6-甲氧基吡啶-2-硼酸 N-苯基二乙醇胺酯

• 产品号: 649155
• CAS号: 872054-59-6
• 分子式: C16H19BN2O3
• 分子量: 298.14466

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) (Xi)
• 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