CAS: 6379-73-3; 4-Isopropyl-2-Methoxy-1-Methylbenzene

该化合物是来自单脂酚的单脂酚的有机化合物,具有芳香特性,通常因其香味而得到承认,这种化合物在室温下无色可粉黄,可溶于有机溶剂;甲丙基乙醚的抗微生物和抗氧化活动,使其对食品保存和可能的治疗应用感兴趣;其分子结构包括一种甲氧基化合物,有助于其回动和与生物系统的互动;此外,由于其芳香特征,经常研究其在调味和香味工业中的潜在用途;安全数据表明,尽管该化合物具有低毒性,但应遵循适当的处理和使用准则,以减少与接触有关的任何风险;

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

methanol carvacrol dimethyl sulfate methyl iodidep-menth-4-en-2-one 2-methoxyterephthalic acid tetrabromo-o-cresol 5-isopropyl-4-iodo-2-methyl-anisole

合成工艺路线路线简述

    📜2-甲基-5-异丙基苯胺置于sodium Hydroxide,硫酸体系中,化学反应生成 香芹酚甲醚
    参考文献:229.芳香族化合物中烷基的体积效应.的第2部分i.影响:对一组6-二硝化cr 1-[r 2 Alk
    标题:229.芳香族化合物中烷基的体积效应.的第2部分i.影响:对一组6-二硝化cr 1-[r 2 Alk
    摘要:
    DOI:10.1039/jr9330000977

    海关参考信息

    专利信息


    专利号:US-7786259-B2
    优先权日:2001-05-23
    标题:Attachment and elaboration strategies for inverse peptide synthesis
    发明人:GUTHEIL WILLIAM G
    权利人:UNIV MISSOURI
    摘要:The present invention provides a process for preparing an immobilized peptide derivative of formula (Vb): n ncomprising reacting a functionalized solid support comprising Sub-L wherein Sub is a solid support and L is a cleavable linker, with H—[NH—A—C(O)]—O(tBu), then reacting the immobilized product with compound of the formula RHN—A—C(O)OH, wherein the RHN—A—C(O) group is the residue of a N-protected α-amino acid, in the presence of a coupling agent, to yield an immobilized peptide derivative of the formula (Vb).

    专利号:US-9890111-B2
    优先权日:2008-07-21
    标题 :Crystal structure of bifunctional transglycosylase PBP1b from E. coli and inhibitors thereof
    发明人:WONG CHI HUEY; MA CHE ALEX; CHENG TING JEN RACHEL; CHENG WEI CHIEH
    权利人:ACADEMIA SINICA
    摘要:The crystal structure at 2.16 â„« resolution of the full-length bacterial bifunctional transglycosylase penicillin-binding protein 1b (PBP1b) from Escherichia coli , in complex with its inhibitor moenomycin, is provided. The atomic coordinates of the complex as well as the moenomycin binding site are provided. Three dimensional structures of amino acid residues involved in moenomycin binding and transglycosylation activity are identified. Binding site for peptidoglycan synthesis inhibitors comprising inhibitor-binding site comprises amino acid residues from at least one of transglycosylase (TG), UvrB domain 2 homolog (UB2H) and transmembrane (TM) domains of PBP1b are identified at an atomic level of resolution. Methods for rational drug design based on the atomic coordinates are provided. Methods for screening for antibiotics based on anisotropic binding assay and transglycosylase inhibitor assays are provided. Novel antibiotics based on the screening assays of the invention are disclosed.

    专利号:CN-109810062-B
    优先权日:2019-01-24
    标题:Phenylimidazole derivative, synthesis method thereof and application of phenylimidazole derivative in pesticide

    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]: Dorman Hj, Et, Al. Antimicrobial Agents From Plants: Antibacterial Activity Of Plant Volatile Oils. J Appl Microbiol. 2000 Feb;88(2):308-16.
    [参考文献]: Ultee A, Et, Al. The Phenolic Hydroxyl Group Of Carvacrol Is Essential For Action Against The Food-Borne Pathogen Bacillus Cereus. Appl Environ Microbiol. 2002 Apr;68(4):1561-8.

    合成参考文献


    摘要:Fogel, M. S.; Shellnutt, Z. S.; Koide, K., Science of Synthesis: Dearomatizations, (2026) .
    📝 需求与反馈
    尽可能描述清楚需求与问题信息
    ×

    通知