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5-硝基吲哚-2-酮_分子结构_CAS_20870-79-5)
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5-硝基吲哚-2-酮

产品号 653683 公司名称 Sigma Aldrich
CAS号 20870-79-5 公司网站 http://www.sigmaaldrich.com
分子式 C8H6N2O3 电 话 1-800-521-8956
分子量 178.14484 传 真
纯 度 97% 电子邮件
保 存 Chembase数据库ID: 74807

产品价格信息

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产品别名

标题
5-Nitro-2-oxindole
IUPAC标准名
5-nitro-2,3-dihydro-1H-indol-2-one
IUPAC传统名
5-nitro-1,3-dihydroindol-2-one
别名
5-Nitro-1,3-dihydroindole-2-one
NSC 25199
NSC 99066
5-硝基-1,3-二氢-2H-吲哚-2-酮

产品登记号

MDL号 MFCD00456999
CAS号 20870-79-5
PubChem SID 24883978

产品性质

Empirical Formula (Hill Notation) C8H6N2O3
纯度 97%
熔点 233-236 °C
GHS危险品标识 GHS07
GHS警示词 Warning
GHS危险声明 H315-H317-H319-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, Faceshields, Gloves
GHS警示性声明 P261-P280-P305 + P351 + P338
危险公开号 36/37/38-43
安全公开号 26-36/37
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 synthesis of 3-[4-(amino/methylsulfonyl)phenyl]methylene-indolin-2-one derivatives as novel COX-1/2 and 5-LOX inhibitors1
• Reactant for preparation of Aurora kinase inhibitors2
• Reactant for synthesis of 3-substituted 2-indolinone RET inhibitors3
• Reactant for synthesis of 4-azachromeno[2,3-b]indol-11(6H)-ones and derivatives as analogs of ellipticine4
• Reactant for preparation of [18F]fluorobenzylidene-indolinone as possible tyrosine kinase inhibitor for PET tumor imaging5
• Reactant for preparation of 3-substituted indolin-2-ones as neuroprotective and toxic agents6
详细说明 (简体中文)
包装
1, 5 g in glass bottle
Application

• Reactant for synthesis of 3-[4-(amino/methylsulfonyl)phenyl]methylene-indolin-2-one derivatives as novel COX-1/2 and 5-LOX inhibitors1
• Reactant for preparation of Aurora kinase inhibitors2
• Reactant for synthesis of 3-substituted 2-indolinone RET inhibitors3
• Reactant for synthesis of 4-azachromeno[2,3-b]indol-11(6H)-ones and derivatives as analogs of ellipticine4
• Reactant for preparation of [18F]fluorobenzylidene-indolinone as possible tyrosine kinase inhibitor for PET tumor imaging5
• Reactant for preparation of 3-substituted indolin-2-ones as neuroprotective and toxic agents6

参考文献