- 更多网络例句与二戊烯相关的网络例句 [注:此内容来源于网络,仅供参考]
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The production methods of glutaraldehyde,including those of addition reaction of acraldehyde , oxidation of 1,5-pentadiol,reduction of glutaryl chloride and oxidation of cyclopentene,are summarized.
综述了丙烯醛加成、 1,5 -戊二醇氧化、戊二酰氯还原和环戊烯氧化等戊二醛的合成路线和制备方法,考察了目前戊二醛的生产厂家及其在皮革鞣剂、油田注水杀菌剂和医药杀菌等领域的应用市
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The cytotoxicity of these compounds were valuated by MTT and SRB methods using three cancer cell lines: HL-60, A-549, P-388. Cyclo-shikonin, and cyclo-alkannin have high cytotoxicity against HL-60.The chiral center of side chain has no effect on their activity. 2- 1-(Acetyloxy-4-methyl-3-pentenyl -5, 8-dihydroxy-1, 4-naphthoquinone (105) has strong inhibition effect on P-388 cells. 2- 1-(isooctyloxy-4-methyl-3-pentenyl -5, 8-dihydroxy-1, 4-naphthoquinone (108) and 2- 1-(2-furoyloxy-4-methyl-3-pentenyl -5, 8-dihydroxy-1, 4-naphthoquinone (112) have high inhibition on A-549.Shikonin (1), alkannin (2), and their derivatives have the structural features of a planar chromophores and short side chain. We examined the ability to inhibit the telomerase.
抗肿瘤活性初步筛选测试采用小鼠白血病P-388肿瘤细胞和人肺癌A-549肿瘤细胞进行,结果表明侧链羟基的手性对抗肿瘤活性无明显影响;有数个化合物具有很好的体外抑制活性,特别是化合物2-(1-异辛酰氧基-4-甲基-3-戊烯基)-5,8-二羟基-1,4-萘醌(108)和2-[1-(2-呋喃甲酰氧基)-4-甲基-3-戊烯基]-5,8-二羟基-1,4-萘醌(112)体外显示对人肺癌A-549肿瘤细胞有强效;2-(1-乙酰氧基-4-甲基-3-戊烯基)-5,8-二羟基-1,4-萘醌(105)对小鼠白血病P-388肿瘤细胞有强效;环紫草素和环异紫草素对人白血病HL-60细胞有强烈抑制作用。
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They were eucalyptol, bicyclo[2.2.1]heptan-2-one,1,7,7-trimethyl-,(1R)-, borneol, 1-methyl-2-(1-methyl ethenyl)-(1R-cis)-cyclobutaneethanol, limonene, 1-hydroxymethyl-7,7-dimethy lbicyclo[2.2.1]heptan-2-one,-spathulenol, 3,7,11,15-Tetramethyl-2-hexadecen-1-ol, isocitronellol,-9-Octadecenoic acid, heneicosane, respectively.
阿给中共有11个阿给炭没有检测出的成分,包括桉油精、D-樟脑、冰片、(1R-cis)- 1-甲基-2-(1-甲基乙烯基)环丁基乙醇、二戊烯、1-羟甲基-7,7-二甲基-双环[2.2.1]庚-2-酮、-匙叶桉油烯醇、3,7,11,15-四甲基-2-十六碳烯-1-醇、异香茅醇、-9-十八碳烯酸和廿一烷。
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The results showed: at the reaction temperature of 25~30 ℃,hydrogen pressure of 1.0~1.5 MPa,Vethanol∶Vcyclopentadiene of 5~6∶1,the catalyst dosage of 4 %~5 % and stirring rate of 800 r/min.The conversion of cyclopentadiene was above 98% and the selec...
结果表明,在反应温度25-30℃,氢气分压为1.0-1.5 MPa,无水乙醇作为溶剂,V无水乙醇∶V环戊二烯为5-6∶1,催化剂用量为4%-5%,搅拌速度为800 r/min条件下,反应时间2~3 h,环戊二烯的转化率大于98%,环戊烯的选择性大于95%。
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The studies on production of pure cyclopentadiene by depolymerization-rectify of technical dicyclopentadiene and the influenceable factors about preparation of cyclopentene by liquid hydrogenation of cyclopentadiene at the Raney Nickel catalyst were carried out.
介绍了以工业级双环戊二烯为原料,经过解聚-精馏得到高纯度的环戊二烯,以骨架镍为催化剂,对环戊二烯液相加氢制备环戊烯的影响因素进行了研究。
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Studies on the novel catalytic materials used in catalytic oxidation of cyclopentene to glutaraldehydeKeywords: Cyclopentene,Catalytic oxidation,Glutaraldehyde,Mesoporous zeolite,Titania,Spheroi
环戊烯合成戊二醛催化新材料的研究关键词:环戊烯,催化氧化,戊二醛,介孔分子筛,二氧化钛,微
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The double bond in norbornene ring of TCPD was easily saturated at a low temperature, and an intermediate 12,13-dihydrotricyclopentadiene (12,13-DHTCPD) was formed. Higher temperature and hydrogen pressure were required for the saturation of remaining double bond in cyclopentene ring to generate a completely hydrogenated compound tetrahydrotricyclopentadiene.That is to say, the reaction occurred via the TCPD→12,13-DHTCPD→THTCPD route.
采用气质联用、红外光谱和核磁共振对加氢产物进行表征,发现在加氢反应中TCPD的降冰片烯双键首先被饱和,生成中间产物12,13-二氢三环戊二烯(12,13-DHTCPD),残留的环戊烯双键需要在更高的温度和氢压下反应生成四氢三环戊二烯,即反应按照TCPD→12,13-DHTCPD→THTCPD的途径进行。
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The major products were methane, ethylene, propylene, butylene, butadiene, cyclopentadiene, benzene, toluene, styrene, vinyl-substituted cyclopentene derivatives and C5/C6 isomers (pentadiene, methyl-substituted cyclopentene derivatives, cyclohexene, hexadiene and methyl-substituted cyclopentadiene derivatives), and the main primary products were determined to be C1~C4 compounds, cyclopentadiene, benzene, toluene and vinyl-substituted cyclopentene derivatives.
热裂解主要产物为甲烷、乙烯、丙烯、丁烯、丁二烯、环戊二烯、苯、甲苯、苯乙烯、环戊烯的乙烯基取代物及C5, C6异构体(戊二烯、环戊烯的甲基取代物、环己烯、己二烯和环戊二烯甲基取代物),其中, C1~C4、环戊二烯、苯、甲苯、乙烯基取代环戊烯为初始产物。
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The major products were methane, ethylene, propylene, butylene, butadiene, cyclopentadiene, benzene, toluene, styrene, vinyl-substituted cyclopentene derivatives and C5/C6 isomers pentadiene, met...
热裂解主要产物为甲烷、乙烯、丙烯、丁烯、丁二烯、环戊二烯、苯、甲苯、苯乙烯、环戊烯的乙烯基取代物及C5,C6异构体(戊二烯、环戊烯的甲基取代物、环己烯、己二烯和环戊二烯甲基取代物),其中,C1~C4、环戊二烯、苯、甲苯、乙烯基取代环戊烯为初始产物。
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These compounds were identified as follows:chrysophanol (FP-1),physcion(FP-2),eriosematin(FP-3),scoparone(FP-4),lupeol(FP-5),betulinic acid(FP-6),3\',4\'-Dihydroxy-trans-cinamic acid octacosyl ester(FP-7),β-sitosterol (FP-8),flemiphilippinone A(FP-9),monopalmitin(FP-10),emodin(FP-11),islandicin (FP-12),salicylic acid(FP-13),p-methoxyphenylpropionic acid(FP-14),trideca-1, 3-diene(FP-15),lupinifolin(FP-16),flemichin D(FP-17),flemiphilippinin A(FP-18), auriculasin(FP-19),erythrinin B(FP-20),6-C-prenylluteolin(FP-21), 8-(1,1-dimethylallyl) genistein(FP-22),flemiphilippinin E(FP-23),flemiphilippinin F (FP-24),5,7,3\',4\'-tetrahydroxy-6,8-diprenylisoflavone(FP-25),flemiphilippinin D (FP-26),dorsmaninsⅠ(FP-27),osajin(FP-28),6,8-diprenyleriodictyol(FP-29), lupinalbin A(FP-30),genistein(FP-31),3\'-O-methylorobol(FP-32),orobol(FP-33), 5,7,2\',3\',4\'-pentahrdroxyflavone(FP-34),the mixture of biochanin A and prunetin (FP-35 and 36),genistin(FP-37),sophororicoside(FP-38),3\'-O-methylorobol-7-glucoside(FP-39),the mixture of sissotrin and prunetin 4\'-O-β-D-glucoside(FP-40 and 41),adenosine(FP-42) and luteoloside(FP-43,mixture).
这些化合物分别为大黄酚(FP-1)、大黄素甲醚(FP-2)、eriosematin(FP-3)、滨蒿内酯(FP-4)、羽扇豆醇(FP-5)、白桦酸(FP-6)、咖啡酸二十八烷酯(FP-7)、β-谷甾醇(FP-8)、蔓性千斤拔酮A(FP-9)、单棕榈酸甘油酯(FP-10)、大黄素(FP-11)、islandicin(FP-12)、水杨酸(FP-13)、对甲氧基苯丙酸(FP-14)、十三烷-1,4-二烯烃(FP-15)、lupinifolin(FP-16)、千斤拔素D(FP-17)、蔓性千斤拔素A(FP-18)、auriculasin(FP-19)、erythrinin B(FP-20)、6-C-异戊烯基木犀草素(FP-21)、8-(1,1-二甲烯丙基)-染料木黄酮(FP-22)、蔓性千斤拔素E(FP-23)、蔓性千斤拔素F(FP-24)、5,7,3′,4′-四羟基-6,8-双异戊烯基异黄酮(FP-25)、蔓性千斤拔素D(FP-26)、dorsmaninsⅠ(FP-27)、osajin(FP-28)、6,8-双异戊烯基圣草素(FP-29)、lupinalbin A(FP-30)、染料木黄酮(FP-31)、3\'-O-甲基香豌豆苷元(FP-32)、奥洛醇(FP-33)、5,7,2′,3′,4′-五羟基黄酮(FP-34)、鹰嘴豆素甲和樱黄素的混合物(FP-35和FP-36)、染料木苷(FP-37)、槐属苷(FP-38)、7-葡萄糖基-3\'-O-甲基香豌豆苷(FP-39)、印度黄檀苷和樱黄素4′-O-β-D-葡萄糖苷的混合物(FP-40和FP-41)、腺嘌呤核苷(FP-42)和木犀草苷(FP-43,混合物)。
- 更多网络解释与二戊烯相关的网络解释 [注:此内容来源于网络,仅供参考]
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Codeine cyclopentenylallylbarbiturate:环戊烯基丙烯基巴比土酸可待因
Codeine cyclohexenylethylbarbiturate;环乙烯基乙基巴比土酸可待因;; | Codeine cyclopentenylallylbarbiturate;环戊烯基丙烯基巴比土酸可待因;; | Codeine diallylbarbiturate;二丙烯基巴比土酸可待因;;
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cyclopentane:環戊烯
cyclopentadienyl環戊二烯基 | cyclopentane環戊烷 | cyclopentane環戊烯
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TETRAMETHYL CYCLOPENTENE BUTENOL:四甲基環戊烯丁烯醇
TETRAMETHYLCHROMANOL GLUCOSIDES四甲基苯並二氫吡喃醇葡糖苷類 | TETRAMETHYL CYCLOPENTENE BUTENOL四甲基環戊烯丁烯醇 | TETRAMETHYL DECYNEDIOL四甲基癸炔二醇
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dipentene:二戊烯
0~80%、肉豆蔻醚(Myristicin)约4%、丁香酚(Eugenol)、异丁香酚、甲基丁香酚、甲氧基丁香酚、甲氧基异丁香酚、黄樟醚(Safrol)、榄香脂素(Elemicin)、异三甲氧基苯丙烯、α-侧柏烯(α-Thujene)、Δ3-蒈烯(Carene)、二戊烯(Dipentene)、香叶醇(Gera
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dipentene:二聚戊烯
dipcompassgradiograph 测斜仪 | dipentene 二聚戊烯 | dipentene 二戊烯
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dipentene monoxide:单氧双戊烯
"dipentene","双戊烯" | "dipentene monoxide","单氧双戊烯" | "diphenol","二酚"
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dipentene; limonene; p-mentha-1,8-diene:双戊烯;薴;柠檬油精;对[草(之上)+孟]-1,8-二烯
四硫化双(五亚甲胺硫酰基) dipentamethylenethiuram tetrasulfide | 双戊烯;薴;柠檬油精;对[草(之上)+孟]-1,8-二烯 dipentene; limonene; p-mentha-1,8-diene | 双(苯乙酮);双(苄酰甲基) diphenacyl
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pentadiene:戊二烯 戊烯
pentadelphousstamen五体雄蕊 | pentadiene戊二烯 戊烯 | pentadienoicacid戊二烯酸
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dimethyl pentene:二甲基戊烯
dimethyl pentane 二甲基戊烷 | dimethyl pentene 二甲基戊烯 | dimethyl phenol 二甲酚
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diamyl:二戊基;联戊基
diamyl tartrate 酒石酸二戊酯 | diamyl 二戊基;联戊基 | diamylene 癸烯;二戊烯基;萜烯