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6-甲氧基吡啶-2-硼酸 N-苯基二乙醇胺酯_分子结构_CAS_872054-59-6)
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6-甲氧基吡啶-2-硼酸 N-苯基二乙醇胺酯

产品号 649155 公司名称 Sigma Aldrich
CAS号 872054-59-6 公司网站 http://www.sigmaaldrich.com
分子式 C16H19BN2O3 电 话 1-800-521-8956
分子量 298.14466 传 真
纯 度 电子邮件
保 存 Chembase数据库ID: 142656

产品价格信息

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产品别名

标题
6-Methoxypyridine-2-boronic acid N-phenyldiethanolamine ester
IUPAC标准名
2-(6-methoxypyridin-2-yl)-6-phenyl-1,3,6,2-dioxazaborocane
IUPAC传统名
2-(6-methoxypyridin-2-yl)-6-phenyl-1,3,6,2-dioxazaborocane
别名
6-Methoxy-2-pyridineboronic acid-N-phenyldiethanolamine ester

产品登记号

PubChem SID 24883634
MDL号 MFCD08276767
CAS号 872054-59-6

产品性质

联合国危险货物等级 4.1
联合国危险货物编号 3175
联合国危险货物包装类别(PG) 2
德国WGK号 3
GHS危险品标识 GHS02
GHS危险品标识 GHS05
GHS危险品标识 GHS07
GHS警示词 Danger
GHS危险声明 H228-H315-H318-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 P210-P261-P280-P305 + P351 + P338
RID/ADR UN 3175 4.1/PG 2
危险公开号 37/38-41-67
安全公开号 26-39
Empirical Formula (Hill Notation) C16H19BN2O3
熔点 210 °C (dec.)(lit.)

产品详细信息

详细说明 (English)
General description
May contain varying amounts of Isopropanol and N-phenyldiethanolamine as stabilizers
Packaging
1, 5 g in glass bottle
Application
Reactant for:
• Preparation of alkylated sulfonamides via alkylation with alcohols catalyzed by Ag/Mo hybrid1
• Preparation of 7-disubstituted oxyindoles as EP3 receptor antagonists2
• Preparation of N-substituted sulfonamides via ferrous chloride-catalyzed N-alkylation with benzylic alcohols3
• Preparation of (alkyl)hydroxybenzimidazoles, via a O- to N-acyl transfer reaction, as intermediates for EP3 receptor antagonists4
• Preparation of N-arylsulfonyl β-[(aryloxy)indolyl]acrylamides as potent and selective EP3 receptor antagonists5
详细说明 (简体中文)
General description
可能含不定量的异丙醇和 N-苯基二乙醇胺作为稳定剂
包装
1, 5 g in glass bottle
Application
Reactant for:
• Preparation of alkylated sulfonamides via alkylation with alcohols catalyzed by Ag/Mo hybrid1
• Preparation of 7-disubstituted oxyindoles as EP3 receptor antagonists2
• Preparation of N-substituted sulfonamides via ferrous chloride-catalyzed N-alkylation with benzylic alcohols3
• Preparation of (alkyl)hydroxybenzimidazoles, via a O- to N-acyl transfer reaction, as intermediates for EP3 receptor antagonists4
• Preparation of N-arylsulfonyl β-[(aryloxy)indolyl]acrylamides as potent and selective EP3 receptor antagonists5

参考文献