CAS: 101-79-1; 4-(4-Chlorophenoxy)Aniline

该化合物是一种氯化芳香衍生物,其特点是存在苯氧联系和厌食功能组,该化合物主要用作有机合成的中间体,特别是在染料,药品和农用化学的制造方面,其结构特征,包括富电子的厌食和氯苯氧组,使其成为进一步功能化的多用途构件.该化合物在标准条件下具有中等稳定性,由于具有作为芳香矿的潜在回活动性,因此一般会谨慎处理.其定义明确的分子结构确保合成应用的一贯性,使其成为研究和工业过程的可靠选择.

结构式图片

相似化合物

1836-74-4 24900-79-6 40859-51-6

欧盟法规

ECHA物质C&L通报REACH预注册

上下游产品

4-(4-chlorophenoxy)nitrobenzene 1-bromo-4-(4-chlorophenoxy)benzene N-acetyl-4-(4-chlorophenoxy)anilino β-D-glucopyranoside 4-chloro-phenol 1-[4-(4-chloro-phenoxy)-phenyl]-biguanide [4-(4-chloro-phenoxy)-phenyl]-guanidine 1-bromo-4-(4-chlorophenoxy)benzene 1-chloro-4-(4-iodophenoxy)benzene

合成工艺路线路线简述

    📜对硝基二苯醚置于盐酸,氯,溶剂黄146,Tin(Ll) Chloride体系中,化学反应生成4'-氯-4-氨基二苯醚
    参考文献:Scarborough,Journal Of The Chemical Society,1929,P. 2367
    标题:Scarborough,Journal Of The Chemical Society,1929,P. 2367

    专利信息


    专利号:US-4136033-A
    优先权日:1969-11-07
    标 题:6-hydroxypyridone-2 compounds having a cationic group in the 3-position
    发明人:STEINEMANN WILLY
    权利人:SANDOZ LTD
    摘要:Compounds of the formula ##STR1## wherein K.sup.⊕ is a cationic group, preferably heterocyclic, n R is hydrogen or an organic radical, preferably alkyl, phenyl or acyl, n R 1 is hydrogen, hydrocarbyl, substituted hydrocarbyl, heterocyclyl, substituted heterocyclyl, amino or substituted amino, and n A.sup.⊖ is an anion, n Are useful as intermediates in the synthesis of azo dyes of the formula ##STR2## wherein D is an aromatic carbocyclic or heterocyclic diazo component radical, and n K.sup.⊕, r, r 1 and A.sup.⊖ are as defined above.

    专利号:US-4999378-A
    优先权日:1987-10-20
    标题:Phenylcarboxylic acid derivatives
    发明人:FUJII SETSURO; KAWAMURA HIROYUKI; WATANABE SHINICHI
    权利人:OTSUKA PHARMA CO LTD
    摘要:Phenylcarboxylic acid derivatives having the formula: ##STR1## wherein R 1 and R 2 are each H, halogen, alkyl, haloalkyl, alkanoyl, cycloalkyl, nitro, amino, --O--D--R 5 (D is alkylene, R 5 is H, amino, morpholino, carboxyl, phthalimido, phenyl, epoxy), substituted or unsubstituted phenoxy, substituted or unsubstituted phenylalkylamino, carboxylalkenyl, or both form alkylenedioxy; R 3 is H, --E--R 6 (E is alkylene, R 6 is H, carboxyl, cyano, OH, phenylalkoxy, or halogen-substituted phenyl, or phenylcarbamoyl), --CO--G--R 7 (G is alkylene, R 7 is H, substituted or unsubstituted phenylcarbamoyl), substituted or unsubstituted benzoyl, alkenyl, carbamoyl, phenyl, or halophenyl; R 4 is H or alkyl; A is alkylene, alkylene condensed with cycloalkyl ring, or alkenylene; B is alkylene or alkenylene; l is 0 or 1. Said compounds have fatty acid synthesis-inhibitory activity, cholesterol synthesis-inhibitory activity and are useful as antilipidemic agent, prophylactic and treating agent of artherosclerosis, prophylactic and treating agent of obesity, antidiabetics.

    专利号:RU-2072987-C1
    优先权日:1991-09-17
    标 题:Derivatives of 3-cycloalkylpropene-2-amide or their additive salts with mineral or organic bases, method of their synthesis and pharmaceutical composition showing antiinflammatory activity

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    合成参考文献

    参考DOI号:10.1039/c7gc00986k
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