物质信息

ID:315279

名称和标识
IUPAC传统名
isoquinolin-4-ylboronic acid
IUPAC标准名
(isoquinolin-4-yl)boronic acid
别名
Isoquinoline-4-boronic acid4-Isoquinolineboronic acid4-异喹啉硼酸Isoquinolin-4-ylboronic acid异喹啉-4-硼酸
数据登录号
化合物性质
安全信息
安全公开号
26
GHS危险品标识
GHS07
急性毒性(口服,皮肤接触,吸入),类别4
皮肤刺激,类别2
眼刺激,类别2
皮肤过敏,类别1
特定目标器官毒性 -一次接触,类别3
GHS警示词
Warning
GHS警示性声明
P261-P305+P351+P338
保存温度
2-8°C
德国WGK号
3
欧盟危险性物质标志
刺激性 刺激性 (Xi)
MSDS下载
个人保护装置
dust mask type N95 (US), Eyeshields, Gloves
GHS危险声明
H315-H319-H335
危险公开号
36/37/38
产品相关信息
Empirical Formula (Hill Notation)
C9H8BNO2
理化性质
熔点
230-234 °C
描述信息
General description
可能含不定量的酸酐
包装
1, 5 g in glass bottle
Application
Reactant for:
• Preparation of selective steroid-11β-hydroxylase (CYP11B1) inhibitors for treatment of cortisol dependent diseases1
• Preparation of tetrabutylammonium trifluoroborates2
• Preparation of heteroaryl substituted tetrahydropyrroloijquinolinone derivatives as aldosterone synthase inhibitors3
• Synthesis of aminoarylpyridazines as selective CB2 agonists for treatment of inflammatory pain4
• Preparation of acyl substituted indoles via palladium-catalyzed domino coupling/carbonylation/Suzuki coupling of dibromoethenylanilines5
• Synthesis of antagonists of bacterial quorum sensing6
• Preparation of potassium heteroaryl trifluoroborates from boronic acids and their use as coupling partners with various aryl and heteroaryl halides in Suzuki-Miyaura cross-coupling reactions7
分子图谱
暂无数据
点击上传数据
参考文献
暂无数据
点击上传数据