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1)  N methylacetamide
N甲基乙酰胺
2)  N-methylacetamide
N-甲基乙酰胺
1.
Isobaric Vapor-Liquid Equilibria for Water+Acetic Acid+N-methylacetamide;
水-醋酸-N-甲基乙酰胺体系的等压汽液平衡研究
2.
N-Methyl-N-vinylacetamide was synthesized from N-methylacetamide and vinyl acetate with N,N-dimethylamino pyridine (DMAP) as catalyst.
以N-甲基乙酰胺、醋酸乙烯酯为原料,N,N-二甲氨基吡啶(DMAP)为催化剂,合成N-甲基-N-乙烯基乙酰胺。
3.
The ABEEM/MM (atom-bond electronegativity equalization fused into molecular mechanic) fluctuating charge force field was used in molecular dynamic simulation for N-methylacetamide (NMA) aqueous solution.
利用原子键电负性均衡结合分子力场方法(ABEEM/MM)对N-甲基乙酰胺(NMA)分子的水溶液体系进行了分子动力学模拟。
3)  N-vinylformamide
N-乙烯基甲酰胺
1.
The precursor fiber for chelate fiber containing amide group was produced from the copolymer solution of N-vinylformamide ( NVF) and acrylonitrile via wet spinning process.
将N-乙烯基甲酰胺(NVF)与丙烯腈(AN)的共聚物溶液进行湿法纺丝,制备了含氨基螯合纤维的前驱纤维。
2.
The NVF-DADMAC copolymer (PNVF-DA)was synthesized by aqueous solution polymerization with N-vinylformamide (NVF) and Diallyldimethylammonium chloride (DADMAC) using 2,2′-azobis(isobutyramidine)dihydrochloride(AIBA·2HCl)as the initiator.
以偶氮二异丁脒二盐酸盐(AIBA·2HCl)为引发剂,在水溶液中合成了N-乙烯基甲酰胺(NVF)与二甲基二烯丙基氯化铵(DADMAC)的共聚物,并对产物进行了FTIR、DSC表征。
3.
The cationic copolymers of NVF-DADMAC were synthesized by aqueous solution polymerization from N-vinylformamide(NVF) and Diallyldimethylammonium chloride(DADMAC).
以N-乙烯基甲酰胺(NVF)和二甲基二烯丙基氯化铵(DADMAC)为原料,通过水溶液聚合法合成了NVF-DADMAC阳离子共聚物。
4)  N-methyl acetamide
N-甲基乙酰胺
1.
Characterazation of α,ω-bis-(2-butanon oximoido) & α,ω -bis(N-methyl acetamide) PDMS by GC MS Analysis;
α,ω-二丁酮肟基聚二甲基硅氧烷和α,ω-二(N-甲基乙酰胺基)聚二甲基硅氧烷的表征
2.
N-vinyl-N-methyl-acetamide was synthesized from N-methyl acetamide and vinyl acetate with potassium hydroxide as catalyst.
以N-甲基乙酰胺、醋酸乙烯酯为原料,以氢氧化钾为催化剂合成了N-乙烯基-N-甲基乙酰胺。
5)  N-methyl-chloroacetamide
N-甲基氯乙酰胺
6)  N-methyl-acetanilide
N-甲基乙酰苯胺
补充资料:N-甲基乙酰胺
分子式:C3H7NO
分子量:73.10
CAS号:79-16-3

性质:白色针状结晶。熔点30.55℃(28℃),沸点206℃,140.5℃(12kPa),相对密度0.9571(25/4℃),折光率1.4301,闪点108℃。溶于水、乙醇、苯、醚、氯仿,不溶于石油醚。

制备方法:由乙酸乙酯与甲胺反应而得。将乙酸乙酯和65%的甲胺混合,加热至60℃左右,反应4昼夜,至不再有分层现象,即反应完毕。减压蒸馏回收乙醇,收集95-110℃(4.0kPa)馏分而得N-甲基乙酰胺。

用途:该品为农药、医药等有机合成的中间体。

说明:补充资料仅用于学习参考,请勿用于其它任何用途。
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