CAS: 915922-38-2; (3-Chloro-4-Ethoxyphenyl)Methanol

该化合物是一种氯化芳香醇,其分子式为C9H11ClO2.该化合物的特征是附在以氯和苯氧功能组取代的苯环上的氢甲基组,使其在有机合成中成为多用途中间体.其结构特性使得能够应用于制药,农用化学品和精细的化学制造.电子提取剂(氯)和电施用(乙氧)替代成分的存在,增强了其在电子生殖和核循环转化中的再活性.该化合物一般在室温下为固体,应储存在惰性条件下,以确保稳定性.其纯度和定义明确的结构使其适合于精确的合成应用,特别是在生物活性分子的开发中.

结构式图片

上下游产品

3-chloro-4-methoxy-benzaldehyde methylmagnesium chloride 4-ethoxy-3-chloro-benzaldehyde

合成工艺路线路线简述

    📜3-氯-4-乙氧基苯甲醛 以100%的收率获得产物(3-氯-4-乙氧基苯)甲醇
    参考文献: Inhibitors Of Acetyl-Coa Carboxylase[fr] Inhibiteurs De L'Acétyl-Coa Carboxylase
    标题: Inhibitors Of Acetyl-Coa Carboxylase[fr] Inhibiteurs De L'Acétyl-Coa Carboxylase
    摘要:本发明涉及作为乙酰辅酶a羧化酶(acc)抑制剂的化合物.该发明还涉及制备这些化合物的方法,含有这些化合物的组合物,以及使用这些化合物进行治疗的方法.

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    专利信息


    专利号:US-4477660-A
    优先权日:1982-11-16
    标 题 :7-(S)-Acylaminocephalosporin sulfones and process
    发明人:HALL DAVID A
    权利人:LILLY CO ELI
    摘要:This invention encompasses 7-(S)-acylamino-3-acetoxymethyl-3-cephem-4-carboxylic acid sulfones and the epimerization process for making them. The epimerization process employs an organic nitrogen base reagent having a pKa between about 9.0 to about 11.5. The compounds of this invention are intermediates in the synthesis of 1-oxa-β-lactam antibiotics.

    专利号:US-4459405-A
    优先权日:1982-11-16
    标 题 :Desacetylcephalosporin sulfones
    发明人:HALL DAVID A
    权利人:LILLY CO ELI
    摘要:7-(S)-Acylamino-3-hydroxymethyl-3-cephem sulfones are disclosed. These compounds are intermediates in the synthesis of 1-oxa β-lactam antibiotics.

    专利号:US-4474879-A
    优先权日:1982-11-16
    标 题 :Process for 3-hydroxymethyl cephalosporin sulfones
    发明人:HEINEY RICHARD E
    权利人:LILLY CO ELI
    摘要:This invention relates to a process for preparing 7-(S)-acylamino-3-hydroxymethyl-3-cephem-4-carboxylic acid sulfones and the salts and esters thereof. The instant process involves contacting a 7-(S)-acylamino-3-acetoxymethyl cephalosporin sulfone in an aqueous solution buffered from about pH 6 to about pH 8 with citrus acetylesterase, which is immobilized on silica gel. The 3-hydroxymethyl cephalosporin sulfones produced by the process of this invention are intermediates in the synthesis of 1-oxa β-lactam antibiotics.

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