CAS: 112-16-3; Lauroyl Chloride

上下游产品

phosgene lauric acid oxalyl dichloride dodecanehydrazide1-bromo-tridecan-2-one NSC 3172 1,4-dilauroyl-piperazine Retinyl laurate

月桂酸置于氯化亚砜体系中,化学反应 0.25H,反应生成月桂酰氯
参考文献:饱和羟基脂肪酸的简明合成和ffa1,Ffa4和gpr84上所有羟基金酸的体外评价
标题:饱和羟基脂肪酸的简明合成和ffa1,Ffa4和gpr84上所有羟基金酸的体外评价
摘要:饱和的羟基脂肪酸构成了一类尚未开发的脂质,具有潜在的有趣的生物学活性.我们报告了一种简明且通用的合成路线,以饱和的羟基脂肪酸在位置6或更高位置被羟基化,并以羟基金酸的合成为例.在游离脂肪酸受体ffa1,Ffa4和gpr84上测试了所有羟基金酸的区域异构体.结果表明,羟基的引入及其位置对受体活性有很大的影响.
Doi:10.1039/c7Md00130D

专利信息

专利号:US-5780658-A
优先权日:1995-01-10
标 题 :Process for the synthesis of cationic surfactants comprising esterification with basic character amino acids
发明人：MARTINEZ-PARDO MARTA ROSA INFA; MESTRES AUGUSTIN CONTIJOCH; SERRABASA PILAR ERRA
权利人:MIRET LAB
摘要:The process of the invention is directed to the synthesis of cationic type surfactant compounds consisting of natural basic-character amino acids, and any of their homologs, suitably modified for the purpose of obtaining products having specific applications as antimicrobial (biocidal) agents. The process comprises a first step of esterification of an amino acid, and a second step of the condensation of a fatty acid chloride with an esterified amino acid derivative. Nontoxic reaction media and catalysts are used, and a final product free from impurities is obtained. The cost of the process of the invention is reduced from prior art processes due to the use of cheaper starting materials and simpler equipment.

专利号:US-10287242-B2
优先权日:2011-12-28
标 题:Process for the synthesis of highly pure cationic surfactant products
发明人：MEHTA DILIP S; SHASTRI MAYANK
权利人:MEHTA DILIP S; SHASTRI MAYANK; ORGANISTRY LLC
摘要:The present invention is related to synthesis of highly pure cationic surfactant products by eliminating or reducing impurities generation that has beset prior art. This is achieved through the N-acylation of ester of amino acid and its inorganic salts or its organic salts (e.g. amino acid or hydrochloride of amino acid or sulfate of amino acid or acetate of amino acid etc.) in non-hydrolytic or nearly non-hydrolytic reaction conditions involving mono or biphasic reaction system with fatty acid halide (C 4 to C 20 ), under moderate uniform basic condition yielding high purity N-acyl substituted amino acid ester, particularly ethyl lauroyl arginate. The present process achieves pH control through process strategy rather than the measurement and control steps. This ambient temperature process is stable through a range of temperature variation eliminating rigid low temperature control.

专利号:US-7189849-B2
优先权日:1997-02-10
标 题:Synthesis of acyclic nucleoside derivatives
发明人：LEANNA M ROBERT; RASMUSSEN MICHAEL; HANNICK STEVEN M; TIEN JIEN-HEH J; LUKIN KIRILL A; TIAN ZHENPING; CHANG SOU-JEN; CURTY CYNTHIA B; NARAYANAN BIKSHANDARKOIL A; BELLETTINI JOHN; SHELAT BHADRA; SPITZ TIFFANY
权利人:MEDIVIR AB
摘要:Novel processes towards the synthesis of the antiviral valomaciclovir stearate in which an esterified guanine acetal is reduced to the corresponding alcohol, reacted with an activated amino acid and N-deprotected. The esterified guanine acetal is prepared from a 9-guanine derivative bearing an acyclic hydroxymethylbutylacetal. The processes are amendable to one-pot reactions.

专利号:US-3959322-A
优先权日:1960-09-22
标 题:Synthesis of 13-alkyl-gon-4-ones
发明人：HUGHES GORDON ALAN; SMITH HERCHEL
权利人:SMITH HERCHEL
摘要:The preparation of 13-methylgon-4-enes and novel 13-polycarbonalkylgon-4-enes by a new total synthesis is described. 13-Alkylgon-4-enes having progestational, anabolic and androgenic activities are prepared by forming a tetracylic gonane structure unsaturated in the 1,3,5(10),9(11) and 14-positions, selectively reducing in the B- and C-rings, and converting the aromatic A-ring compounds so-produced to gon-4-enes by Birch reduction and hydrolysis.

专利号:US-6229055-B1
优先权日:1996-04-12
标题 :Synthesis of fluorinated xanthene derivatives
发明人：KLAUBERT DIETER H; GEE KYLE R
权利人:MOLECULAR PROBES INC
摘要:Facile syntheses for fluorinated resorcinol and aminophenol derivatives are provided that yield isomer-free products in good yield. These novel methods use generally available precursors and standard laboratory reagents and equipment to reproducibly produce these synthetically useful reagents in relatively large quantities. The resulting fluorinated resorcinols and aniinophenols possess utility in the preparation of fluorinated fluorescein and rhodol dyes.

专利号:US-5780603-A
优先权日:1996-11-15
标题:Combinatorial synthesis of carbohydrate libraries
发明人：HINDSGAUL OLE
权利人:SYNSORB BIOTECH INC
摘要:Disclosed are methods for synthesizing very large collections of diverse thiosaccaride derivatives optionally attached to a solid support. Also disclosed are libraries of diverse thiosaccaride derviatives.