CAS: 1113-21-9; (E,E)-3,7,11,15-Tetramethyl-1,6,10,14-Hexadecatetraen-3-Ol

该化合物是一种天然有机化合物,被归类为二乙醇,其特点是长碳链,由20个碳原子和多个双环组成,造成其不饱和性.Phytol一般是无色的,可粉黄的,可粉色的,有温和的,草味的液体.它溶于有机溶剂中,但因其缺水特性,溶解于水中溶解性有限.该化合物在维生素E和叶绿素的生物合成中起到显著作用,在各种生物工艺中起到先导作用.Phytol表现出抗氧化性特性,在红和口工业以及某些药品的生产中具有应用作用.此外,它还被用于对Retinol(vitmin A)的合成,并具有潜在的治疗作用,因此它既具有营养和医药化学两个方面都具有意义.

结构式图片

相似化合物

68931-30-6 7212-44-4 40716-66-3

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593-60-2 溴乙烯 | CAS号1117-52-8 法尼基丙酮 | CAS号3796-70-1 香叶基丙酮 | CAS号59905-15-6 3-hydroxy-3,7,1... | CAS号21064-19-7 三甲基-1,5,9-环十二碳三烯 | CAS号63525-04-2 4,8-dimethyl-12... | CAS号24034-73-9 香叶基香叶醇 | CAS号6809-52-5 替普瑞酮 | CAS号67979-80-0 15,19,23-trimet... | CAS号89503-33-3 6,10,14,18-tetr... | CAS号50848-64-1 geranyl geranyl... | CAS号80321-08-0 (2Z,6E,10E)-1-b... | CAS号62235-06-7 (3E,7E)-4,8,12-... | CAS号3796-64-3 (E,E,E)-geranyl... | CAS号3796-63-2 (5E,9E,13E)-Tep...

合成工艺路线路线简述

  • 合成目标产物 Geranyl Linalool 主要起始原料 (5E,9E)-6,10,14-Trimethylpentadeca-5,9,13-Trien-2-One And Vinyl Lithium
  • (文献来源)合成步骤主要原料 (5E,9E)-6,10,14-Trimethylpentadeca-5,9,13-Trien-2-One 和 Vinyl Lithium

海关参考信息

专利信息


专利号:US-4061660-A
优先权日:1975-09-29
标 题 :Process for synthesis of coenzyme Q compounds
发明人:KIJIMA SHIZUMASA; YAMATSU ISAO; MINAMI NORIO; INAI YUICHI
权利人:EISAI CO LTD
摘要:A process for the synthesis of 2,3-dimethoxy-5-methyl-6-substituted-1,4-benzoquinones having the formula: ##STR1## wherein R is ##STR2## in which n is an integer of 0 to 9, and A and B are hydrogens or A--B is a direct valence bond between the carbon atoms to which they are attached, n Characterized by reacting 2-methyl-4,5,6-trimethoxyphenol with an aryl boronic acid, a lower alkyl boronic acid or an acid anhydride thereof to obtain a 2-methyl-4,5,6-trimethoxyphenol ester of boric acid, reacting the resulting ester with an n-prenol or iso-prenol having the formula: ##STR3## wherein R is as defined above, OR A REACTIVE DERIVATIVE OF SAID N- OR ISO-PRENOL, IN THE PRESENCE OF A SILICA-ALUMINA COMPOUND, TO OBTAIN A 2-METHYL-3-SUBSTITUTED-4,5,6-TRIMETHOXYPHENOL ESTER OF BORIC ACID, AND HYDROLYZING THE THUS-OBTAINED ESTER AND TREATING THE RESULTING 2-METHYL-3-SUBSTITUTED-4,5,6-TRIMETHOXYPHENOL HAVING THE FORMULA: ##STR4## wherein R is as defined above, WITH AN OXIDIZING AGENT.

专利号:US-2024228454-A1
优先权日:2021-04-28
标 题 :Ring closure of benzoquinones containing an unsaturated side chain using a base in two-phase system
发明人:BONRATH WERNER; KUENZI ROLF
权利人:DSM IP ASSETS BV
摘要:The present invention relates to the formation of compound of the formula (I) by a ring closure reaction of the compound of the formula (II) in the presence of a base in a two-phase system. It has been found that this reaction is very efficient and offers for example an efficient pathway for the synthesis of 3,4-dehydro-α-tocotrienol respectively a-tocotrienol and a-tocopherol.

专利号:US-4062879-A
优先权日:1975-09-29
标 题 :Process for synthesis of coenzyme Q compounds
发明人:KIJIMA SHIZUMASA; YAMATSU ISAO; MINAMI NORIO; INAI YUICHI
权利人:EISAI CO LTD
摘要:A process for synthesizing 2,3-dimethoxy-5-methyl-6-substituted-1,4-benzoquinones having the formula: ##STR1## wherein R is ##STR2## in which n is an integer of 0 to 9, and A and B are hydrogens or taken together form a valence bond, n In which 2-methyl-4,5,6-trimethoxyphenol is reacted with boric acid or a reactive derivative thereof to obtain a 2-methyl-4,5,6-trimethoxyphenol ester of boric acid, reacting the resulting ester with an n-prenol or iso-prenol having the formula: ##STR3## wherein R is as defined above, OR A REACTIVE DERIVATIVE OF SAID N- OR ISO-PRENOL, IN THE PRESENCE OF A SILICA-ALUMINA COMPOUND, TO OBTAIN A 2-METHYL-3-SUBSTITUTED-4,5,6-TRIMETHOXYPHENOL ESTER OF BORIC ACID, AND HYDROLYZING THE THUS-OBTAINED ESTER AND TREATING THE RESULTING 2-METHYL-3-SUBSTITUTED 4,5,6-TRIMETHOXYPHENOL HAVING THE FORMULA: ##STR4## wherein R is as defined above, with an oxidant.

专利号:US-2004249219-A1
优先权日:2000-07-05
标题 :Method of making teprenone
发明人:SAUCY GABRIEL G
摘要:The invention is directed to an efficient and economical method of making teprenone. Teprenone is synthesized by converting geranylgeraniol to teprenone by a novel route. The method of synthesis can begin with geranylgeraniol obtained from a biological source such as fermentation of a microorganism capable of producing geranylgeranyl or enzymatic synthesis in a cell free system to produce predominantly the 5E isomer of teprenone. The chemical synthesis proceeds with retention of configuration such that the teprenone produced has the isomeric configuration of the geranylgeraniol starting material.

专利号:CN-105647896-A
优先权日:2016-02-04
标题 :A protein related to the synthesis of terpenes and its application

专利号:CN-105647897-B
优先权日:2016-02-04
标题:A protein related to the synthesis of terpenes and its application
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合成参考文献


摘要:Singh, F. V.; Wirth, T., Science of Synthesis Knowledge Updates, (2015) 2, 418.
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