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Merck

549177

Sigma-Aldrich

5-氨基-3-(4-甲氧苯基)-1-苯基吡唑

97%

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About This Item

经验公式(希尔记法):
C16H15N3O
CAS号:
分子量:
265.31
MDL编号:
UNSPSC代码:
12352100
PubChem化学物质编号:

方案

97%

表单

solid

mp

192-196 °C (lit.)

SMILES字符串

COc1ccc(cc1)-c2cc(N)n(n2)-c3ccccc3

InChI

1S/C16H15N3O/c1-20-14-9-7-12(8-10-14)15-11-16(17)19(18-15)13-5-3-2-4-6-13/h2-11H,17H2,1H3

InChI key

LMLGFNHDEGGHOJ-UHFFFAOYSA-N

一般描述

5-Amino-3-(4-methoxyphenyl)-1-phenylpyrazole belongs to a family of 5-aminopyrazole derivatives, which are bioactive agents. They find a wide range of applications in the pharmaceutical and agrochemical industries.

应用

5-Amino-3-(4-methoxyphenyl)-1-phenylpyrazole (3-(4-methoxyphenyl)-1-phenyl-1H-pyrazol-5-amine) may be used in the preparation of pyrazolo[3,4-b]pyridines derivatives with potent anti-inflammatory activity against interleukin-6 (IL-6).

象形图

Exclamation mark

警示用语:

Warning

危险声明

危险分类

Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

靶器官

Respiratory system

储存分类代码

11 - Combustible Solids

WGK

WGK 3

闪点(°F)

Not applicable

闪点(°C)

Not applicable

个人防护装备

dust mask type N95 (US), Eyeshields, Gloves


历史批次信息供参考:

分析证书(COA)

Lot/Batch Number

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访问文档库

Approaches towards the synthesis of 5-aminopyrazoles.
Aggarwal R, et al.
Beilstein Journal of Organic Chemistry, 7(1), 179-197 (2011)
Sandip B Bharate et al.
Bioorganic & medicinal chemistry, 16(15), 7167-7176 (2008-07-16)
In the present article, we have synthesized three different series of pyrazolo[3,4-b]pyridines and their structural analogues using novel synthetic strategy involving one-pot condensation of 5,6-dihydro-4H-pyran-3-carbaldehyde/2-formyl-3,4,6-tri-O-methyl-D-glucal/chromone-3-carbaldehyde with heteroaromatic amines. All synthesized compounds were evaluated for their anti-inflammatory activity against TNF-alpha and

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