CAS: 1120-06-5; 2-Decanol

上下游产品

1,2-Epoxydecane ethanol °Ct-1-ene di-tert-butyl peroxide Valeriansaeure-2-decanester 2-Trimethylsilyloxy-decan 1-methylnonyl stearate (3,5-Dinitro-phenyl)-carbamic acid (R)-1-methyl-nonyl ester Alcohols ( 1,10-decanedioic acid trans-3-decen-5-yn-2-one dec-3-en-2-one 1-Decene decane decan-2-ol (+/-)-2-Amino-decan 1-phenyl-1-undecen-3-one Ketones ( o-fluorophenylmercuric chloride 2-fluorothiophenol 1-Fluoro-2-iodobenzene 2-fluorobenzenediazonium tetrafluoroborate 2-(2-fluoro-phenylsulfanyl)-4-trifluoromethoxy-benzaldehyde (S)-1-{4-[2-(2-Fluoro-benzenesulfonyl)-4-trifluoromethoxy-benzyl]-phenyl}-ethylamine N-(1-{4-[2-(2-fluoro-benzenesulfonyl)-4-trifluoromethoxy-benzoyl]-phenyl}-ethyl)-methanesulfonamideN-(1-{4-[2-(2-fluoro-benzenesulfonyl)-4-trifluoromethoxy-benzoyl]-phenyl}-ethyl)-methanesulfonamide N-(1-{4-[2-(2-fluoro-phenylsulfanyl)-4-trifluoromethoxy-benzyl]-phenyl}-ethyl)-acetamide2,2,2-trifluoro-N-(1-{4-[2-(2-fluoro-phenylsulfanyl)-4-trifluoromethoxy-benzyl]-phenyl}-ethyl)-acetamide

📜2-癸酮置于palladium On Activated Charcoal 水,氢气体系中,化学反应 72.0H,反应生成2-癸醇
参考文献:氢化条件下脂族仲醇与酮之间新型pd / C催化的氧化还原反应:在h-D交换反应中的应用及机理研究
标题:氢化条件下脂族仲醇与酮之间新型pd / C催化的氧化还原反应:在h-D交换反应中的应用及机理研究
摘要:描述了仲醇和酮之间的液相氧化还原系统.使用pd / Ch 2-D 2 O系统对仲醇或酮进行氘化,得到氘标记的仲醇和酮的混合物.结果表明,在氢化条件下,仲醇在没有氧化剂的情况下被氧化为相应的酮,并且脂肪族酮同时氢化为相应的仲醇.讨论了有关氧化还原系统以及h-D交换反应的详细机理研究.
Doi:10.1021/jo062582U

专利信息

专利号:WO-2014108526-A1
优先权日:2013-01-11
标题 :Synthetic process for the manufacture of pipecolidepsin compounds
发明人：PELAY GIMENO MARTA; GARCÃ?A-RAMOS YESICA; TULLA PUCHE JUDIT; ALBERICIO PALOMERA FERNANDO; MARTÃ?N LÓPEZ M JES S
权利人:PHARMA MAR SA
摘要:(I) wherein R 1 , R 2 , R 3 , R 4 , R 5 , R 6 , R 7 , R 8 , R 9 , R 10 , R 11 , R 12 , n and Y are as described. The invention provides a process for the synthesis of complex pipecolidepsin and related compounds of formula (I), opening a new field of compounds with useful biological properties. The invention also provides intermediates, useful in the synthesis of compounds of formula (I).

专利号:US-9790206-B2
优先权日:2013-02-27
标 题:Intermediates for use in the preparation of indazole derivatives and processes for the preparation thereof
发明人：EARY C TODD; HACHE BRUNO P; JUENGST DERRICK; SPENCER STACEY RENEE; STENGEL PETER J; WATSON DANIEL JOHN
权利人:ARRAY BIOPHARMA INC
摘要:Provided herein are novel processes for preparing a compound of Formula (I) to the use of said compound as an intermediate in novel processes for the synthesis of indazole derivatives, and to indazole intermediates and derivatives prepared by the processes described herein.

专利号:US-5637757-A
优先权日:1995-04-11
标 题 :One-pot synthesis of ring-brominated benzoate compounds
发明人：HILL JOHN E; FAVSTRITSKY NICOLAI A; MAMUZIC RASTKO I; BHATTACHARYA BHABATOSH
权利人:GREAT LAKES CHEMICAL CORP
摘要:A method of preparing tetrabromobenzoate compounds from tetrabromophthalic anhydride by reacting tetrabromophthalic anhydride with alcohol in the presence of a decarboxylation catalyst. The reaction may be carried out in an excess of alcohol, or with a near stoichiometric amount of alcohol by performing the reaction in an inert solvent.

专利号:WO-2012163936-A1
优先权日:2011-05-31
标 题 :Process for the synthesis of benzotriazoles useful as uv-filters
发明人：PRESCHEL MICHAEL; ROEDER MICHAEL; SCHLIFKE-POSCHALKO ALEXANDER; ZHANG KESHENG
权利人:DSM IP ASSETS BV; PRESCHEL MICHAEL; ROEDER MICHAEL; SCHLIFKE-POSCHALKO ALEXANDER; ZHANG KESHENG
摘要:The invention relates to an improved process for the manufacture of novel benzotriazoles as well to novel benzotriazoles obtained by the novel process. This novel economical process provides products in high purity and yields.

专利号:US-8329854-B2
优先权日:2010-09-27
标题 :Synthesis of tri-component resins
发明人：BIRAU MARIA; ALLEN C GEOFFREY
权利人:BIRAU MARIA; ALLEN C GEOFFREY; XEROX CORP
摘要:A resinous compound of the formulas or a salt thereof, wherein G1 is —X1C(O)OR1, —X2OC(O)R2, or —X2OH; G2 is R4, R12, —C(O)R2, —C(O)X1C(O)OR1, or —C(O)X2OC(O)R2; R1 is an alkyl having from 10 to 80 carbon atoms; R2 is an alkyl having from 2 to 40 carbon atoms; each R3 and R4 is independently hydrogen, alkyl, arylalkyl or alkylaryl; each R5 and each R6 is independently hydrogen or alkyl; X1 and X2 are both a straight or branched alkylene group; t1 is 1 to 20; t2 and t3 is independently 0 to 20; u1 is 1 to 30; u2 and u3 is independently 0 to 30; each R7 and each R8 is independently hydrogen, alkyl, or alkoxyl; each R9 and each R10 is independently hydrogen, alkyl, or alkoxyl; Ar is a substituted or unsubstituted aromatic moiety; p is 1 to 5; q is 1 to 12; A⊖ is selected from the group consisting of Cl−, Br−, I−, HSO4−, HSO3−, CH3SO3−, NO3−, HCOO−, CH3COO−, H2PO4−, SCN−, BF4−, ClO4−, SSO3−, PF6−, and SbCl6−; and J is alkyl, arylalkyl, or alkylaryl.

专利号:US-10017465-B2
优先权日:2014-08-12
标 题 :Method for producing astaxanthin from astacin
发明人：Schäfer Bernd; SIEGEL WOLFGANG
权利人:BASF SE
摘要:The invention relates to a method for the non-stereoselective and also for the stereoselective synthesis of astaxanthin from astacin. For this purpose, a reducing agent is used selected from the group of hydrogen, a secondary alcohol, formic acid and also the salts of formic acid or from a mixture of at least two representatives of the compound classes stated above. The invention further relates to the use of astacin as starting compound for the synthesis of astaxanthin.