805572
4-methyl-N-(2-phenylethynyl)-N-(phenylmethyl)-benzenesulfonamide
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经验公式（希尔记法）:
C22H19NO2S
化学文摘社编号:
分子量:
361.46
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22
SMILES string
O=S(N(CC1=CC=CC=C1)C#CC2=CC=CC=C2)(C3=CC=C(C)C=C3)=O
InChI
1S/C22H19NO2S/c1-19-12-14-22(15-13-19)26(24,25)23(18-21-10-6-3-7-11-21)17-16-20-8-4-2-5-9-20/h2-15H,18H2,1H3
InChI key
GVJPCYQNQCNEAO-UHFFFAOYSA-N
form
solid
functional group
phenyl
sulfonamide
storage temp.
2-8°C
Application
Nitrogen-substituted alkynes are strongly polarized alkynes and highly reactive building blocks which have been used for the design of a wide number of transformations. Precursor of highly reactive keteniminium ions and useful reagent for asymmetric synthesis.
存储类别
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
法规信息
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相关内容
Evano group focuses on natural product synthesis, copper catalysis, and hetero-substituted alkynes, emphasizing ynamides' synthetic potential and reactivity.
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