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二戊烯

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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。

In this paper, a series of 4,5-dithiacrown ether annulated 1,3-dithiole-2-thiones 8a~8d were prepared via condensing 4,5-bis-1,3-dithiole-2-thione (7) with 1,ω-dimercapto polyglycol derivatives in high dilution. The obvious template effect was found during the synthesis of 8c-8d.

在高度稀释条件下,经4,5-二溴甲基-1,3-二硫杂环戊烯-2-硫酮(7)和多缩乙二醇的1,ω-二巯基衍生物的缩合反应,方便地合成了4,5-位带二硫杂冠醚残基的2-硫代-1,3-二硫杂环戊烯的衍生物8a~8d,中间体硫杂冠醚8c~8d的合成中有明显的&模板效应&。

In this paper, a series of 4,5-dithiacrown ether annulated 1,3-dithiole-2-thiones 8a~8d were prepared via condensing 4,5-bis-1,3-dithiole-2-thione (7) with 1,ω-dimercapto polyglycol derivatives in high dilution. The obvious template effect was found during the synthesis of 8c-8d.

在高度稀释条件下,经4,5-二溴甲基-1,3-二硫杂环戊烯-2-硫酮(7)和多缩乙二醇的1,ω-二巰基衍生物的缩合反应,方便地合成了4,5-位带二硫杂冠醚残基的2-硫代-1,3-二硫杂环戊烯的衍生物8a~8d,中间体硫杂冠醚8c~8d的合成中有明显的&模板效应&。

ConclusionThe main components of liposoluble components are D-Limonene,-3,7-dimethyl-1,3,6-Octatriene,-2,6-dimethyl-2,4,6-Octatriene, Caryophyllene, 2,6-dimethyl-6-(4-methyl-3-pentenyl)-Bicyclo[3.1.1]hept-2-ene, alpha-Farnesene, and-2,6,10,15,19,23-hexamethyl-2,6,10,14,18,22-Tetracosahexaene.

结论蹄叶橐吾的脂溶性成分主要为D-柠檬烯(2.98%)、-3,7-二甲基-1,3,6-辛三烯(15.07%)、-2,6-二甲基-2,4,6-辛三烯(3.61%)、石竹烯(3.62%)、2,6-二甲基-6-(4-甲基-3-戊烯)-二环[3.1.1]庚-2-烯(6.20%)、α-法呢烯(4.09%)、反式角鲨烯(26.91%)等。

Water,caprylic/capric triglyceride,mineral oil,butylene glycol,stearic acid,acetylated lanolin,glycerin,ethylhexyl methoxycinnamate,dimethicone,polyisoprene,triethanolamine,cyclopentasiloxane,butyl methoxydibenzoylmethane,titanium dioxide,persea gratissima oil unsaponifiables,sodium DNA,borago officinalis seed oil,oenothera biennis oil,simmondsia chinensisseed oil,hydrolyzed RNA,tocopheryl acetate,urea,hydrolyzed extensin,retinyl palmitate,sodium hyaluronate,helianthus annuusseed oil,tocopherol,ascorbyl palmitate,ascorbic acid,lanolin alcohol,c12-20 acid peg-8 ester,cyclotetrasiloxane,glyceryl stearate,dimethiconol,ceteareth-20,carbomer,magnesium aluminum silicate,propylene glycol,peg-8,silica,BHT,citric acid,phenoxyethanol,methylparaben,butylparaben,ethylparaben,isobutylparaben,propylparaben,chlorhexidine digluconate

水,辛酸/癸酸三酸甘油酯,矿物油,丁二醇,硬脂酸,乙醯化羊毛脂,甘油,4-甲氧基肉桂酸-2-乙基己基酯,地美司康,聚异戊烯,三乙醇胺,环戊硅氧烷,丁基甲氧基二苯甲醯基甲烷,二氧化钛,酪梨油,DNA 钠盐,琉璃苣種子植物油,月见草油,荷荷巴籽油,水解RNA,醋酸盐维他命E,尿素,水解伸展蛋白,维他命A酯,透明质酸钠,葵花籽油,维生素E,抗坏血酸棕榈酸酯,维生素C衍生物,羊毛脂醇,C12-20 酸 PEG-8酯,环四硅氧烷,甘油硬脂酸,聚二甲基硅氧烷醇,鲸蜡硬脂醇醚-20,卡波姆,硅酸镁铝,丙二醇,聚乙二醇-8,二氧化硅,二丁基羟基甲苯,柠檬酸,苯氧乙醇,羟苯甲酯,羟苯丁酯,羟苯乙酯,羟苯甲酸异丁酯,羟苯丙酯,洗必泰葡萄糖酸盐

Given the current complexity of industrial recovery of 3'-methyl-2'-butenyl 3, 3-dimethyl-pentenoate and the decomposition problems with 2-methyl-1-butene, research was conducted on a process for direct recycling of MBDP involving an ester exchange reaction of MBDP with either methanol, trimethyl orthoacetate, or solutions of methanol and trimethyl orthoacetate.

针对目前工业上回收3,3-二甲基-4-戊烯酸-3'-甲基-2'-丁烯酯工艺复杂、异戊烯大量分解问题,研究了MBDP直接返回循环使用工艺,MBDP与甲醇、原乙酸三甲酯或与甲醇原乙酸三甲酯混合溶液进行酯交换反应的回收新工艺,比较了四异丙基钛酸酯、甲醇钠、氢氧化钾用作酯交换催化剂的效果,筛选出回收MBDP&一锅煮&最佳工艺:按照n:n:n:n=1.0:9.8:9.2:0.05物质的量比投料,74℃~78℃反应21h,MBDP转化为贲亭酸甲酯和异戊烯醇,单程转化率87.7%,用85%的磷酸中和甲醇钠,蒸出甲醇,直接用于合成贲亭酸甲酯。

By simulation, the optimal operation conditions were gained in every step in the separation process, and polymerization-class isoprene was gained by the process. And to improve the economy of process, the process was studied by simulation, 99% cyclopentene and 1, 3-pentadiene were gained by continuous separation process. All were the base of the process industrialization.

通过模拟研究,得到分离各步的最佳塔高,进料位置和各种操作条件;并进行了全流程的模拟优化得到聚合级的异戊二烯的各种工艺参数;通过模拟研究对分离工艺进一步深化,得到了从C5中分离出环戊烯和间戊二烯的优化工艺条件,对工艺经济性进一步优化,给过程工业化提供了依据。

Using W-HMS molecular sieve synthesized from the tungsten source of (NH4) 2WO4 as catalyst and hydrogen peroxide as oxidant, the effects of reaction time, temperature, dosage of catalyst, solvent type and volume, and oxidant concentration on the catalytic oxidation of cyclopentene to glutaraldehyde were investigated.

对以(NH4)2WO4为钨源合成的W-HMS分子筛为催化剂,过氧化氢为氧化剂,环戊烯合成戊二醛的多相催化反应进行了研究,考察反应时间、反应温度、催化剂用量、溶剂种类和用量以及氧化剂浓度等因素对戊二醛收率的影响。

Dicyclopentadiene ; Cyclopentadiene ; Raney Nickel ; Liquid hydrogenation ; Cyclopentene

双环戊二烯;环戊二烯;骨架镍;液相加氢;环戊烯

Bromo-2-sulfolene (2) reacted with substituted benzoic acid salt s 3a~3c or alizarin yellow (3d) to give four novel allylic substitution products 4a~4d by esterification reaction, respectively.

以3,4-二溴环戊砜(1)为原料,在无水吡啶作用下发生消除反应,得到反应中间体4-溴-2-环戊烯砜(2),再分别与一系列取代苯甲酸盐3a~3c以及茜素黄GG(3d)发生酯化反应,合成出4种新环戊烯砜衍生物4a~4d,并用IR,1HNMR,MS,元素分析等表征了它们的结构。

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