物质信息
ID:325095
名称和标识
IUPAC传统名
INDOLE3trifluoroacetyl
IUPAC标准名
2,2,2-trifluoro-1-(1H-indol-3-yl)ethan-1-one
别名
3-(Trifluoroacetyl)indole3-Indolyl trifluoromethyl ketone3-(三氟乙酰基)吲哚
化合物性质
安全信息
危险公开号
36/37/38
GHS危险品标识
急性毒性（口服，皮肤接触，吸入），类别4
皮肤刺激，类别2
眼刺激，类别2
皮肤过敏，类别1
特定目标器官毒性 -一次接触，类别3
GHS警示词
Warning
GHS危险声明
H315-H319-H335
安全公开号
26-36
GHS警示性声明
P261-P305+P351+P338
MSDS下载
欧盟危险性物质标志
刺激性 (Xi)德国WGK号
3
个人保护装置
dust mask type N95 (US), Eyeshields, Gloves
产品相关信息
纯度
99%
Empirical Formula (Hill Notation)
C10H6F3NO
理化性质
熔点
211-214 °C(lit.)
描述信息
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
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
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