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A45564

Sigma-Aldrich

2-Amino-5-chlorobenzophenone

98%

Synonym(s):

4-Chloro-2-benzoylaniline

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About This Item

Linear Formula:
H2NC6H3(Cl)COC6H5
CAS Number:
719-59-5
Molecular Weight:
231.68
Beilstein/REAXYS Number:
475640
EC Number:
211-949-7
MDL number:
MFCD00007839
UNSPSC Code:
12352100
PubChem Substance ID:
24890879
NACRES:
NA.22

assay

98%

form

powder

mp

96-98 °C (lit.)

SMILES string

Nc1ccc(Cl)cc1C(=O)c2ccccc2

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

ZUWXHHBROGLWNH-UHFFFAOYSA-N

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Related Categories

pictograms

Environment
GHS09

signalword

Warning

hcodes

H410

Hazard Classifications

Aquatic Acute 1 - Aquatic Chronic 1

Storage Class

11 - Combustible Solids

wgk_germany

WGK 3

flash_point_f

388.4 °F - closed cup

flash_point_c

198 °C - closed cup

ppe

dust mask type N95 (US), Eyeshields, Gloves

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F J Rodríguez et al.
Journal of chromatography, 578(1), 146-151 (1992-07-01)
A high-performance liquid chromatographic method with electrochemical detection has been developed for the determination of three aminohalogenbenzophenones: 2-amino-2',5-dichlorobenzophenone, 2-amino-5-chlorobenzophenone and 2-amino-5-bromo-2'-fluorobenzophenone, metabolites of benzodiazepinooxazoles and other psychotropic drugs. A mobile phase of methanol-water (65:35), containing 5 mM KH2PO4 appeared to
R Jain
Journal of chromatography, 615(2), 365-368 (1993-06-02)
A direct densitometric method for determination of diazepam and its metabolites in urine was developed. The proposed procedure involves acid hydrolysis of urine specimens, thereby converting diazepam and its metabolites into benzophenones [2-methylamino-5-chlorobenzophenone (MACB) and 2-amino-5-chlorobenzophenone (ACB)]. It is followed
Swetlana Heinrich et al.
European journal of medicinal chemistry, 46(4), 1331-1342 (2011-02-25)
Previously we described a series of 5-acylaminobenzophenones with considerable antimalarial activity. Unfortunately, most compounds also displayed high cytotoxicity resulting in low selectivity towards malaria parasites. Through the replacement of the 5-acylamino moiety by simple chlorine and further modifications of the

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