CAS: 4695-62-9; (1S,4R)-1,3,3-Trimethylbicyclo[2.2.1]Heptan-2-One

该化合物是一种具有分子式C10H16O的双环单人酮,自然地存在于燃料油和其他基本油类中,其特点是独特的阵状芳香,广泛用于调味和香味应用.作为手工业化合物,(+)-芬琴酮具有高对称纯度,在不对称合成和制药研究中具有价值.其稳定性和低毒性进一步增强了其在有机合成中的适宜性,并成为分析化学的参考标准.该化合物的硬性双周期结构也有利于立体化学和分子模型的研究.

结构式图片

相似化合物

7787-20-4 1195-79-5 1632-73-1

欧盟法规

ECHA物质C&L通报REACH预注册

上下游产品

CAS号512-13-0 溶剂红172 | CAS号4695-62-9 茴香酮 | CAS号7664-93-9 硫酸 | CAS号470-08-6 (-)-beta-fenchol | CAS号7697-37-2 硝酸 | CAS号144-62-7 草酸 | CAS号64-19-7 冰醋酸 | CAS号595-46-0 二甲基丙二酸 | CAS号2051-44-7 is°Camphoronic acid | CAS号77370-41-3 3-methyl-1,2,3-... | CAS号79-31-2 异丁酸 | CAS号535-77-3 间伞花烃 | CAS号499-75-2 香芹酚 | CAS号4695-62-9 茴香酮 | CAS号18368-91-7 葑醇

合成工艺路线路线简述

  • 1195-79-5 = 4695-62-9 + 7787-20-4
    反应条件:1.1
    标题:Study Of Chiral Ionic Liquid As Stationary Phases For Gc
    作者:By Sun,Xiaojie Et Al
    参考文献:Chromatographia 日期:2013 卷标:76(15-16) 页码:1013-1019
📜1,3,3-三甲基二环[2.2.1]庚烷-2-醇置于c44H66O8P4Pd2,丁烯酮体系中,用 水,甲苯 作为反应溶剂,化学反应 16.0H,以86%的收率获得产物(+)-葑酮
参考文献:次膦氧化物作为多配位的配体在醇的化学选择性钯催化氧化中进行.
标题:次膦氧化物作为多配位的配体在醇的化学选择性钯催化氧化中进行.
摘要:通过吸氢方法,仲膦氧化物o = Phr 2(spos)被鉴定为化学选择的pd催化醇氧化的多态预配体.发现spo通过产生推定的活性h-Pd物种来促进氢的吸收步骤以及氢向迈克尔受体的转移.该催化体系在中性条件下运行,并被证明与底物中的各种亲电子和亲核官能团以及对水和空气敏感的官能团兼容.
DOI:10.1002/cctc.201601261

海关参考信息

专利信息


专利号:US-2021206711-A1
优先权日:2020-01-03
标 题:Synthesis of the Grape Mealybug Pheromone trans-alpha-Necrodyl Isobutyrate
发明人:CHEBNY VINCENT JAMES
权利人:TRECE INC
摘要:Methods are provided for synthesizing the grape mealybug pheromone, trans-α-necrodyl isobutyrate, starting with essential plant oils that contain trans-α-necrodyl acetate. The synthesis method, in two steps, converts the trans-α-necrodyl acetate to trans-α-necrodol and then converts the trans-α-necrodol to the desired trans-α-necrodyl isobutyrate. The first step can be achieved by either of a hydrolysis reaction or a reduction reaction. In the hydrolysis reaction, the essential oil is mixed in an alcohol solvent with a hydroxide base, or by mixing the essential oil in an aqueous acid. A reduction reaction can instead by performed in an organic solvent in the presence of a reducing agent. The trans-α-necrodol is converted to the desired trans-α-necrodyl isobutyrate by an esterification reaction with a carboxylic acid, an acyl halide, or an acid anhydride.

专利号:US-5629394-A
优先权日:1992-12-17
标 题 :Direct synthesis by living cationic polymerization of nitrogen-containing polymers
发明人:CHERADAME HERVE M; CHEN FRANK J; STANAT JON E R; NGUYEN HUNG A; TABAR BEHROOZ R
权利人:EXXON CHEMICAL PATENTS INC
摘要:A method is provided for the direct synthesis by living cationic polymerization of novel polymeric materials functionalized with desirable nitrogen-containing functional groups such as terminal azido, cyano, carbonylamino, cyanato, thiocyanato or thiocarbonylamino groups. Polymerization and functionalization occur in a substantially simultaneous manner. All necessary reactants for the functionalization are present when polymerization is initiated. The nitrogen-containing functional group is provided as a part of a molecule having a release moiety which is preferably resonance stabilized or a tertiary alkyl type and which acts to aid the nitrogen-containing species in functioning as a leaving group.

专利号:US-5900227-A
优先权日:1996-06-17
标题 :Multicyclic nitrone spin trapping compositions
发明人:JANZEN EDWARD G; SANKURATRI NAGARAJU
权利人:OKLAHOMA MED RES FOUND
摘要:Multicyclic nitrone spin trapping compounds capable of forming stable free radical spin adducts are provided as well as methods for their synthesis. The multicyclic nitrone spin trapping compounds can be reacted with a free radical, such as a hydroxy or hydroperoxy radical, in solution to form a spin adduct which is stable and readily detectable by electron paramagnetic resonance (EPR) spectroscopy. The multicyclic nitrone spin traps can be used to detect free radicals in a sample such as a biological system. In one embodiment, the spin trapping compound, 1,3,3-trimethyl-6-azabicyclo-[3.2.1]oct-6-ene-N-oxide ('TRAZON') is provided, as well as methods for the synthesis of TRAZON and of modified forms of TRAZON. TRAZON can react with a wide range of different free radicals in solution to form free radical spin adducts which are readily detectable by EPR.

专利号:EP-3628658-A1
优先权日:2018-09-28
标 题:Synthesis of substituted enones

专利号:DE-102015224955-A1
优先权日:2015-12-11
标 题 :Synthesis of ketone-releasing photocages

专利号:PL-114672-B1
优先权日:1978-02-17
标 题:Process for purification of fenchone obtained from wastes from synthesis of borneols from alpha-pinene

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

[参考文献]: Uzi Ravid, Et Al. Chiral Gc Analysis Of Enantiomerically Pure Fenchone In Essential Oils.
[参考文献]: Antonio A Ceacero-Vega, Et Al. Kinetics And Mechanisms Of The Tropospheric Reactions Of Menthol, Borneol, Fenchol, Camphor, And Fenchone With Hydroxyl Radicals (Oh) And Chlorine Atoms (Cl). J Phys Chem A. 2012 Apr 26;116(16):4097-107.
[参考文献]: Boris Steuer, Et Al. Near-Infrared Analysis Of Fennel (Foeniculum Vulgare Miller) On Different Spectrometers--Basic Considerations For A Reliable Network. Phytochem Anal. 2003 Sep-Oct;14(5):285-9.
[参考文献]: Dirk W Lachenmeier, Et Al. Long-Term Stability Of Thujone, Fenchone, And Pinocamphone In Vintage Preban Absinthe. J Agric Food Chem. 2009 Apr 8;57(7):2782-5.
[参考文献]: M Bjan, Et Al. [参考文献]: Rev Med Chir Soc Med Nat Iasi. 2011 Apr-Jun;115(2):590-4.

合成参考文献


摘要:Toyota, S.; Iwanaga, T., Science of Synthesis, (2010) 45, 802.
摘要:Food and Cosmetics Toxicology., 2(327), 1964
摘要:Schafer, E. W., Jr., W. A. Bowles Jr., and J. Hurlbut. 1983. The acute oral toxicity and repellency and hazard potential of 998 chemicals to one or more species of wild and domestic birds. Archives of Environmental Contamination and Toxicology 12:355-382. https://www.aphis.usda.gov/ws/nwrc/chem-effects-db/Q_schafer832.pdf
📝 需求与反馈
尽可能描述清楚需求与问题信息
×

通知