693561
(S)-N-(3,5-Dimethylphenyl)-3-methyl-2-(N-formyl-N-methylamino)butanamide
97%
Synonym(s):
Kenamide
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About This Item
Empirical Formula (Hill Notation):
C15H22N2O2
CAS Number:
Molecular Weight:
262.35
MDL number:
UNSPSC Code:
12352002
PubChem Substance ID:
NACRES:
NA.22
assay
97%
form
solid
optical activity
[α]22/D -229°, c = 1 in chloroform
mp
97-104 °C
storage temp.
2-8°C
SMILES string
CC(C)[C@H](N(C)C=O)C(=O)Nc1cc(C)cc(C)c1
InChI
1S/C15H22N2O2/c1-10(2)14(17(5)9-18)15(19)16-13-7-11(3)6-12(4)8-13/h6-10,14H,1-5H3,(H,16,19)/t14-/m0/s1
InChI key
WWUZCRRIJZUXEZ-AWEZNQCLSA-N
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Malkov, A. V.; Stoncius, S.; MacDougall, K. N.; Mariani, A.; McGeoch, G. D.; Kocovsky, P.
Tetrahedron, 62, 264-264 (2006)
Enantioselective synthesis of 1,2-diarylaziridines by the organocatalytic reductive amination of alpha-chloroketones.
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Angewandte Chemie (International ed. in English), 46(20), 3722-3724 (2007-04-07)
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Annals of translational medicine, 9(11), 940-940 (2021-08-06)
Osteoarthritis (OA) is characterized by erosion and degradation of articular cartilage. This study assessed the effects of curcumin on mouse knee cartilage chondrocytes. Chondrocytes were treated for 24 hours with interleukin IL-1β (10 ng/mL) alone, or the combination of curcumin
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Organic letters, 6(13), 2253-2256 (2004-06-18)
[reaction: see text] Asymmetric reduction of ketimines 1 with trichlorosilane can be catalyzed by a new N-methyl L-valine derived Lewis basic organocatalyst, such as 4d, with high enantioselectivity. The structure-reactivity investigation suggests hydrogen bonding and arene-arene interactions between the catalyst
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The Knee, 27(1), 18-25 (2019-12-31)
Articular cartilage is a unique avascular tissue in which chondrocytes are embedded in extracellular matrix (ECM). The decreased ECM resulting from the loss of articular chondrocyte viability leads to degenerative diseases such as osteoarthritis (OA). This study aims to investigate
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