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442470

Supelco

Benzanilide

analytical standard

Synonym(s):

N-Benzoylaniline, N-Phenylbenzamide

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About This Item

Linear Formula:
C6H5CONHC6H5
CAS Number:
93-98-1
Molecular Weight:
197.23
Colour Index Number:
42095
Beilstein/REAXYS Number:
1102980
EC Number:
202-292-7
MDL number:
MFCD00003069
UNSPSC Code:
12352200
PubChem Substance ID:
24867863

grade

analytical standard

packaging

ampule of 1000 mg

technique(s)

HPLC: suitable
gas chromatography (GC): suitable

bp

117 °C/10 mmHg (lit.)

mp

161-163 °C (lit.)

application(s)

environmental

format

neat

storage temp.

room temp

SMILES string

O=C(Nc1ccccc1)c2ccccc2

InChI

1S/C13H11NO/c15-13(11-7-3-1-4-8-11)14-12-9-5-2-6-10-12/h1-10H,(H,14,15)

InChI key

ZVSKZLHKADLHSD-UHFFFAOYSA-N

Gene Information

human ... EPHX2(2053)
mouse ... Ephx2(13850)

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Application

Refer to the product′s Certificate of Analysis for more information on a suitable instrument technique. Contact Technical Service for further support.

Storage Class

13 - Non Combustible Solids

wgk_germany

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Gloves, type N95 (US)

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Certificates of Analysis (COA)

Lot/Batch Number
LC20292V
LC17980V
LC17548V
LC16527V
LC11680V

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Joanne V Allen et al.
Bioorganic & medicinal chemistry letters, 21(18), 5224-5229 (2011-08-13)
A directed screen of a relatively small number of compounds, selected for kinase ATP pocket binding potential, yielded a novel series of hit compounds (1). Hit explosion on two binding residues identified compounds 27 and 43 as the best leads
Synthesis of 2-arylbenzoxazoles by copper-catalyzed intramolecular oxidative C-O coupling of benzanilides.
Satoshi Ueda et al.
Angewandte Chemie (International ed. in English), 47(34), 6411-6413 (2008-07-12)
Krzysztof Jóźwiak et al.
Acta poloniae pharmaceutica, 59(5), 341-346 (2003-02-27)
Several groups of 2,4-dihydroxythiobenzanilide derivatives are extensively studied in our laboratories as potential antifungal or antibacterial agents. Previous papers showed that their biological activities are closely correlated with the lipophilicity determined in HPLC experiments using on octadecylsilyl stationary phase (RP-18).
Gerda Brunhofer et al.
Bioorganic & medicinal chemistry, 19(2), 994-1001 (2010-12-28)
A series of dithiobenzanilide derivatives was synthesized and each compound was evaluated for its ability to reduce KCl-induced contractions of smooth muscle preparations of the guinea pig. Starting from a recent publication describing benzanilide derivatives as antispasmodic agents, structure-activity guided
Katherine A Rawls et al.
Bioorganic & medicinal chemistry letters, 19(24), 6851-6854 (2009-11-06)
The development of low muM inhibitors of the Mycobacterium tuberculosis phosphatase PtpA is reported. The most potent of these inhibitors (K(i)=1.4+/-0.3 microM) was found to be selective when tested against a panel of human tyrosine and dual-specificity phosphatases (11-fold vs
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