CAS: 119-13-1; (R)-2,8-Dimethyl-2-((4R,8R)-4,8,12-Trimethyltridecyl)Chroman-6-Ol

该化合物是一种高纯度的氯酚异构体,主要因其抗氧化特性和富脂环境中的稳定性而得到承认.作为维生素E家族的天然成分,它比合成替代品更能耐氧化性降解.它的高度浓度(>90%)确保了在需要强力氧化性保护的应用(如食品保存,化妆品和药品)方面始终如一的性能.-多氯酚特别有效抑制脂过氧化性,使其在易腐化的配方中具有价值.该化合物是脂质溶性,便于融入以石油为基础的系统.其非基因改变和植物来源的成分进一步增强了其对清洁标签和天然产品配方的适宜性.

结构式图片

欧盟法规

REACH注册ECHA物质C&L通报REACH预注册

上下游产品

CAS号71528-84-2 4-hydroxy-3-met... | CAS号150-86-7 植物醇 | CAS号95-71-6 鹿蹄草素 | CAS号67289-05-8 1,4-Benzenediol... | CAS号408340-52-3 Acetic acid, [(... | CAS号108127-42-0 6-hydroxy-7-met... | CAS号5307-05-1 2-甲基-4-甲氧基苯酚 | CAS号54-28-4 (+)-gamma-生育酚 | CAS号59-02-9 维生素E油 | CAS号4345-03-3 维生素E琥珀酸酯 | CAS号2668-47-5 2,6-ditert-buty... | CAS号34004-56-3 δ-chromanoxyl r... | CAS号766-07-4 cyclohexyl hydr... | CAS号119-13-1 (+)-Delta-生育酚 | CAS号6257-38-1 2,6-ditert-buty...

合成工艺路线路线简述

  • 合成目标产物 D-Delta-Tocopherol 主要起始原料 Ethanamine, N-[(3,5-Dichlorophenyl)Methylene]-2,2-Diethoxy-
  • (文献来源)合成步骤主要原料 Ethanamine, N-[(3,5-Dichlorophenyl)Methylene]-2,2-Diethoxy-
📜6-Phytyltoluquinol置于tocopherol Cyclase From Spheroplasts Of Anabaena Variabilis体系中,用 丙酮 用作溶剂,化学反应生成(+)-δ-生育酚
参考文献:The Substrate Specificity Of Tocopherol Cyclase
标题:The Substrate Specificity Of Tocopherol Cyclase
摘要:The Substrate Specificity Of The Enzyme Tocopherol Cyclase From The Blue-Green Algae Anabaena Variabilis (Cyanobacteria) Was Investigated With 11 Substrate Analogues Revealing The Significance Of Three Major Recognition Sites: (I) The Oh Group At C(1) Of The Hydroquinone,(II) The (E) Configuration Of The Double Bond,And (III) The Length Of The Lipophilic Side Chain. Experiments With Two Affinity Matrices Suggest That Substrates Approach The Enzyme'S Active Site With The Hydrophobic Tail. Copyright (C) 1996 Elsevier Science Ltd
Doi:10.1016/0968-0896(96)00125-3

海关参考信息

专利信息


专利号:US-7435861-B2
优先权日:2005-04-29
标 题 :Methods for synthesis of carotenoids, including analogs, derivatives, and synthetic and biological intermediates
发明人:LOCKWOOD SAMUEL F; TANG PENG CHO; NADOLSKI GEOFF; JACKSON HENRY L; FANG ZHIQIANG; DU YISHU; YANG MIN; GEISS WILLIAM; WILLIAMS RICHARD; BURDICK DAVID
权利人:CARDAX PHARMACEUTICALS INC
摘要:A method for synthesizing intermediates for use in the synthesis of carotenoid synthetic intermediates, carotenoid analogs, and/or carotenoid derivatives. The carotenoid analog, derivative, or intermediate may be administered to a subject for the inhibition and/or amelioration of any disease that involves production of reactive oxygen species, reactive nitrogen species, radicals and/or non-radicals. In some embodiments, the invention may include methods for synthesizing chemical compounds including an analog or derivative of a carotenoid. Carotenoid analogs or derivatives may include acyclic end groups. In some embodiments, a carotenoid analog or derivative may include at least one substituent. The substituent may enhance the solubility of the carotenoid analog or derivative such that the carotenoid analog or derivative at least partially dissolves in water.

专利号:US-2008221377-A1
优先权日:2006-06-16
标题 :Methods for synthesis of carotenoids, including analogs, derivatives, and synthetic and biological intermediates
发明人:LOCKWOOD SAMUEL F; TANG PENG CHO; NADOLSKI GEOFF; JACKSON HENRY L; FANG ZHIQIANG; DU YISHU; YANG MIN; GEISS WILLIAM; WILLIAMS RICHARD; BURDICK DAVID; BRAUN CRISTI L
权利人:LOCKWOOD SAMUEL F; TANG PENG CHO; NADOLSKI GEOFF; JACKSON HENRY L; FANG ZHIQIANG; DU YISHU; YANG MIN; GEISS WILLIAM; WILLIAMS RICHARD; BURDICK DAVID; BRAUN CRISTI L
摘要:A method for synthesizing intermediates for use in the synthesis of carotenoid synthetic intermediates, carotenoid analogs, and/or carotenoid derivatives. The carotenoid analog, derivative, or intermediate may be administered to a subject for the inhibition and/or amelioration of any disease that involves production of reactive oxygen species, reactive nitrogen species, radicals and/or non-radicals. In some embodiments, the invention may include methods for synthesizing chemical compounds including an analog or derivative of a carotenoid. Carotenoid analogs or derivatives may include acyclic end groups. In some embodiments, a carotenoid analog or derivative may include at least one substituent. The substituent may enhance the solubility of the carotenoid analog or derivative such that the carotenoid analog or derivative at least partially dissolves in water.

专利号:US-2024132430-A1
优先权日:2021-08-05
标 题 :Chemicals and use of hypohalites in mechanism-based selective dual radical organic synthesis
发明人:PALOMINO EDUARDO
权利人:WALKER CANCER RES INSTITUTE INC
摘要:The synthesis of pattern-specific compounds using hypohalites, such as hypochlorous acid, sodium hypochlorite, and potassium hypoiodite, as dual-radical generators is provided. The synthesis can be implemented by a cyclization reaction, a dehydrogenation reaction, a hydroxylation reaction, a decarboxylation reaction, or any combination of the above four. The reactions are typically carried out in water, in a nonpolar solvent such as ethyl acetate, or a mixture of both. Hypochlorous acid is made by adding a weak acid such as acetic acid to sodium hypochlorite.

专利号:US-9981935-B2
优先权日:2013-07-05
标 题:Formation of chiral 4-chromanones using chiral pyrrolidines in the presence of acids
发明人:MEDLOCK JONATHAN ALAN; LETINOIS ULLA; NETSCHER THOMAS; BONRATH WERNER
权利人:DSM IP ASSETS BV
摘要:The present invention relates to a synthesis of chromanones or chromanes in a stereospecific matter in view of the 2-position in the chromanone or chromane ring. It has been found that this synthesis is particularly possible in the presence of a chiral compound of a specific type and of at least one Bransted acid or in the presence a specific chiral compound having a Bransted acid functional group in the molecule.

专利号:US-8703812-B2
优先权日:2005-07-29
标 题 :Protein synthesis required for long-term memory is induced by PKC activation on days preceding associative learning
发明人:ALKON DANIEL L
权利人:ALKON DANIEL L; BRNI NEUROSCIENCES INST
摘要:The present invention provides methods of contacting a protein kinase C (PKC) activator with a PKC activator in a manner sufficient to stimulate the synthesis of proteins sufficient to consolidate long-term memory. The present invention also provides methods of contacting a protein kinase C (PKC) activator with a PKC activator in a manner sufficient to downregulate PKC.

专利号:US-9815809-B2
优先权日:2013-07-05
标题:Formation of chiral 4-chromanones using chiral pyrrolidines in the presence of phenols or thiophenols
发明人:LETINOIS ULLA; NETSCHER THOMAS
权利人:DSM IP ASSETS BV
摘要:The present invention relates to a synthesis of chromanones or chromanes in a stereospecific matter in view of the 2-position in the chromanone or chromane ring. It has been found that this synthesis is particularly possible in the presence of a chiral compound of formula of a specific type and of at least one phenol or thiophenol.

供应商参考报价(招募中)

品牌试剂参考报价(招募中)

📌 第三方产品分析报告

✅ COA系统入驻 | 共享模式

主要参考文献


1: Kamei Y, Otsuka Y, Abe K. Comparison of the inhibitory effects of vitamin E analogues on melanogenesis in mouse B16 melanoma cells. Cytotechnology. 2009 Apr;59(3):183-90. doi: 10.1007/s10616-009-9207-y. Epub 2009 Jul 1.
2: Kelly MJ, Mathie AZ, Vallance C. A pharmacological action of vitamin E unrelated to its antioxidant capacity. Methods Find Exp Clin Pharmacol. 2006 Oct;28(8):499-505. doi: 10.1358/mf.2006.28.8.1003577. 80(3):611-21. 25(1):40-8. 107(12):2236-43. doi: 10.1093/jn/107.12.2236.

合成参考文献


参考文献:10.1016/j.jnutbio.2011.03.003
摘要:Wang Y, Moreland M, Wagner JG, Ames BN, Illek B, Peden DB, Jiang Q. Vitamin E forms inhibit IL-13/STAT6-induced eotaxin-3 secretion by up-regulation of PAR4, an endogenous inhibitor of atypical PKC in human lung epithelial cells. The Journal of Nutritional Biochemistry. 2012 Jun;23(6):602–8. doi: 10.1016/j.jnutbio.2011.03.003.
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