzophenone)
CAS:Controlled ProductFormula:C13H10ClNOColor and Shape:NeatMolecular weight:231.682-Amino-5-chlorobenzophenone
CAS:Formula:C13H10ClNOPurity:≥ 98.0%Color and Shape:Pale yellow to yellow-green powder or crystalsMolecular weight:231.682-Amino-5-chlorobenzophenone
CAS:Controlled Product<p>Applications A metabolite of Diazepam; but has a much weaker anticonvulsant effect.<br>References Hara, T., et al.: J. Med. Chem., 21, 263 (1978),<br></p>Formula:C13H10ClNOColor and Shape:YellowMolecular weight:231.682-Amino-5-chlorobenzophenone
CAS:<p>2-Amino-5-chlorobenzophenone is an ecologically friendly crosslinking agent. It can be used in pharmaceutical preparations, including urine samples for the detection of urochrome and other metabolites. 2-Amino-5-chlorobenzophenone reacts with a phenolic compound via an acylation reaction to form a benzene ring. This reaction is catalyzed by hydrochloric acid and its mechanism is intramolecular hydrogen transfer from the amino group to the carbonyl group that forms a C=N bond. The reaction solution gives off a red color at this stage, which can be detected by optical sensors or by NMR spectroscopy.</p>Formula:C13H10ClNOPurity:Min. 98 Area-%Color and Shape:PowderMolecular weight:231.68 g/mol2-Amino-5-chlorobenzophenone
CAS:Formula:C13H10ClNOPurity:98%Color and Shape:SolidMolecular weight:231.682-Amino-5-Chlorobenzophenone pure, 98%
CAS:Formula:C13H10ClNOPurity:min. 98.0%Color and Shape:Yellow to brown, Crystalline powderMolecular weight:231.68














