CAS: 18409-18-2; (E)-Dec-2-En-1-Ol

该化合物是含有分子式C10H20O的不饱和脂肪酒精,该化合物在2位置和一个主要氢氧基组中具有跨形双重结合,有助于其在有机合成中的回作用和实用性,是生产香味,口味和特殊化学品的关键中间体,因其独特结构而成为生产香味,口味和特殊化学品的关键中间体.这种反配置可增强稳定性并影响其物理化学特性,如熔点和溶解性.其纯度和界定的立体化学特性使得它对于需要精确分子控制的研究和工业应用具有价值,需要精确的分子控制.适合在标准实验室条件下以适当处理的方式使用.

结构式图片

欧盟法规

ECHA物质C&L通报REACH预注册

上下游产品

CAS号7367-88-6 反-2-癸烯酸乙酯 | CAS号4117-14-0 2-癸炔-1-醇 | CAS号3913-81-3 反式-2-癸烯醛 | CAS号1219000-89-1 (E)-1-(methoxym... | CAS号69814-31-9 2-(phenylseleno... | CAS号124-13-0 正辛醛 | CAS号867-13-0 磷酰基乙酸三乙酯 | CAS号84988-53-4 (E)-2-decenyl c... | CAS号70719-29-8 2-benzenesulfin... | CAS号629-04-9 1-溴庚烷 | CAS号3913-81-3 反式-2-癸烯醛 | CAS号14167-87-4 decyl diphenyl ... | CAS号872-05-9 正癸烯 | CAS号112-17-4 乙酸癸酯 | CAS号20063-97-2 2-Decene, (E) | CAS号2497-23-6 dec-2-enyl acetate | CAS号112-31-2 癸醛 | CAS号112-30-1 正癸醇 | CAS号13151-28-5 3-methyldec-1-ene | CAS号24738-51-0 DODECA-2(E),4(E...

合成工艺路线路线简述

  • 合成目标产物 Trans-2-Decen-1-Ol 主要起始原料 Octanal
  • (文献来源)合成步骤主要原料 Octanal
📜Heptylmagnesium Bromide置于吡啶,乙醚,Sodium Acetate,三溴化磷,溶剂黄146体系中,化学反应生成反式-2-癸烯醇
参考文献:Delaby,Bulletin De La Societe Chimique De France,1936,Vol. <5>3,P. 2380
标题:Delaby,Bulletin De La Societe Chimique De France,1936,Vol. <5>3,P. 2380

海关参考信息

专利信息


专利号:US-8865624-B2
优先权日:2010-09-01
标题 :Inhibitor for tobacco axillary bud growth and method for inhibiting tobacco axillary bud growth
发明人:TANAKA MOTOKI; TANAKA KEIJITSU; SHIBUYA TAKESHI; IKUTA EIJI; YOSHINAGA KOTARO; YAMAGUCHI YUKI
权利人:TANAKA MOTOKI; TANAKA KEIJITSU; SHIBUYA TAKESHI; IKUTA EIJI; YOSHINAGA KOTARO; YAMAGUCHI YUKI; SDS BIOTECH CORP
摘要:The present invention relates to an inhibitor for tobacco axillary bud growth, the inhibitor comprising, as an active ingredient, one or more kinds of very-long chain fatty acid synthesis inhibitors such as a chloroacetamide-based herbicide, fentrazamide, cafenstrole or indanofan; an inhibitor for tobacco axillary bud growth, the inhibitor comprising the aforesaid very-long chain fatty acid synthesis inhibitor together with clorthal-dimethyl or an aliphatic alcohol having 6 to 20 carbon atoms; and a method for inhibiting tobacco axillary bud growth which comprises applying the inhibitor for tobacco axillary bud growth. The inhibitor for tobacco axillary bud growth of the present invention shows sustained drug efficacy at a low concentration, induces neither chemical injury nor disease, and can contribute to the improvement in labor productivity.

专利号:US-8859615-B2
优先权日:2008-08-27
标题 :Compounds, compositions and methods for reducing toxicity and treating or preventing diseases
发明人:DANISHEFSKY SAMUEL J; CHOU TING-CHAO; LEI XIAOGUANG; YUN HEEDONG; NG FAY; HARTUNG JOHN; SAMES DALIBOR
权利人:DANISHEFSKY SAMUEL J; CHOU TING-CHAO; LEI XIAOGUANG; YUN HEEDONG; NG FAY; HARTUNG JOHN; SAMES DALIBOR
摘要:The present invention provides compounds of Formula (I), compositions comprising an effective amount of a compound of Formula (I), optionally with chemotherapeutic drugs such as a tubulin-binding drug, and methods of their use for reducing the toxicity of cytotoxic agents, treating or preventing cancer or a neuropathic disorder, inducing a chemoprotective phase II enzyme, DNA, or protein synthesis, enhancing the immune system, treating inflammation, improving and enhancing general health or well-being, and methods for making compounds of Formula (I).

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

参考标题:Convergent Synthesis Of Calcium-Dependent Antibiotic Cda3A And Analogues With Improved Antibacterial Activity Via Late-Stage Serine Ligation
作者:Delin Chen,Kathy Hiu Laam Po,Pilar Blasco,Sheng Chen,Xuechen Li |发布日期:2020.6.19
摘要:A Convergent Synthesis Via The Late-Stage Serine Ligation Of Naturally Occurring Calcium-Dependent Antibiotic Cda3A And Its Analogues Has Been Developed, Which Allowed Us To Readily Synthesize The Analogues With The Variation On The Lipid Tail. Some Analogues Were Found To Show 100-500-Fold Higher Antimicrobial Activity Than The Natural Compound Cda3A Against Drug Resistant Bacteria. This Study Will

合成参考文献


摘要:Race, N. J.; Patel, H. H.; Sigman, M. S., Science of Synthesis: Catalytic Oxidation in Organic Synthesis, (2017) 1, 445.
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