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1,5,6,7-四氢-4H-吲哚-4-酮_分子结构_CAS_13754-86-4)
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1,5,6,7-四氢-4H-吲哚-4-酮

产品号 357839 公司名称 Sigma Aldrich
CAS号 13754-86-4 公司网站 http://www.sigmaaldrich.com
分子式 C8H9NO 电 话 1-800-521-8956
分子量 135.16316 传 真
纯 度 98% 电子邮件
保 存 Chembase数据库ID: 90694

产品价格信息

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产品别名

标题
1,5,6,7-Tetrahydro-4H-indol-4-one
IUPAC标准名
4,5,6,7-tetrahydro-1H-indol-4-one
IUPAC传统名
1,5,6,7-tetrahydroindol-4-one
别名
4,5,6,7-Tetrahydro-4-oxoindole
NSC 131681

产品登记号

CAS号 13754-86-4
MDL号 MFCD00075438
PubChem SID 24861947

产品性质

Empirical Formula (Hill Notation) C8H9NO
纯度 98%
熔点 188-190 °C(lit.)
GHS危险品标识 GHS07
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) 刺激性(Irritant) (Xi)
MSDS下载 下载链接
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 26-37/39
德国WGK号 3

产品详细信息

详细说明 (English)
Packaging
5 g in glass bottle
Application

• Reactant in synthesis of psammopemmin A as antitumor agent1
• Reactant in synthesis of a 1,3,4,5-tetrahydrobenzindole β-ketoesters and tricyclic tetrahydrobenzindoles via C-H insertion reactions2
• Reactant in preparation of tricyclic indole and dihydroindole derivatives as inhibitors of guanylate cyclase3
• Reactant in preparation of condensed pyrroloindoles via Pd-catalyzed intramolecular C-H bond functionalization of (halobenzyl)pyrroles4
• Reactant in enantioselective preparation of arylalkenyl indoles via asymmetric C-H insertion of rhodium carbenoids followed by Cope rearrangement-elimination5
详细说明 (简体中文)
包装
5 g in glass bottle
Application

• Reactant in synthesis of psammopemmin A as antitumor agent1
• Reactant in synthesis of a 1,3,4,5-tetrahydrobenzindole β-ketoesters and tricyclic tetrahydrobenzindoles via C-H insertion reactions2
• Reactant in preparation of tricyclic indole and dihydroindole derivatives as inhibitors of guanylate cyclase3
• Reactant in preparation of condensed pyrroloindoles via Pd-catalyzed intramolecular C-H bond functionalization of (halobenzyl)pyrroles4
• Reactant in enantioselective preparation of arylalkenyl indoles via asymmetric C-H insertion of rhodium carbenoids followed by Cope rearrangement-elimination5

参考文献