191353

5-Chlor-2-(methylamino)benzophenon

Name: 5-Chlor-2-(methylamino)benzophenon
Brand: ALDRICH
Price: 43.4 EUR

99%

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Über diesen Artikel

Lineare Formel:

CH₃NHC₆H₃(Cl)COC₆H₅

CAS-Nummer:

1022-13-5

Molekulargewicht:

245.70

NACRES:

NA.22

PubChem Substance ID:

24851482

UNSPSC Code:

12352100

EC Number:

213-822-1

MDL number:

MFCD00008284

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Produktname

5-Chlor-2-(methylamino)benzophenon, 99%

InChI key

WPNMLCMTDCANOZ-UHFFFAOYSA-N

InChI

1S/C14H12ClNO/c1-16-13-8-7-11(15)9-12(13)14(17)10-5-3-2-4-6-10/h2-9,16H,1H3

SMILES string

CNc1ccc(Cl)cc1C(=O)c2ccccc2

assay

99%

form

solid

mp

93-95 °C (lit.)

Quality Level

100

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1 of 4

Dieser Artikel	463450	C61801	C60201
Sigma-Aldrich 191353 5-Chlor-2-(methylamino)benzophenon	Sigma-Aldrich 463450 Methyl-4-acetamid-5-chlor-2-methoxybenzoat	Sigma-Aldrich C61801 2-Chlor-5-Nitropyridin	Sigma-Aldrich C60201 5-Chlor-2-Nitrobenzoesäure
assay 99%	assay 99%	assay 99%	assay 99%
Quality Level 100	Quality Level 100	Quality Level 100	Quality Level 100
mp 93-95 °C (lit.)	mp 153-156 °C (lit.)	mp 105-108 °C (lit.)	mp 137-139 °C (lit.)
form solid	form -	form powder	form powder

Application

5-Chloro-2-(methylamino)benzophenone was used in the simultaneous determination of hydrazine and benzylhydrazine in isocarboxazid raw material and tablet formulations by gas chromatography[1].

pictograms

GHS07

signalword

Warning

hcodes

H315,H319,H335

pcodes

P261 - P264 - P271 - P280 - P302 + P352 - P305 + P351 + P338

Hazard Classifications

Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

target_organs

Respiratory system

Lagerklasse

11 - Combustible Solids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

dust mask type N95 (US), Eyeshields, Gloves

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Three-photon absorption and vibrational spectroscopic study of 2-methylamino-5-chlorobenzophenone.

D Sajan et al.

Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy, 106, 253-261 (2013-02-16)

In this paper, the vibrational spectral analysis and three-photon absorption properties of an organic material of 2-methylamino-5-chlorobenzophenone have been reported. The geometry and harmonic vibrational wavenumbers are calculated with the help of B3LYP density functional theory method. The detailed interpretation

Growth and characterization of organic material 2-methylamino-5-chlorobenzophenone single crystal by modified vertical Bridgman technique.

T Suthan et al.

Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy, 79(5), 1443-1448 (2011-05-24)

The organic material 2-methylamino-5-chlorobenzophenone single crystal has been grown by modified vertical Bridgman technique using the single wall ampoule with nano translation. The grown crystal was confirmed by single crystal and powder X-ray diffraction analyses. Fourier transform infrared analysis was

Acid hydrolysis of diazepam. Kinetic study of the reactions of 2-(N-methylamino)-5-chlorobenzophenone, with HCl in MeOH-H2O.

N S Nudelman et al.

Journal of pharmaceutical sciences, 84(8), 998-1004 (1995-08-01)

In the acid hydrolysis of diazepam (1), several unusual products, apart from 2-(N-methylamino)-5-chlorobenzophenone (2) and glycine, were isolated. On the assumption that some of those products could arise from further degradation of 2, the reaction of this compound with 0.5-2

[The preservability of sibazon breakdown products in the cadavers of experimental animals].

M I Krut'

Sudebno-meditsinskaia ekspertiza, 41(3), 24-26 (1998-08-15)

Cibasone degradation products were measured in corpses of 15 cats poisoned with cibasone in a dose of 750 mg/kg. Cibasone was assessed by semiquantitative method on Silufol UV-254 plates from the content of the main degradation product 3-methylamino-5-chloro-benzophenone (MCB) in

Simplified method for simultaneous determination of diazepam and its metabolites in urine by thin-layer chromatography and direct densitometry.

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

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