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・ N+1
・ N+1 redundancy
・ N,alpha-Diethylphenylethylamine
・ N,N'-Di-2-butyl-1,4-phenylenediamine
N,N'-Di-n-butylthiourea
・ N,N'-diacetylbacillosaminyl-diphospho-undecaprenol alpha-1,3-N-acetylgalactosaminyltransferase
・ N,N'-diacetylchitobiose phosphorylase
・ N,N'-diacetyllegionaminate synthase
・ N,N'-Dicyclohexylcarbodiimide
・ N,N'-Diisopropylcarbodiimide
・ N,N'-Methylenebisacrylamide
・ N,N-Diisopropylaminoethanol
・ N,N-Diisopropylethylamine
・ N,N-Dimethyl-1-naphthylamine
・ N,N-Dimethyldopamine
・ N,N-Dimethylethylamine
・ N,N-dimethylformamidase
・ N,N-Dimethylsphingosine
・ N,N-Dimethyltryptamine


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N,N'-Di-n-butylthiourea : ウィキペディア英語版
N,N'-Di-n-butylthiourea

''N'',''N''′-Di-''n''-butylthiourea is an organic compound with S=C(NH''n''Bu)2 formula. It is thiourea derivative symmetrically substituted with two ''n''-butyl groups on the nitrogen atoms.
==Structure and bonding==

Structure of ''N'',''N''′-Di-''n''-butylthiourea was first determined in 2011. Molecules of this compound exhibit ''syn''-''anti'' conformation. Thiourea core is flat due to high delocalization of electron density. Extended network of N−H⋅⋅⋅S hydrogen bonds is present in this structure. Thiocarbonyl C=S bond distance is equal to 1.712(2) Å, while C−N distances are in range of 1.33 to 1.46 Å.

抄文引用元・出典: フリー百科事典『 ウィキペディア(Wikipedia)
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