CAS: 26893-73-2; 6-Methoxypicolinic Acid

该化合物是一种该化合物是一种甲基氧代代皮酸结构,其主要优势包括它作为有机合成的宝贵中间体的作用,特别是在制药,农用化学和化学协调应用的准备方面. 甲氧基组增强了其在金属催化反应中的回活动性和选择性,使其对电离和设计和催化系统有用. 其定义明确的晶体形式确保了一致性,有利于精确的实验再生. 此外,它在普通有机溶剂中的溶解性简化了合成工作流程的处理. 该化合物在标准条件下的稳定性进一步证明了其在需要可靠性能的研究和工业应用中的实用性.

英文名称6-Methoxypicolinic Acid
中文名称6-甲氧基吡啶-2-羧酸
IUPAC名称6-methoxypicolinic acid
其它别名6-甲氧基皮考啉酸; 6-Methoxy-2-Pyridinecarboxylic Acid; 6-Methoxypicolinic Acid; Methyl 6-Methoxypyridine-2-Carboxylate
CAS编号26893-73-2
MFCD编号:MFCD06800962
EINECS号:626-873-3
分子式:C7H7NO3
分子量:153.14
产品CID: 1248414
产品分类有机原料→分子砌块→芳杂环类化合物→吡啶类化合物

相似结构搜索
InChIKey: KSWBODXXZITTPO-UHFFFAOYSA-N
InChI=1S/C7H7NO3/c1-11-6-4-2-3-5(8-6)7(9)10/h2-4H,1H3,(H,9,10)…
计算化学: 氢键受体数3.0氢键供体数1.0可旋转键数2.0

相似化合物

54221-96-4 26256-72-4 83621-01-6

MSDS等安全信息

GHS象形图
GHS符号GHS07;
注释: Exclamation mark
危险类别特定目标器官毒性 - 单次接触类别3
皮肤腐蚀/刺激类别2
严重眼刺激类别2
严重眼刺激类别2A
警示词Warning(警告)
危险描述H335 |可能引起呼吸道刺激.
H315 |造成皮肤刺激.
H319 |造成严重眼刺激.
防范说明P261-P264-P270-P271-P280-P302+P352-P304+P340-P305+P351+P338-P330-P362+P364-P403+P233-P405-P501
危险等级IRRITANT
危险品标志Xi
安全声明26-36
危险类别码36/37/38
WGK Germany3

欧盟法规

ECHA物质C&L通报

上下游产品

6-Hydroxypicolinic acid methyl iodide 2-(bromomethyl)-6-methoxypyridine (6-methoxy-pyridin-2-yl)-methanol 1,1,1,3,3,3-hexafluoro-2-(4-(2-((6-methoxy-2-pyridinyl)methyl)-4-(2-thiophenylsulfonyl)-1-piperazinyl)phenyl)-2-propanol

合成工艺路线路线简述

6-甲氧基吡啶-2-羧酸甲酯置于sodium Hydroxide体系中,用水用作溶剂,以95%的收率获得6-甲氧基吡啶-2-甲酸
参考文献:Cn114890940
标题:Cn114890940

海关参考信息

2905110000-甲醇
2912110000-甲醛
2915110000-甲酸
2933310010-吡啶
💡 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:US-9676783-B2
优先权日:2008-10-22
标题:Method of treatment using substituted pyrazolo[1,5-A] pyrimidine compounds
发明人：HAAS JULIA; ANDREWS STEVEN W; JIANG YUTONG; ZHANG GAN
权利人:ARRAY BIOPHARMA INC
摘要:Compounds useful in the synthesis of compounds for treating pain, cancer, inflammation, neurodegenerative disease or Typanosoma cruzi infection in a mammal.

专利号:US-11767302-B2
优先权日:2020-10-01
标题 :Reagents and methods for tetrazine synthesis
发明人：FOX JOSEPH M; LAMBERT WILLIAM; FANG YINZHI; AM ENDE CHRISTOPHER WILLIAM; MAHAPATRA SUBHAM; XIE YIXIN; WANG CHUANQI
权利人:UNIV DELAWARE
摘要:Disclosed herein are mono- and di-substituted tetrazines and methods of their preparation and converting an oxetanyl ester to a thio-substituted tetrazine, which is then converted to a mono-substituted tetrazine, a di-substituted tetrazine, or a vinylether disubstituted tetrazine.

专利号:DK-2725028-T3
优先权日:2008-10-22
标题:Substituted pyrazolo [1,5-a] pyrimidine compounds as intermediates in the synthesis of kinase inhibitors TRK

专利号:EP-2725028-A1
优先权日:2008-10-22
标题 :Substituted pyrazolo[1,5-]pyrimidine compounds as intermediates in the synthesis of TRK kinase inhibitors

专利号:EP-2725028-B1
优先权日:2008-10-22
标题 :Substituted pyrazolo[1,5-]pyrimidine compounds as intermediates in the synthesis of TRK kinase inhibitors

专利号:HU-E030413-T2
优先权日:2008-10-22
标题:Substituted pyrazolo[1,5-]pyrimidine compounds as intermediates in the synthesis of TRK kinase inhibitors