455725
N,N-Diisopropylbenzamide
98%
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About This Item
Linear Formula:
C6H5CON[CH(CH3)2]2
CAS Number:
Molecular Weight:
205.30
UNSPSC Code:
12352100
PubChem Substance ID:
MDL number:
Assay:
98%
InChI
1S/C13H19NO/c1-10(2)14(11(3)4)13(15)12-8-6-5-7-9-12/h5-11H,1-4H3
SMILES string
CC(C)N(C(C)C)C(=O)c1ccccc1
InChI key
UYXMMJPYFKRKKM-UHFFFAOYSA-N
assay
98%
mp
69-71 °C (lit.)
Storage Class
13 - Non Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
Regulatory Information
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Naphthalene-catalysed lithiation of N,N-diisopropylbenzamide and its methoxy derivatives.
Alonso E, et al.
Tetrahedron, 54(44), 13629-13638 (1998)
2-azaisobenzofurans as intermediates in a convenient annelation of aromatic tertiary amides.
Beak P and Chen C-W.
Tetrahedron Letters, 24(29), 2945-2948 (1983)
Victoria L Blair et al.
Chemistry (Weinheim an der Bergstrasse, Germany), 14(1), 65-72 (2007-11-23)
Extending the recently introduced concept of "alkali-metal-mediated manganation" to functionalised arenes, the heteroleptic sodium manganate reagent [(tmeda)Na(tmp)(R)Mn(tmp)] (1; TMEDA=N,N,N',N'-tetramethylethylenediamine, TMP=2,2,6,6-tetramethylpiperidide, R=CH2SiMe3) has been treated with anisole or N,N-diisopropylbenzamide in a 1:1 stoichiometry in hexane. These reactions afforded the crystalline products
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