CAS: 111-34-2; N-Butyl Vinyl Ether

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CAS号74-86-2 乙炔 | CAS号71-36-3 正丁醇 | CAS号871-22-7 1-(1-丁氧基乙氧基)丁烷 | CAS号15898-92-7 6,6-dimethylhep... | CAS号81577-06-2 (2-butoxy-ethan... | CAS号17437-27-3 1-(1-butoxy-2-c... | CAS号75-01-4 乙烯基氯 | CAS号2372-45-4 正丁醇钠 | CAS号3999-70-0 potassium butanolate | CAS号1112-54-5 三乙基乙烯基硅烷 | CAS号109317-78-4 4-丁氧基-1,1,1-三氟-... | CAS号10496-13-6 BUTYL DICHLOROP... | CAS号1077-79-8 2-乙酰基苯甲酸甲酯 | CAS号60814-30-4 1-(喹啉-4-基)乙-1-酮 | CAS号34900-01-1 反式3-(N-甲基苯胺基)丙烯醛 | CAS号497-26-7 2-甲基-1,3-二氧戊环 | CAS号3665-80-3 N-乙基-对-硝基苯胺 | CAS号108-05-4 乙酸乙烯酯 | CAS号542-69-8 碘代正丁烷 | CAS号593-66-8 碘乙烯

乙二醇单丁醚置于sodium Hydroxide,乙醚,三溴化磷,2,3-二甲基苯胺体系中,化学反应生成乙烯基正丁醚
参考文献:Measuring New Zealand'S Gdp 1865-1933: A Cointegration-Based Approach
标题:Measuring New Zealand'S Gdp 1865-1933: A Cointegration-Based Approach
摘要:Official And Semi‐official Estimates Of New Zealand'S National Income Are Available On An Annual Basis For The Years Since 1932. Retrospective,Non‐official,Estimates Are Available From 1859. Chiefly These Are Constructed Following Doblin'S (1951) Pioneering Use Of Money Stock Data,Velocity,And The Implications Of The Quantity Theory Of Money,And Include The Estimates Of Hawke (1975),Rankin (1992) And Cashin (1995).This Paper Estimates New Zealand Real Gdp Per Capita With Monetary Data Using Valid,Intervention‐free,Cointegration Methods. The New Measures Avoid The Ad Hoc Adjustments Found In Rankin (1992),Yet Unlike Cashin (1995),They Incoporate Specific New Zealand Monetary Features. The New Time Series Conform Well With Independent Benchmarks And The Historiography Of The Pre‐1914 Period. Alternatively,They Suggest An Interpretation Of New Zealand'S Growth Experience For Years Around World War One Which Differs From That Of Australia,And From The Findings Of Rankin (1992) And Cashin (1995).
Doi:10.1111/j.1475-4991.2000.Tb00847.X

专利信息

专利号:US-5118853-A
优先权日:1988-10-13
标题:Processes for the synthesis of 3-disubstituted aminoacroleins
发明人：LEE GEORGE T; REPIC OLJAN
权利人:SANDOZ LTD
摘要:Process for the synthesis of compounds of the formula ##STR1## comprising the steps of (i) reacting a compound of the formula ##STR2## with oxalyl chloride or oxalyl bromide to form the corresponding compound of the formula ##STR3## (ii) reacting said compound of the formula ##STR4## with a compound of the formula ##STR5## to form the corresponding compound of the formula ##STR6## (iii) hydrolyzing said compound of the formula ##STR7## to obtain the corresponding compound of the formula ##STR8## the use of the compounds of the formula ##STR9## for the synthesis of the compounds of the formula ##STR10## and the use of the intermediates of Formula VII for the direct synthesis of the compounds of Formula II, n wherein n R 1 is C 1-3 alkyl, phenyl or phenyl substituted by 1 to 3 substituents each of which is independently C 1-3 alkyl, C 1-3 alkoxy, fluoro, chloro, bromo or nitro (maximum of two nitro groups), n R 1b is phenyl or phenyl substituted by 1 to 3 substituents each of which is independently C 1-3 alkyl, C 1-3 alkoxy, fluoro, chloro, bromo or nitro (maximum of two nitro groups), n R 2 is C 1-3 alkyl, n one of R 3 and R 4 is ##STR11## and the other is primary or secondary C 1-6 alkyl not containing an asymmetric carbon atom, C 3-6 cycloalkyl or phenyl-(CH 2 ) m -, n wherein n R 7 is hydrogen, C 1-3 alkyl, n-butyl, i-butyl, t-butyl, C 1-3 alkoxy, n-butoxy, i-butoxy, trifluoromethyl, fluoro, chloro, phenoxy or benzyloxy, n R 8 is hydrogen, C 1-3 alkyl, C 1-3 alkoxy, trifluoromethyl, fluoro, chloro, phenoxy or benzyloxy, n R 9 is hydrogen, C 1-2 alkyl, C 1-2 alkoxy, fluoro or chloro, and n m is 1, 2 or 3, with the provisos that not more than one of R 7 and R 8 is trifluoromethyl, not more than one of R 7 and R 8 is phenoxy, and not more than one of R 7 and R 8 is benzyloxy, n R 5 is hydrogen, C 1-3 alkyl, n-butyl, i-butyl, t-butyl, C 3-6 cycloalkyl, C 1-3 alkoxy, n-butoxy, i-butoxy, trifluoromethyl, fluoro, chloro, phenoxy or benzyloxy, and n R 6 is hydrogen, C 1-3 alkyl, C 1-3 alkoxy, trifluoromethyl, fluoro, chloro, phenoxy, or benzyloxy, with the provisos that not more than one of R 5 and R 6 is trifluoromethyl, not more than one of R 5 and R 6 is phenoxy, and not more than one of R 5 and R 6 is benzyloxy, n R 10 is C 1-6 alkyl, each X is chloro or bromo, and each X.sup.⊖ is chloride or bromide.

专利号:US-11465970-B2
优先权日:2017-12-14
标题 :Method for synthesis of Roxadustat and intermediate compounds thereof
发明人：XU YONGXIANG
权利人:NANJING CAVENDISH BIO ENGINEERING TECH CO LTD; XU YONGXIANG; NANJING CAVENDISH BIO ENG TECH CO LTD
摘要:The present application provides a method for synthesis of Roxadustat. A compound as represented by formula (VIII) is used as a raw material, and is reacted with phenol, a vinyl-containing ether, an acid, hydroxylamine, and then the product is reacted with glycine. In addition, the present application also provides intermediate compounds as represented by formula (IX), formula (XI), formula (XII), formula (IV), and formula (V) for synthesis of Roxadustat. Herein, details of the substituents involved in formula (VIII), formula (IX), formula (XI), and formula (XII) are stated in the description

专利号:EP-0842924-B1
优先权日:1996-11-14
标 题 :Pyridine intermediates, useful in the synthesis of beta-adrenergic receptor agonists
发明人：WRIGHT STEPHEN WAYNE
权利人:PFIZER
摘要:The present invention relates to certain compounds of the formula (I), which are useful in the synthesis of certain beta -adrenergic receptor agonists. The invention also relates to a process for synthesizing the compounds of formula (I) and to compounds of the formula (II), wherein R<1>, R<2> and R<4> are defined herein, which are useful in the synthesis of the compounds of formula (I). The invention also relates to a process for synthesizing a compound of formula (II). The invention further relates to processes for synthesizing compounds of formula (Z*), R<1>, R<2> and Y<2*> are defined herein.o

专利号:US-5290946-A
优先权日:1988-10-13
标 题 :Processes for the synthesis of 3-(substituted indolyl-2-yl)propenaldehydes
发明人：LEE GEORGE T; KAPA PRASAD K; REPIC OLJAN
权利人:SANDOZ LTD
摘要:A process for synthesizing compounds of the formula ##STR1## utilizing, as intermediates, oxalyl chloride or bromide and compounds of the formulae R 1 R 2 N--CHO and CH 2 â•?CH--O--R 10 are processes for synthesizing compounds of the formula ##STR2## utilizing, as intermediates, compounds of Formula I wherein R 1 is phenyl or substituted phenyl or intermediates in the synthesis of the compounds of formula I which intermediates have the formula ##STR3## wherein R 1 is C 1-3 alkyl, phenyl or phenyl substituted by 1 to 3 substituents each of which is independently C 1-3 alkyl, C 1-3 alkoxy, fluoro, chloro, bromo or nitro (maximum of two nitro groups), n R 2 is C 1-3 alkyl, n R 10 is C 1-6 alkyl, n X.sup.⊖ is chloride or bromide, and n R 3 -R 6 are as defined in the specification. n The compounds of Formula II are intermediates in the synthesis of known HMB-CoA reductase inhibitors which inhibit the biosynthesis of cholesterol and are useful as antihyperchloesterolemic gents.

专利号:US-4794199-A
优先权日:1984-07-05
标题:Process for synthesis of primary amines from olefins, syngas and ammonia
发明人：LIN JIANG-JEN; KNIFTON JOHN F
权利人:TEXACO INC
摘要:This invention concerns the synthesis of primary amines from olefins, synthesis gas and ammonia via an amination process in the presence of a cobalt catalyst, an ether solvent and a tertiary group VB donor ligand.

专利号:US-10870649-B2
优先权日:2017-04-13
标题:Synthesis of NIR fluorescent probe
发明人：LATTUADA LUCIANO; BUONSANTI FEDERICA; CRIVELLIN FEDERICO; FERRETTI FULVIO; MAISANO FEDERICO; ORIO LAURA; PIZZUTO LORENA
权利人:BRACCO IMAGING SPA
摘要:The application relates to a process for the synthesis of a Near Infra-Red (NIR) fluorescent probe which is a cRGD-Cy5.5 conjugate of formula (I) known as DA364 comprising an aza-bicycloalkane based cyclic peptide labelled with a Cy5.5 dye moiety and used in the guided surgery of tumors and pathologic regions.