氟化酰 的英文怎麼說
中文拼音 [fúhuà]-
Silica pigment, benzene parazolone, oxalic acid catalyzer, accelerant, catalyst, deposit carbon powder, starch, paraacetaminophenetol - sulfonamide, sodiumpara - aminosalicylate ( pasna ), dalmato, p - thephalic acid, diethylbenzene - amine, titanium dioxide, acticarbon, sodium fluosilicate, fluorite, by - thiamine, silica gel powder, synthetic resin, sulfonic acid, polypropylene resin, aureomycin, pyrosodium silicate, gluchlorine acid coffee grounds, glucose, sodium sulfate, sulfide mineral, guound phosphate rock, bb, p. v. c.,
M 、觸媒、沉澱炭粉、對乙酰氮基苯磺酰氨、對氨基水楊酸、哆耳瑪托、對苯二酸、二乙苯銨、二氧化鈦、活性碳、氟硅酸鈉、氟石礦、副產硫銨、硅膠粉未、合成樹脂、磷酸鈣、聚丙烯樹脂、金黴素、偏硅酸鈉、糠氯酸咖啡渣、口服葡萄糠、硫酸鈉、硫化礦、磷礦粉、蘭bb 、 p . vThis product had strong property of separation and recovery of organic dissolvent and vapour, such as ether, ketone, alcohol, thf, dichlorotetra, chlorolform, narkosid, carbon disulfide disulphide, carbon, benzol, gasoline oil, etc
對醚類、酮類、醇類、四氫呋喃、二氯四烷、三氯甲烷、三氯乙烯、二硫化碳、苯、甲苯、甲酰、汽油及含汞、含氟烴類有機溶劑和有機蒸氣有很強的分離、回收性能。This paper describes fluopicolide, a new fungicide for control of oomycete diseases such as downy mildew and late blight, providing its chemical name, physical and chemical properties, toxicity, route of discovery, mechanism of action, efficacy, patent status, and synthesis methodology
摘要介紹了防治卵菌綱病害如霜霉病和晚疫病的殺菌劑氟啶酰菌胺,內容涉及化學名稱、理化性質、毒性、創制經緯、作用機理、藥效結果、專利概況與合成方法等。Perfluoroguanidine can be prepared by the direct fluorination of dry ammeline with 5% fluorine at about-16℃.
全氟胍可以由乾的三聚氰酰胺,用5的氟,在約16直接進行氟化而制得。Perfluoroguanidine can be prepared by the direct fluorination of dry ammeline with 5% fluorine at about -16℃.
全氟胍可以由於的三聚氰酰胺,用5的氟在約16直接進行氟化制得。In particular, the resulting active ester with pentafluorophenol facilitated the subsequent reaction with an amine and the hydrazine derivative to yield the c - terminal amide and hydrazide, respectively
特別是與五氟苯酚生成的酯對后續的與氨或肼衍生化分別生成c端酰胺或酰肼非常有利。Study on the macrokinetics of catalytic reaction of sulfuryl fluoride synthesis
催化合成硫酰氟宏觀反應動力學研究Methods linezolid was prepared by the steps of substitution, reduction, acylation and condensation with biacetyl compond from the starting material 3, 4 - difluoronotrobenzene
方法以3 , 4 -二氟硝基苯為原料,經取代、還原、酰化、再與側鏈雙乙酰化合物縮合得到目標化合物。Synthesis and biological activity of n - aryl - n - o - nitrobenzoyl thiourea derivatives
二氟苯甲酰基硫脲化合物的合成與除草活性研究This paper discusses methods of synthesizing fomesafen technical having high active ingredient percentages, with special emphasis on the key processes of nitration and acylation, and with the goal of manufacturing low cost fomesafen technical with > 98 % purity
摘要討論了高含量氟磺胺草醚原藥的合成方法,對關鍵的硝化與酰化工藝進行了探討,使其在較低生產成本下合成98 %以上的氟磺胺草醚原藥。Determination of the uranium content in nuclear grade uranium hexafluoride, uranyl fluoride solutions, uranyl nitrate solutions, uranium oxide, uranium dioxide, powder and pellets ; gravimetric method
核純級的六氟化鈾氟化鈾酰溶液硝酸雙氧鈾溶液< uk > perfluoroguanidine can be prepared by the direct fluorination of dry ammeline with 5 % fluorine at about - 16. < / uk >
< uk >全氟胍可以由於的三聚氰酰胺,用5的氟在約16直接進行氟化制得。 < / uk >Fluoroalkyl acetic acids were converted to their corresponding carbonyl chlorides, which was then reacted with o - amino benzaldehyde and ammonia gas to give 3 - ( 1 - iminofluoroalkyl ) - 1h - qunolin - 2 - ones in moderate yields
摘要用2 -氟烷基乙酸為初始原料,用氯化亞碸或五氯化磷將其轉化為相應的酰氯,後者在室溫與鄰胺基苯甲醛縮合,通入氨氣迴流反應得到3 - ( 1 -亞胺基氟烷基) 1h -喹啉2 -酮類化合物,產率中等。Producer of cobalt, nickel, and copper salts in china. products include oxides, chlorides, sulfates, nitrates, acetates, and aminosulfonates
-生產氯乙酰氯氯乙酸氫氟酸鹽酸等無機化工品,提供相關的產品技術標準檢驗方法和儲存及運輸要求。分享友人