CAS: 80099-98-5; 6-Chloropicolinoyl Chloride
- 英文名称6-Chloropicolinoyl Chloride
- 中文名称6-氯-2-吡啶羰酰氯
- IUPAC名称6-chloropicolinoyl chloride
- 其它别名2-Chloro-6-pyridinecarbonylchloride; 6-Chloro-2-pyridinecarbonyl chloride; 6-Chloropicolinic acidchloride; 6-Chloropicolinoyl chloride
- CAS编号80099-98-5
- MFCD编号:MFCD00274531
- EINECS号:863-542-4
- 分子式:C6H3Cl2NO分子量:176.0
- 产品CID: 1794964
- 产品分类医药中间体 → 吡啶类化合物
物理性质
MSDS等安全信息
欧盟法规
C&L通报上下游产品
CAS号4684-94-0 6-氯吡啶-2-羧酸 | CAS号19621-92-2 6-羟基-2-吡啶羧酸 | CAS号5140-72-7 2-溴-6-氯吡啶 | CAS号6636-55-1 2-氯吡啶-6-甲酸甲酯 | CAS号1280786-59-5 6-氯吡啶-2-甲酸叔丁酯 | CAS号98142-19-9 6-Chloropyridin...合成工艺路线路线简述
- 19621-92-2 = 80099-98-5
反应条件:1.1 Reagents: Phosphorus Pentachloride Solvents: Phosphorus Oxychloride
标题:Process For The Preparation Of Carboxylic Acid Chlorides Of Aromatic Nitrogen-Containing Heterocycles
参考文献:European Patent Organization]
1929-82-4 = 80099-98-5
反应条件:1.1 Reagents: Sulfuric Acid Solvents: Water; Rt -> 100 °C; 6 H,100 °C; 100 °C -> 60 °C1.2 Reagents: Ammonia Solvents: Water; 60 °C -> Rt2.1 Reagents: Thionyl Chloride Solvents: Toluene; 2 H,Reflux; Reflux -> Rt
标题:Synthesis Of Picolinafen
作者:Li,Aijun; Et Al
参考文献:Nongyao 日期:2012 卷标:51(6) 页码:416-418
📜6-氯吡啶-2-羧酸置于氯化亚砜体系中,化学反应 6.0H,反应生成 6-氯-2-吡啶羰酰氯
参考文献:酰胺在ch活化中的作用:与l型配体的非共价相互作用,用于芳酰胺的偏硼酸化反应
标题:酰胺在ch活化中的作用:与l型配体的非共价相互作用,用于芳酰胺的偏硼酸化反应
摘要:描述了芳族酰胺间选择性硼化的新概念.已经证明,尽管酯产生对硼烷基化,但是酰胺导致间硼烷基化.为了实现较高的间位选择性,使用了l型双功能配体,该配体与中度扭曲的酰胺羰基的氧原子发生o⋅⋅⋅k非共价相互作用.这种相互作用提供了对元ch活化/基化的特殊控制.
DOI:10.1002/anie.201809929
海关参考信息
- 2912110000-甲醛
2933310010-吡啶
2903110000-一氯甲烷及氯乙烷
2939800000-其他生物碱 - 💡 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-6271379-B1
优先权日:2000-03-08
标题:Intermediates useful for the synthesis of huperzine A
发明人：TUECKMANTEL WERNER; KOZIKOWSKI ALAN P
权利人:UNIV GEORGETOWN
摘要:Intermediates useful for the synthesis of huperzine A represented by the structures below, n and methods for their synthesis, wherein: n R 1 is lower alkyl, benzyl, or substituted benzyl; n X is a suitable leaving group; n Y is an electron withdrawing group that can subsequently be converted into an amino group; n one broken line is present as a carbon—carbon bond and the other broken line is absent, where the broken line forms an unconjugated carbon—carbon double bond, which double bond may be endocyclic whereby n is 3 or the double bond may be exocyclic whereby n is 2.
专利号:RU-2098424-C1
优先权日:1991-02-27
标题:Dipeptide derivatives or their pharmaceutically acceptable salts, methods of their synthesis, antihypertensive pharmaceutical composition
专利号:RO-113989-B1
优先权日:1992-10-22
标 题 :PRAZOLYLOXYPICOLINAMIDE DERIVATIVES, THE PROCESS FOR THEIR PREPARATION, SYNTHESIS INTERMEDIATES, ERBICIDES COMPOSITION AND THE METHOD FOR FIGHTING OF NON-ORGANIC PLANTS
