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1)  isocapro-lactone
异己内酯
2)  ε-Caprolactone
己内酯
1.
Two Dimensional Nuclear Magnetic Resonance Analysis on the Sequence Structure of Biodegradable Copolymer Derived from Trimethylene Carbonate and ε-Caprolactone;
三亚甲基碳酸酯和己内酯生物可降解共聚物序列结构的二维核磁分析
2.
Ring-open Polymerization of ε-Caprolactone Catalyzed by Substituted Indenyl Complexes;
取代茚基二价稀土配合物催化己内酯开环聚合反应
3.
Study on graft polymerization of ε-caprolactone onto cellulose acetate;
纤维素醋酸酯接枝己内酯的合成与表征
3)  poly(ε-caprolactone)
聚己内酯
1.
Study on poly(ε-caprolactone) scaffolds with multi-model pores through phase separation/salt leaching process;
聚己内酯多级孔径支架的相分离/盐析复合工艺研究
2.
Investigation on Isothermal and Non-isothermal Crystallization Kinetics of Poly(ε-caprolactone);
聚己内酯的等温与非等温结晶动力学研究
3.
Study on the Binary Blends of Poly(ε-caprolactone) with Different Cellulose Derivatives by Infrared Spectra;
聚己内酯与不同纤维素衍生物形成的共混体系的红外光谱研究
4)  polycaprolactone [,pɔli,kæprə'læktəun]
聚己内酯
1.
Synthesis of polycaprolactone-grafted-starch copolymer by tetrabutyl titanate;
钛酸四丁酯引发聚己内酯接枝改性淀粉的制备
2.
Study on preparation and biocompatibility of polycaprolactone nanofibers by electrospinning;
聚己内酯电纺纤维的制备及生物相容性研究
3.
Electrospinning: nanofiber from polycaprolactone (PCL);
聚己内酯(PCL)纳米纤维的静电纺丝
5)  ε-caprolactone
ε-己内酯
1.
Activation of calix [6] arene in the ring-opening polymerization of ε-caprolactone catalyzed by rare earth aryloxide catalysts in low temperature.;
杯[6]芳烃在芳氧基稀土(镧、钕)催化ε-己内酯低温开环聚合中的活化作用
2.
Ring-opening Polymerization of ε-Caprolactone Catalyzed by Rare Earth Trifluoromethanesulfonate [Ln(OTf)_3] Catalysts;
三氟甲磺酸稀土催化ε-己内酯开环聚合
3.
Vapor-phase dehydrogenation of 1,6-hexanediol to ε-caprolactone over CuO/Cr_2O_3/Al_2O_3 catalyst;
1,6-己二醇气相催化脱氢合成ε-己内酯的研究
6)  PCL
聚己内酯
1.
Study of Property of Shape Memory PCL/CaCO_3 Compound;
形状记忆材料聚己内酯复合材料性能研究
2.
Effect of Irradiation Modification on PCL;
辐照改性对聚己内酯的影响
3.
Synthesis, Characterization and Enzymatic Degradation of PCL-PLLA Block Copolymers;
聚乳酸—聚己内酯嵌段共聚物的合成、表征和酶降解
补充资料:异己内酯
分子式:
CAS号:

性质:又称异己内酯。无色液体,有芳香气味。凝固点10℃。沸点200~202℃(常压),95℃(2.666kPa)。相对密度d414.91.01661。折射率nD14.91.43490。能溶于2倍量的水中。与稀硝酸煮沸,可得γ-戊内酯-γ-羧酸,与氢氧化钾煮沸变成异己酸。与氨反应成4-羟基异己酰胺,后者与卤素酸反应可得4-卤代异己酸。以乙酰丙酸与2摩尔碘甲基镁作用制取,或蒸馏芸香酸制取。用作有机合成原料。

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