CAS: 21020-27-9; 4-Methylpent-2-Yne

该化合物是一种烷,具体地说是一种终端烷,其特点是碳原子之间的三联;其分子分子式C6H10,表明含有6个碳原子和10个氢原子;该化合物具有一个分支结构,其甲基组附于5碳链的第四碳,其中包括第二和第三碳之间的三联. 4-甲基-2-苯是一种无色液体,在室温下是无色液体,以其独特的气味而著称.它相对非极化,在有机溶剂中溶解,但在水中则较少溶解.该化合物是易燃的,应谨慎处理,因为它可能构成与烷再活性相关的危害,包括在某些情况下潜在的聚合.其应用可能包括作为有机合成的中间体和生产各种化学化合物.在与该物质打交道时,由于易燃性和潜在的健康风险,应当注意适当的安全措施.

结构式图片

欧盟法规

ECHA物质C&L通报

上下游产品

CAS号590-38-5 2-甲基-3-戊炔-2-醇 | CAS号115-11-7 2-甲基丙烯 | CAS号999-79-1 2-Pentyne, 4-ch... | CAS号3664-56-0 1,3,3-Trimethyl... | CAS号74866-69-6 (Z)-1-((4-methy... | CAS号691-38-3 顺式-4-甲基-2-戊烯 | CAS号57497-10-6 1-bromo-2,3-dim... | CAS号108-10-1 甲基异丁基甲酮 | CAS号565-69-5 2-甲基-3-戊酮 | CAS号108-10-1 甲基异丁基甲酮 | CAS号691-38-3 顺式-4-甲基-2-戊烯 | CAS号31151-19-6 1H-Indole,2-met... | CAS号91639-44-0 1H-Indole,3-met... | CAS号80213-80-5 5-methoxy-2-met... | CAS号80213-79-2 5-methoxy-3-met... | CAS号825622-15-9 6-methylhept-3-... | CAS号4461-48-7 4-甲基-2-戊烯(顺反异构体混和物)

合成工艺路线路线简述

  • 合成目标产物 4-Methyl-2-Pentyne 主要起始原料 2-Methyl-3-Pentyn-2-Ol
  • (文献来源)合成步骤主要原料 2-Methyl-3-Pentyn-2-Ol
📜顺式-4-甲基-2-戊烯置于溴,甲基环己烷体系中,化学反应生成甲基異丙基乙炔
参考文献:Mono-And Di-Alkylacetylenes From Vicinal Dihalides And Sodium Amide In Liquid Ammonia1
标题:Mono-And Di-Alkylacetylenes From Vicinal Dihalides And Sodium Amide In Liquid Ammonia1
摘要:
Doi:10.1021/jo01377A003

海关参考信息

专利信息


专利号:WO-2012088402-A1
优先权日:2010-12-22
标题 :Synthesis of conolidine and discovery of a potent non-opioid analgesic for pain
发明人:BOHN LAURA M; MICALIZIO GLENN C
权利人:SCRIPPS RESEARCH INST; BOHN LAURA M; MICALIZIO GLENN C
摘要:The first de novo synthetic pathway to the exceptionally rare C5-nor stemmadenine natural product, conolidine, and the first asymmetric synthesis of any member of this natural product class arc described. C5-nor stemmadenine compositions are also described. These compounds, for example,(+/- )-,(+)- and (-)-conolidine are potent and efficacious non-opioid analgesics in tonic and persistent pain.

专利号:US-7632975-B2
优先权日:2004-12-22
标 题:Process for the synthesis of arylfluorenes and analogs thereof
发明人:HEIDENHAIN SOPHIE
权利人:CDT OXFORD LTD
摘要:A process is provided for the synthesis of a compound of formula (I): n nwherein:n M=0 or 1; N and p are 0 or 1 to 4; X is a single bond, O, S or NH; And R 1 -R 4 are as defined in claim 1.

专利号:US-10570114-B2
优先权日:2016-05-19
标题:Synthesis of 6-aryl-4-aminopicolinates and 2-aryl-6-aminopyrimidine-4-carboxylates by direct suzuki coupling
发明人:FISK JASON S; LI XIAOYONG; Muehlfeld Mark; BAUMAN ROBERT S; OPPENHEIMER JOSSIAN; TU SIYU; NITZ MARK A; CHAKRABARTI REETAM; FEIST SHAWN D; RINGER JAMES W; LENG RONALD B
权利人:DOW AGROSCIENCES LLC
摘要:Improved methods of synthesizing 6-aryl-4-aminopicolinates, such as arylalkyl and alkyl 4-amino-3-chloro-6-(4-chloro-2-fluoro-3-methoxyphenyl)pyridine-2-carboxylates and arylalkyl and alkyl 4-amino-3-chloro-5-fluoro-6-(4-chloro-2-fluoro-3-methoxyphenyl)pyridine-2-carboxylates, are described herein. The improved methods include a direct Suzuki coupling step, which eliminates the protection/de-protection steps in the current chemical process, and therefore eliminates or reduces various raw materials, equipment and cycle time as well as modification of other process conditions including use of crude AP, use of ABA-diMe, and varying pH, catalyst concentration, solvent composition, and/or workup procedures. This includes synthesis of 2-aryl-6-aminopyrimidine-4-carboxylates.

专利号:US-2013184465-A1
优先权日:2010-09-30
标 题:Process for the synthesis of thio-triazolo-group containing compounds
发明人:DOCHNAHL MAXIMILIAN; KEIL MICHAEL; GEBHARDT JOACHIM; VOGELBACHER UWE JOSEF; RACK MICHAEL
权利人:DOCHNAHL MAXIMILIAN; KEIL MICHAEL; GEBHARDT JOACHIM; VOGELBACHER UWE JOSEF; RACK MICHAEL; BASF SE
摘要:The present invention relates to a process using specific magnesium reagents for providing thio-triazolo group-containing compounds and for the synthesis of precursors therefor. The invention furthermore relates to intermediates and to their preparation.

专利号:US-2025188104-A1
优先权日:2023-12-06
标题 :Sequential One-Pot Synthesis of Alkylidyne and Alkylidene Catalysts
发明人:VEIGE ADAM S; BOECK PARK
权利人:THE UNIV OF FLORIDA RESEARCH FOUNDATION INC
摘要:A method of preparing a tetraanionic pincer ligand supported metallacycloalkylene complex in one pot, the method including admixing at low temperature a solution of [ t BuOCO]H 3 and a solution of ( t BuO) 3 W≡CC(CH 3 ) 3 in a second solvent to form a first reaction mixture, warming the first reaction mixture, removing at least a portion of solvent from the first reaction mixture to provide a second reaction mixture, admixing the second reaction mixture and a solvent to form a third reaction mixture, admixing at low temperature the third reaction mixture and a base to form a fourth reaction mixture, warming the fourth reaction mixture to form a fifth reaction mixture; removing at least a portion of the third solvent from the fifth reaction mixture to provide a sixth reaction mixture; washing the sixth reaction mixture with a fifth solvent and removing at least a portion of the fifth solvent to form a seventh reaction mixture; admixing the seventh reaction mixture with a sixth solvent to provide an eighth reaction mixture; cooling the eighth reaction mixture and admixing the eighth reaction mixture with methyl trifluoromethansulfonate to form a ninth reaction mixture; warming the ninth reaction mixture, and admixing a substituted alkyne with the ninth reaction mixture to form the tetraanionic pincer ligand supported metallacycloalkylene complex (1).

专利号:US-9267213-B1
优先权日:2005-03-25
标题:Electrochemical deblocking solution for electrochemical oligomer synthesis on an electrode array
发明人:MAURER KARL; COOPER JOHN J
权利人:CUSTOMARRAY INC
摘要:There is disclosed an electrochemical deblocking solution for use on an electrode microarray. There is further disclosed a method for electrochemical synthesis on an electrode array using the electrochemical deblocking solution. The solution and method are for removing acid-labile protecting groups for synthesis of oligonucleotides, peptides, small molecules, or polymers on a microarray of electrodes while substantially improving isolation of deblocking to active electrodes. The method comprises applying a voltage or a current to at least one electrode of an array of electrodes. The array of electrodes is covered by the electrochemical deblocking solution.

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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:Ni-Catalyzed Alkenylation Of Triazolopyridines: Synthesis Of 2,6-Disubstituted Pyridines
作者:Sheng Liu,James Sawicki,Tom G. Driver |发布日期:2012.7.20
摘要:A Synthetic Strategy To Access 2,6-Disubstituted Pyridines From Triazolopyridines Through A Regioselective Nickel-Catalyzed Alkenylation Reaction Of The C7-H Bond Is Described. The N2 Fragment Embedded In The Resulting C-H Functionalized Triazolopyridine Can Be Readily Excised Using Acidic Or Oxidative Conditions To Unmask The Pyridine.

合成参考文献


摘要:Stolley, R. M.; Louie, J., Science of Synthesis Knowledge Updates, (2013) 2, 39.
摘要:Silva, V. L. M.; Pinto, D. C. G. A.; Santos, C. M. M.; Rocha, D. H. A., Science of Synthesis Knowledge Updates, (2022) 3, 349.
摘要:Bredenkamp, A.; Kirsch, S. F., Science of Synthesis Knowledge Updates, (2014) 4, 454.
摘要:Huy, P.; Czekelius, C., Science of Synthesis Knowledge Updates, (2019) 2, 97.
摘要:Tong, M. L.; Kunz, K.; Jaschinski, M.; Holzschneider, K.; Celik, I. E.; Kirsch, S. F., Science of Synthesis Knowledge Updates, (2020) 2, 268.
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