isobutyraldehyde

isobutyraldehyde的基本解释

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[化] 异丁醛

与isobutyraldehyde相关的网络例句 [注：此内容来源于网络，仅供参考]

The experimental results showed that SO_4 2-/TiO_2-MoO_3 was an excellent catalyst for synthesizing isobutyraldehyde glycol acetal .

研究了以固体超强酸SO42-/TiO2-MoO3为催化剂，异丁醛和乙二醇为原料，合成异丁醛乙二醇缩醛的反应条件。

Mainly engaged in: Hydrogen-imide hydrochloride, o-chlorophenyl cyclopentanone, 3.4 dimethoxy ethyl benzene, butyn single potassium acid, potassium ethyl malonyl, Ding amide, amide isobutyraldehyde , allyl chloroacetate, isopropyl chloroacetate Benzyl aluminum, cyclopentene, cyanide-o-chlorophenyl, o-methyl chloride, sulfuric acid chloride, p-chlorophenol, imidazole, Pinacolone, one chlorine Pinacolone.

主要经营：盐酸氢亚胺、邻氯苯基环戊酮、3.4二甲氧基苯乙酯、丁炔二酸单钾盐、丙二酸单乙酯钾盐、丁酰胺、异丁酰胺、氯乙酸烯丙酯、氯乙酸苄酯异丙醇铝、环戊烯、邻氯苯氰、邻氯苯甲酯氯、硫酸氯、对氯苯酚、咪唑、频呐酮、一氯频呐酮。

The reaction mechanism was suggested by way of isobutyraldehyde disproportionation first and followed by dehydrogenation of 2-methyl-1-propanol.

反应机理为经由在同一催化剂上先后进行醛歧化为酸和醇，醇再脱氢两步反应

The density of vacant sites on the surface of support has the effect on the dispersion state, surface acidity and catalytic activity of supported niobia catalysts for condensation reaction of isobutylene and isobutyraldehyde.

本工作较深入地描述了负载型铌氧化物催化剂表面相互作用，为深刻认识负载型铌氧化物催化剂酸催化作用和进行高效固体酸催化剂的设计和制备提供了参考依据。

FT-IR and 1H-NMR results show that the reaction occurs in the α-H atom of isobutyraldehyde.

FT-IR及1H-NMR结果说明合成反应发生在异丁醛中的α氢原子上。

与isobutyraldehyde相关的网络解释 [注：此内容来源于网络，仅供参考]

Isobutyraldehyde：异丁醛

接著,他们接合来自其他微生物的基因,以造出一种能吸收二氧化碳与阳光并产生异丁醛(isobutyraldehyde)气体的品种. 这种低沸点与高蒸汽压气体使其能轻易从系统中分离出来.

Isobutyraldehyde：异丁醛(增香剂)

isobtylene-isoprenecopolymer异丁橡胶;异丁烯一甲基丁二烯共聚物(咀嚼用胶基料) | isobutyraldehyde异丁醛(增香剂) | isobutyricacid异丁酸(增香剂)

Isobutyraldehyde：异丁基醛

Isobutylene 异丁烯 | Isobutyraldehyde 异丁基醛 | Isobutyric Acid 异丁酸

isobutyraldehyde oxime：异丁醛肟

异丁醛 isobutyraldehyde | 异丁醛肟 isobutyraldehyde oxime | 异丁醛缩胺脲 isobutyraldehyde semicarbazone

isobutyraldehyde semicarbazone：异丁醛缩胺脲

异丁醛肟 isobutyraldehyde oxime | 异丁醛缩胺脲 isobutyraldehyde semicarbazone | 异丁酰胺 isobutyramide; isobutyric amide