CAS: 1878-49-5; 2-(O-Tolyloxy)Acetic Acid
该化合物是一种该化合物是一种苯氧乙酸脊柱,在苯环的正方位上有一个甲基替代物.这种结构配置具有独特的反应性和功能特性,使其作为有机合成的中间体,特别是在农用化学品,药品和特殊化学品的生产方面,具有宝贵的价值.它的箱式酸组可以进一步衍生,而甲基苯氧基会有助于增加亲脂性和消毒效应.该复合体在极地有机溶剂中表现出中等溶性,便于其在各种反应条件下使用.它在标准处理条件下的稳定性和明确界定的化学行为使它成为研究和工业应用的可靠基石.
- 英文名称2-(O-Tolyloxy)Acetic Acid
- 中文名称(2-甲苯氧基)乙酸
- IUPAC名称2-(o-tolyloxy)acetic acid
- 其它别名Aceticacid, (2-methylphenoxy)- (9CI); Acetic acid, (o-tolyloxy)- (6CI,7CI,8CI); (2-Methylphenoxy)acetic acid; (o-Methylphenoxy)acetic acid; 2-(2-Methylphenoxy)acetic acid; 2-(o-Tolyloxy)acetic acid; 2-[(2-Methylphenyl)oxy]acetic acid; o-Cresolglycolic acid; o-Cresoxyacetic acid; o-Cresyloxyacetic acid; o-Tolyloxyacetic acid
- CAS编号1878-49-5
- MFCD编号:MFCD00014354
- EINECS号:217-517-4
- FDA UNII编号:PXO85N85G3
- 分子式:C9H10O3分子量:166.17
- 产品CID: 954268
- 产品分类有机原料→分子砌块→芳环类化合物→苯类化合物
物理性质
MSDS等安全信息
欧盟法规
ECHA物质C&L通报REACH预注册上下游产品
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- 合成目标产物 (2-Methylphenoxy)Acetic Acid 主要起始原料 Ethyl (2-Methylphenoxy)Acetate
- (文献来源)合成步骤主要原料 Ethyl (2-Methylphenoxy)Acetate
📜Methyl 2-Methylphenoxy Acetate置于水,Sodium Hydroxide体系中,化学反应生成2-甲基苯氧基乙酸
参考文献:Aza-Michael Addition Of Acrylonitrile With 2-Aryloxymethylbenzimidazole Derivatives Under Microwave Irradiation
标题:Aza-Michael Addition Of Acrylonitrile With 2-Aryloxymethylbenzimidazole Derivatives Under Microwave Irradiation
摘要:在微波辐照下,在无水碳酸钾存在下,开发了一种简单,快速,高效的方法,用于丙烯腈与 2-芳基氧甲基苯并咪唑衍生物的偶氮-迈克尔加成反应.制备了一系列新型 1-氰乙基-2-芳氧基甲基苯并咪唑衍生物,并通过 1H NMR,13C NMR,Ir 光谱和元素分析进行了表征.
Doi:10.3184/030823410X12798039968476
海关参考信息
- 2902300000-甲苯
2905310000-1,2-乙二醇
2912110000-甲醛
2912120000-乙醛 - 💡 提示：海关信息按照顺序优先匹配，如需确认的海关信息，请参考相关资料。
- 详情请参考：📖 海关编码查询和海关进出口税则
专利信息
专利号:WO-9955664-A1
优先权日:1998-04-24
标 题 :Preparation of carbocyclic compounds
发明人：BECKER MARK W; CHAPMAN HARLAN H; KELLY DAPHNE E; KENT KENNETH M; LEW WILLARD; LOUIE MICHAEL S; MCGEE LAWRENCE R; PRISBE ERNEST J; POSTICH MICHAEL J; ROHLOFF JOHN C; SCHULTZE LISA M; YU RICHARD H; ZHANG LIJUN
权利人:GILEAD SCIENCES INC; BECKER MARK W; CHAPMAN HARLAN H; KELLY DAPHNE E; KENT KENNETH M; LEW WILLARD; LOUIE MICHAEL S; MCGEE LAWRENCE R; PRISBE ERNEST J; POSTICH MICHAEL J; ROHLOFF JOHN C; SCHULTZE LISA M; YU RICHARD H; ZHANG LIJUN
摘要:The present invention provides new synthetic methods and compositions. In particular, new methods of preparing intermediates useful in the synthesis of neuraminidase inhibitors and compositions useful as intermediates that are themselves useful in the synthesis of neuraminidase inhibitors are provided.
专利号:US-2020149034-A1
优先权日:2017-03-17
标题:Methods and Compositions for Synthesis of Encoded Libraries
专利号:UA-55431-C2
优先权日:1998-10-06
标题:COMPOUNDS HAVING AUXINAL ACTION AND METHOD OF SYNTHESIS
专利号:CN-117623872-A
优先权日:2023-10-08
标 题 :A kind of synthesis method of 2-methyl-4-chlorine
专利号:TW-568914-B
优先权日:1996-12-23
标题 :Cycloalkyl, lactam, lactone and related compounds, pharmaceutical compositions comprising same, and methods for inhibiting beta-amyloid peptide release and/or its synthesis by use of such compounds
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
合成参考文献
参考文献:10.1093/jxb/ern133
摘要:Christian M, Hannah WB, Lüthen H, Jones AM. Identification of auxins by a chemical genomics approach. J Exp Bot. 2008;59(10):2757–67.
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