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4-异喹啉硼酸_分子结构_CAS_192182-56-2)
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4-异喹啉硼酸

产品号 707929 公司名称 Sigma Aldrich
CAS号 192182-56-2 公司网站 http://www.sigmaaldrich.com
分子式 C9H8BNO2 电 话 1-800-521-8956
分子量 172.97632 传 真
纯 度 电子邮件
保 存 Chembase数据库ID: 12414

产品价格信息

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产品别名

标题
4-Isoquinolineboronic acid
IUPAC标准名
(isoquinolin-4-yl)boronic acid
IUPAC传统名
isoquinolin-4-ylboronic acid
别名
异喹啉-4-硼酸
Isoquinolin-4-ylboronic acid
Isoquinoline-4-boronic acid

产品登记号

CAS号 192182-56-2
MDL号 MFCD03412093

产品性质

Empirical Formula (Hill Notation) C9H8BNO2
熔点 230-234 °C
GHS危险品标识 GHS07
GHS警示词 Warning
GHS危险声明 H315-H319-H335
欧盟危险性物质标志 刺激性(Irritant) 刺激性(Irritant) (Xi)
MSDS下载 下载链接
个人保护装置 dust mask type N95 (US), Eyeshields, Gloves
GHS警示性声明 P261-P305 + P351 + P338
危险公开号 36/37/38
安全公开号 26
保存温度 2-8°C
德国WGK号 3

产品详细信息

详细说明 (English)
General description
May contain varying amounts of anhydride
Packaging
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
详细说明 (简体中文)
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

参考文献