跳转至内容
Merck
所有图片(1)

Key Documents

View All Documentation

196940

Sigma-Aldrich

1-(2-氨基苯基)吡咯

≥98%

登录查看公司和协议定价
所有图片(1)

About This Item

经验公式（希尔记法）:
C10H10N2
CAS号:
6025-60-1
分子量:
158.20
EC號碼:
227-884-2
MDL號碼:
MFCD00005344
分類程式碼代碼:
12352100
PubChem物質ID:
24851811
NACRES:
NA.22

化驗

≥98%

形狀

solid

mp

96-98 °C (lit.)

SMILES 字串

Nc1ccccc1-n2cccc2

InChI

1S/C10H10N2/c11-9-5-1-2-6-10(9)12-7-3-4-8-12/h1-8H,11H2

InChI 密鑰

GDMZHPUPLWQIBD-UHFFFAOYSA-N

相关类别

一般說明

1-(2-Aminophenyl)pyrrole participates in Pt(IV)-catalyzed hydroamination triggered cyclization reaction to yield fused pyrrolo [1,2-a] quinoxalines. It reacts with aromatic or heteroaromatic aldehydes in ethanol and catalytic amounts of acetic acid to yield 4,5-dihydropyrrolo[1,2-a]quinoxalines. Thin films of poly(1-(2-aminophenyl)pyrrole) has been prepared via oxidative electropolymerization.

應用

1-(2-Aminophenyl)pyrrole was used in the synthesis of 4-substituted pyrrolo[1,2-a]quinoxaline derivatives.

象形圖

Exclamation mark
GHS07

訊號詞

Warning

危險分類

Acute Tox. 4 Oral - Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

標靶器官

Respiratory system

儲存類別代碼

11 - Combustible Solids

水污染物質分類（WGK）

WGK 3

閃點（°F）

Not applicable

閃點（°C）

Not applicable

個人防護裝備

dust mask type N95 (US), Eyeshields, Gloves

从最新的版本中选择一种：

分析证书(COA)

Lot/Batch Number
MKCQ6285
MKCP0401
MKCN3984
MKBX6701V
MKBV9455V

没有发现合适的版本？

如果您需要特殊版本，可通过批号或批次号查找具体证书。

搜索COA

已有该产品？

在文件库中查找您最近购买产品的文档。

访问文档库

Nitin T Patil et al.
The Journal of organic chemistry, 75(10), 3371-3380 (2010-04-16)
A PtCl(4)-catalyzed hydroamination-triggered cyclization strategy to access biologically interesting N-containing heterocycles such as pyrrolo[1,2-a]quinoxalines, indolo[1,2-a]quinoxalines, and indolo[3,2-c]quinolines is described. The reaction makes use of aminoaromatics such as 1-(2-aminophenyl)pyrroles, N-(2-aminophenyl)indoles, 2-(2-aminophenyl)indoles, and alkynes having a tethered hydroxyl group. Mechanistically, the reaction
Jean Guillon et al.
Bioorganic & medicinal chemistry, 15(1), 194-210 (2006-10-20)
An original series of 4-substituted pyrrolo[1,2-a]quinoxaline derivatives, new structural analogues of Galipea species quinoline alkaloids, was synthesized from various substituted 2-nitroanilines via multistep heterocyclizations and tested for in vitro antiparasitic activity upon Leishmania amazonensis and Leishmania infantum strains. Structure-activity relationships
Photoelectrochemical studies on poly [1-(2-aminophenyl) pyrrole]-Creation of a photoactive inorganic-organic semiconductor interface (IOI).
Kasem KK, et al.
Canadian Journal of Chemistry, 87(8), 1109-1116 (2009)
A Versatile Synthesis of 4, 5-Dihydropyrrolo [1, 2-a] quinoxalines.
Abonia R, et al.
Journal of Heterocyclic Chemistry, 38(3), 671-674 (2001)

我们的科学家团队拥有各种研究领域经验，包括生命科学、材料科学、化学合成、色谱、分析及许多其他领域.

联系技术服务部门