CAS: 24157-81-1; 2,6-Diisopropylnaphthalene

该化合物是一种高纯度有机化合物,其特点是在2和6个位置以异丙基组替代异丙基团,这种结构具有极佳的热稳定性和化学抗药性,适合在恶劣条件下需要强力性能的应用,其低挥发性和高沸点增强了其作为溶剂或高温工艺中间体的效用.此外,2,6-DIPN表现出与聚合物和树脂的兼容性,有助于其在特殊材料配方中的使用.该化合物的发育障碍也有利于合成化学的选择性反应,在精密制造和催化方面提供了优势.

结构式图片

相似化合物

3905-64-4 6158-45-8 939-27-5

欧盟法规

REACH注册ECHA物质ECHA物质C&L通报REACH预注册

上下游产品

CAS号91-20-3 萘 | CAS号187737-37-7 propene | CAS号67-63-0 异丙醇 | CAS号2027-17-0 2-异丙基萘 | CAS号51113-41-8 1,6-bis(isoprop... | CAS号75-26-3 2-溴丙烷 | CAS号6158-45-8 1-异丙基萘 | CAS号105443-43-4 2-(2-hydroperox... | CAS号107208-69-5 6-乙酰基-2-异丙基萘 | CAS号52387-51-6 2,6-diacetylnap... | CAS号1141-38-4 2,6-萘二羧酸 | CAS号33627-01-9 6-acetyl-2-naph... | CAS号103091-56-1 6-propan-2-ylna... | CAS号2027-17-0 2-异丙基萘 | CAS号6158-45-8 1-异丙基萘 | CAS号40458-98-8 2,7-二异丙基萘

合成工艺路线路线简述

    Silver Trifluoromethanesulfonate 反应生成2,6-二异丙基萘
    参考文献:Nagao,Yukio;Yamada,Tehruaki
    标题:Nagao,Yukio;Yamada,Tehruaki

    海关参考信息

    专利信息


    专利号:US-8637690-B2
    优先权日:2008-02-27
    标题 :Hybrid organic-inorganic material IM-19 and method of preparing same
    发明人:CHAPLAIS GERALD; SIMON-MASSERON ANGELIQUE; PATARIN JOEL; BATS NICOLAS; BAZER-BACHI DELPHINE
    权利人:CHAPLAIS GERALD; SIMON-MASSERON ANGELIQUE; PATARIN JOEL; BATS NICOLAS; BAZER-BACHI DELPHINE; IFP Energies Nouvelles
    摘要:The invention relates to a novel hybrid organic-inorganic material containing an inorganic network of metal centers based on the element gallium, connected to each other by organic bridges, to the preparation and to the use thereof. The invention also relates to an intermediate solid obtained during the synthesis of said hybrid organic-inorganic material.

    专利号:US-5286902-A
    优先权日:1991-04-15
    标题:Process for preparation of 2-(6-methoxy-2-naphthyl)propionic acid and intermediates therefor utilizing 2,6-diisopropylnaphthalene
    发明人:JAMES DUSTIN K; KOMIN ANDREW P; SIEGMAN JOHN R
    权利人:KOCH IND INC
    摘要:A process is disclosed for the synthesis of 2-(6-methoxy-2-naphthyl)propionic acid that utilizes 2,6-diisopropylnaphthalene.

    专利号:US-11919928-B2
    优先权日:2016-03-16
    标题 :Method for producing dihydrotentoxin
    发明人:KUBO TAKASHI; MACHIDA MASAYUKI; FUJIOKA TOMONORI; YAMAGUCHI Shigenari; KAWAI KIYOSHI
    权利人:KUMIAI CHEMICAL INDUSTRY CO
    摘要:An object of the present invention is to identify an enzyme having activity of synthesizing dihydrotentoxin that is a tentoxin precursor and an enzyme having activity of synthesizing tentoxin using dihydrotentoxin as a substrate. The present invention concerns a tentoxin synthesis-related gene encoding a protein comprising the amino acid sequence of SEQ ID NO: 16 and having activity of nonribosomal peptide synthesis of dihydrotentoxin and a tentoxin synthesis-related gene encoding a protein comprising the amino acid sequence of SEQ ID NO: 18 and having activity of converting dihydrotentoxin to tentoxin.

    专利号:US-5268523-A
    优先权日:1989-07-24
    标 题 :Selective sorption of dialkylated multinuclear aromatic compounds
    发明人:FELLMANN JERE D; WENTRCEK PAUL R; KILNER PETER H
    权利人:CATALYTICA INC
    摘要:PCT No. PCT/US90/04153 Sec. 371 Date Jan. 23, 1992 Sec. 102(e) Date Jan. 23, 1992 PCT Filed Jul. 24, 1990.The invention relates to a process for the separation cf various dialkyl multinuclear aromatic compounds from a feed stream of mixed isomers of those compounds. A shape selective adsorbent is employed resulting in a process that is more efficient than processes based upon prior separation techniques. Of special interest are combination processes involving synthesis steps followed by sorption steps using the same shape selective materials.

    专利号:RU-2186767-C2
    优先权日:1997-07-09
    标 题 :Method of synthesis of hydroperoxides

    专利号:CN-101530810-B
    优先权日:2009-04-09
    标题:Supported Molecular Sieve Catalyst and Its Application in the Synthesis of 2,6-Naphthalene Dicarboxylic Acid
    武汉弘德悦欣医药科技有限公司
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    信用代码: 91420102MA4K4WB79G法定代表人:袁洪杰
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    成立日期:2019-07-31登记机关:武汉市江岸区市场监督管理局
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    2,6-二异丙基萘
    2,6-Diisopropylnaphthalene
    产品图片纯度:98
    250kg/drum
    第 1 / 1 页

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    ✅ COA系统入驻 | 共享模式

    合成参考文献


    摘要:S120 | DUSTCT2024 | Substances from Second NORMAN Collaborative Dust Trial | DOI:10.5281/zenodo.13835254
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