CAS: 15721-22-9; 2,2-Dimethylvaleroylchloride

上下游产品

CAS号1185-39-3 2,2-二甲基戊酸 | CAS号14458-05-0 2,3,5,6-4四甲基对苯二甲酸 | CAS号406235-30-1 N-B°C-4-甲基-4-羟基哌啶 | CAS号352-13-6 4-氟苯基溴化镁 | CAS号13146-45-7 (2,2-Dimethylva... | CAS号13146-36-6 2,2-dimethylval...

📜Alkaline Earth Salt Of/the/ Methylsulfuric Acid置于氯化亚砜体系中,化学反应生成新庚酰氯
参考文献:Locquin; Leers,Comptes Rendus Hebdomadaires Des Seances De L'Academie Des Sciences,1924,Vol. 178,P. 2097
标题:Locquin; Leers,Comptes Rendus Hebdomadaires Des Seances De L'Academie Des Sciences,1924,Vol. 178,P. 2097

专利信息

专利号:US-2019031702-A1
优先权日:2016-03-14
标 题 :Compounds and Methods for the Synthesis of 5-(N-Protected-Tryptaminocarboxyamide)-2'-Deoxyuridine Phosphoramidate for Incorporation into a Nucleic Sequence

专利号:WO-2017160672-A1
优先权日:2016-03-14
标题:Compounds and methods for the synthesis of 5-(n-protected-tryptaminocarboxyamide)-2'-deoxyuridine phosphoramidate for incorporation into a nucleic sequence

专利号:US-5827855-A
优先权日:1992-12-28
标题 :Hexahydronaphthalene ester derivatives their preparation and their therapeutic uses
发明人：KOGEN HIROSHI; ISHIHARA SADAO; KOGA TEIICHIRO; KITAZAWA EIICHI; SERIZAWA NOBUFUSA; HAMANO KIYOSHI
权利人:SANKYO CO
摘要:Compounds of formula (I): (I) wherein R1 represents a group of formula (II) or (III): (II) (III) R2 is alkyl, alkenyl or alkynyl; R3 and R4 are each hydrogen, alkyl, alkenyl or alkynyl; R5 is hydrogen or a carboxy-protecting group; Ra is a group of formula -OR6; R6 is hydrogen; R6a and R6b are each hydrogen, a hydroxy-protecting group, alkyl, alkanesulfonyl, halogenated alkanesulfonyl or arysulfonyl, and their salts and esters. Such compounds inhibit the synthesis of cholesterol, and can be used for the treatment and prophylaxis of hypercholesterolemia and of various cardiac disorders.

专利号:US-7576245-B2
优先权日:2002-07-11
标题:Fluorous tagging and scavenging reactants and methods of synthesis and use thereof
发明人：ZHANG WEI; LUO ZHIYONG
权利人:FLUOROUS TECHNOLOGIES INC
摘要:The present invention includes methods and compositions for increasing the fluorous nature of an organic compound by reacting it with at least one fluorous compound to produce a fluorous tagged organic compound. The increased fluorous nature of the fluorous tagged organic compound can then be utilized to separate the fluorous organic compound from untagged reagents, reactants, catalysts and/or products derived therefrom. The resultant fluorous tagged organic compound can be subjected to subsequent chemical transformations, wherein the fluorous nature of the tagged compound is utilized to increase the ease of separation of the fluorous tagged organic compound from untagged reagents, reactants, catalysts and/or products derived therefrom, after each chemical transformation. The chemical transformations result in a second fluorous tagged organic compound wherein the fluorous nature of the second fluorous tagged organic compound can then be reduced by removing the fluorous group therefrom, thereby producing a second organic compound that may be employed as a pharmaceutical compound or intermediate, or a combinatorial library component.

专利号:EP-3430022-A1
优先权日:2016-03-14
标题 :Compounds and methods for the synthesis of 5-(n-protected-tryptaminocarboxyamide)-2'-deoxyuridine phosphoramidate for incorporation into a nucleic sequence

专利号:CN-108779140-B
优先权日:2016-03-14
标 题 :Compounds and methods for the synthesis of 5-(N-protected tryptoaminocarboxamide)-2'-deoxyuridine phosphoramidite for incorporation into nucleic acid sequences