3-(三氟乙酰基)吲哚

• 产品号: 422223
• CAS号: 14618-45-2
• 分子式: C10H6F3NO
• 分子量: 213.1559496
• 纯 度: 99%

产品别名

• 标题: 3-(Trifluoroacetyl)indole
• IUPAC标准名: 2,2,2-trifluoro-1-(1H-indol-3-yl)ethan-1-one
• IUPAC传统名: INDOLE3trifluoroacetyl
• 别名: 3-Indolyl trifluoromethyl ketone

产品登记号

• MDL号: MFCD00182114
• PubChem SID: 24866420
• CAS号: 14618-45-2

产品性质

• Empirical Formula (Hill Notation): C10H6F3NO
• 纯度: 99%
• 熔点: 211-214 °C(lit.)
• 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)

Packaging
1, 5 g in glass bottle
Application

• Reactant for enantioselective synthesis of indoles via palladium-catalyzed kinetic asymmetrical alkylation1
• Reactant for preparation of N-pyridinyl indolecarboxamides via amidation of aminopyridine derivatives. with indolecarboxylic acid2
• Reactant for preparation of mast cell tryptase inhibitors, starting from indoles; using amidation as the key step3
• Reactant for formation of Michael adducts via Baylis-Hillman reaction4
• Reactant for preparation of indolecarboxamides via haloform cleavage of (trifluoroacetyl)indole with lithium dialkylamides5

详细说明 (简体中文)

包装
1, 5 g in glass bottle
Application

• Reactant for enantioselective synthesis of indoles via palladium-catalyzed kinetic asymmetrical alkylation1
• Reactant for preparation of N-pyridinyl indolecarboxamides via amidation of aminopyridine derivatives. with indolecarboxylic acid2
• Reactant for preparation of mast cell tryptase inhibitors, starting from indoles; using amidation as the key step3
• Reactant for formation of Michael adducts via Baylis-Hillman reaction4
• Reactant for preparation of indolecarboxamides via haloform cleavage of (trifluoroacetyl)indole with lithium dialkylamides5