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About This Item
Linear Formula:
C2H5OC6H4CONH2
CAS Number:
Molecular Weight:
165.19
NACRES:
NA.22
PubChem Substance ID:
UNSPSC Code:
12352100
EC Number:
213-346-4
MDL number:
Assay:
97%
Product Name
2-Ethoxybenzamide, 97%
InChI key
SBNKFTQSBPKMBZ-UHFFFAOYSA-N
InChI
1S/C9H11NO2/c1-2-12-8-6-4-3-5-7(8)9(10)11/h3-6H,2H2,1H3,(H2,10,11)
SMILES string
CCOc1ccccc1C(N)=O
assay
97%
mp
132-134 °C (lit.)
Quality Level
Related Categories
Storage Class
11 - Combustible Solids
wgk
WGK 2
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Eyeshields, Gloves, type N95 (US)
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Yoshihiro Hayashi et al.
Pharmaceutics, 12(7) (2020-07-02)
We previously reported a novel method for the precise prediction of tablet properties (e.g., tensile strength (TS)) using a small number of experimental data. The key technique of this method is to compensate for the lack of experimental data by
N Hirasawa et al.
Chemical & pharmaceutical bulletin, 47(3), 417-420 (1999-04-23)
Solid dispersions of carbamazepine or ethenzamide were prepared by melting and rapid cooling with liquid nitrogen using lactose as a carrier. The physical characteristics of these solid dispersions were investigated by powder X-ray diffraction, differential scanning calorimetry, and dissolution rate
Y Miyamoto et al.
Chemical & pharmaceutical bulletin, 46(9), 1432-1437 (1998-10-17)
A computer optimization technique based on surface response methodology was applied to optimize the wet granulation process for designing tablets. Physical properties (mean granule size, granule size distribution, compressibility, granule strength) of a model granule formulation containing ethenzamide were accurately
H Uehara et al.
Cancer letters, 135(1), 83-90 (1999-03-17)
Six-week-old male F344 rats were given a mixture of 0.01% diethylnitrosamine, 0.05% N-butyl-N-(4-hydroxybutyl)nitrosamine and 0.02% N-methyl-N'-nitro-N-nitrosoguanidine in their drinking water for 1 week. When 0.8%, 0.4%, or 0% of a mixture of non-steroidal anti-inflammatory drugs (NSAIDs) (acetaminophen, aspirin, dipyrone plus
Tadashi Fukunaka et al.
Journal of pharmaceutical sciences, 94(5), 1004-1012 (2005-03-29)
Milling is a common procedure to improve bioavailability of many active pharmaceutical ingredients (APIs), which typically have low solubility in water. But such micronization can yield an increase in the cohesiveness of particles. Although particle cohesiveness is desirable for tablet
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