(+)-(18-冠-6)-2,3,11,12-四羧酸

• 产品号: 442666
• CAS号: 61696-54-6
• 分子式: C16H24O14
• 分子量: 440.35336
• 纯 度: 97%

产品别名

• 标题: (+)-(18-Crown-6)-2,3,11,12-tetracarboxylic acid
• IUPAC标准名: (2R,3R,11R,12R)-1,4,7,10,13,16-hexaoxacyclooctadecane-2,3,11,12-tetracarboxylic acid
• IUPAC传统名: (2R,3R,11R,12R)-1,4,7,10,13,16-hexaoxacyclooctadecane-2,3,11,12-tetracarboxylic acid
• 别名: (2R,3R,11R,12R)-1,4,7,10,13,16-Hexaoxacyclooctadecane-2,3,11,12-tetracarboxylic acid; (2R,3R,11R,12R)-1,4,7,10,13,16-六氧环十八烷-2,3,11,12-四羧酸

产品登记号

• CAS号: 61696-54-6
• MDL号: MFCD00040514
• Beilstein号: 4240375
• PubChem SID: 24867945

产品性质

• Empirical Formula (Hill Notation): C16H24O14
• 纯度: 97%
• 熔点: 210-212 °C(lit.)
• 比旋光度: [α]20/D +62°, c = 1 in methanol
• 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) (Xi)
• 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: 26-36
• 德国WGK号: 3

产品详细信息

详细说明 (English)

Application
Derived tetracarboxylic acid chloride of this crown ether reacts with meta- and para-xylylene diamines to form chiral captands in high yields.1 Used as a chiral selector in capillary zone electrophoresis for the separation of a variety of optically active amines.2 Synthesis of monoamides.3
Packaging
25, 100 mg in glass bottle

详细说明 (简体中文)

Application
该冠醚的四羧酸氯化物与邻位和对位亚二甲苯基二胺反应生成高产量的手性封端配体。1在毛细管区带电泳中用作手性选择剂，分离不同光学活性的胺。2合成单酰胺类化合物。3
包装
25, 100 mg in glass bottle