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化驗
99%
形狀
solid
mp
93-95 °C (lit.)
SMILES 字串
CNc1ccc(Cl)cc1C(=O)c2ccccc2
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
InChI 密鑰
WPNMLCMTDCANOZ-UHFFFAOYSA-N
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應用
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.
訊號詞
Warning
危險聲明
危險分類
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
標靶器官
Respiratory system
儲存類別代碼
11 - Combustible Solids
水污染物質分類(WGK)
WGK 3
閃點(°F)
Not applicable
閃點(°C)
Not applicable
個人防護裝備
dust mask type N95 (US), Eyeshields, Gloves
其他客户在看
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
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
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
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
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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