CAS: 696-45-7; 4-Amino-6-Methoxypyrimidine

该化合物是具有其青米丁环结构特征的有机化合物,这是一个六人芳香循环,含有1号阵地和3号阵地的两个氮原子. 该化合物在6号阵地和4号阵地的冰氧(-OCH3)组和氨基(-NH2)组中具有甲氧基(-OCH3),通常是白色至白色的固体,由于存在氨水和酒精等极溶剂,可溶于水和酒精等极地溶剂.该化合物对包括药用化学在内的各个领域具有兴趣,因为它潜在的生物活动,包括抗微生物和抗舌素特性,其反应力可归因于在场的功能组,可以进行各种化学修改.应参考安全数据,以便处理任何化学物质,以确保在使用期间采取适当的预防措施.

英文名称4-Amino-6-Methoxypyrimidine
中文名称4-氨基-6-甲氧基嘧啶
IUPAC名称6-methoxypyrimidin-4-amine
其它别名4-Pyrimidinamine, 6-Methoxy-; 4-Amino-6-Methoxypyrimidine; 6-Methoxy-Pyrimidin-4-Ylamine; 6-Methoxypyrimidin-4-Ylamine
CAS编号696-45-7
MFCD编号:MFCD00129983
EINECS号:626-150-2
分子式:C5H7N3O
分子量:125.13
产品CID: 1692130
产品分类有机原料→分子砌块→芳杂环类化合物→嘧啶类化合物

相似结构搜索
InChIKey: VELRBZDRGTVGGT-UHFFFAOYSA-N
InChI=1S/C5H7N3O/c1-9-5-2-4(6)7-3-8-5/h2-3H,1H3,(H2,6,7,8)…
计算化学: 氢键受体数4.0氢键供体数1.0可旋转键数1.0

相似化合物

1124-73-8 23132-67-4 3270-97-1

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
急性毒性类别4(经皮)
急性毒性类别4(经口)
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.
H312 |皮肤接触有害.
H302 |吞咽有害.
防范说明P261-P264-P271-P280-P302+P352-P304+P340-P362-P405-P501
危险等级IRRITANT
UN编号NONH for all modes of transport
危险品标志Xi,Xn
安全声明26-36-36/37/39
危险类别码36/37/38-21/22-6/37/38
WGK Germany3

欧盟法规

ECHA物质C&L通报

上下游产品

CAS号3289-53-0 6-氨基-4-甲氧基-2-甲基硫脲嘧啶 | CAS号101012-11-7 5-溴-2,6-二氯嘧啶-4-胺

合成工艺路线路线简述

海关参考信息

2905110000-甲醇
2909199090-其他醚及其衍生物
💡 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-9751851-B2
优先权日:2013-09-20
标题:Molecules and compositions that inhibit gram negative bacteria and their uses
发明人：BASSLER BONNIE L; SEMMELHACK MARTIN F; DRESCHER KNUT; SIRYAPORN ALBERT; CONRAD-MILLER LAURA C; O'LOUGHLIN COLLEEN T
权利人:UNIV PRINCETON; BASSLER BONNIE L; SEMMELHACK MARTIN F; DRESCHER KNUT; SIRYAPORN ALBERT; MILLER LAURA C; O'LOUGHLIN COLLEEN T
摘要:Antivirulence strategies to combat Pseudomonas aeruginosa , are described. One strategy encompasses synthesis of a series of compounds that inhibit the production of pyocyanin, a redox-active virulence factor produced by this pathogen. A related strategy encompasses synthesis of compounds that inhibit the two P. aeruginosa quorum-sensing receptors, LasR and RhlR, inhibit production of pyocyanin, and inhibit biofilm formation.

专利号:WO-2024256496-A1
优先权日:2023-06-14
标题 :[1,2,4]-triazolo[4,3-b]pyridazine derivatives useful as a medicament
发明人：ELIE JONATHAN; GEORGE PASCAL; MIEGE FRÃ‰DÃ‰RIC; MEIJER LAURENT
权利人:PERHA PHARMACEUTICALS
摘要:The present invention relates to a compound of formula (I) or any of its pharmaceutically acceptable salt. The present invention further relates to a synthesis process for manufacturing compound of formula (I) or any of its pharmaceutically acceptable salts, comprising at least a step of reacting a compound of formula (II) with an amine of formula (IV) NHR5R6 for example in a molar ratio ranging from 1 to 20 eq, with respect to the compound of formula (II), in an aprotic solvent or without solvent or else in a protic solvent.

专利号:CN-115215806-B
优先权日:2022-08-16
标题:A kind of synthesis method of sulfonamide-6-methoxypyrimidine

专利号:CN-109293582-A
优先权日:2018-10-29
标题:A kind of preparation method of synthesis 4- amino -2,6- dimethoxypyridin