主要文件

查看所有文档

136255

2-甲基-4(5)-硝基咪唑

Name: 2-甲基-4(5)-硝基咪唑
Brand: ALDRICH

99%

别名:

2-甲基-4-硝基-1H-咪唑, 2-甲基-4-硝基咪唑, 2-甲基-5-硝基-1H-咪唑, 2-甲基-5-硝基咪唑, 4-硝基-2-甲基咪唑, 甲硝唑

登录查看组织和合同定价。

选择尺寸

变更视图

关于此项目

经验公式（希尔记法）:

C₄H₅N₃O₂

化学文摘社编号:

696-23-1

分子量:

127.10

UNSPSC Code:

12352005

NACRES:

NA.22

PubChem Substance ID:

24848270

EC Number:

211-790-3

Beilstein/REAXYS Number:

4032

MDL number:

MFCD00151322

Assay:

99%

Form:

powder

技术服务

需要帮助？我们经验丰富的科学家团队随时乐意为您服务。

让我们为您提供帮助

属性

Quality Level

200

assay

99%

form

powder

mp

251-255 °C (lit.)

functional group

nitro

SMILES string

Cc1ncc([nH]1)[N+]([O-])=O

InChI

1S/C4H5N3O2/c1-3-5-2-4(6-3)7(8)9/h2H,1H3,(H,5,6)

InChI key

FFYTTYVSDVWNMY-UHFFFAOYSA-N

说明

Application

2-甲基-4(5)-硝基咪唑被用于研究替硝唑的碱性和酸性水解机制。

pictograms

GHS07

signalword

Warning

hcodes

H302

pcodes

P264 - P270 - P301 + P312 - P501

Hazard Classifications

Acute Tox. 4 Oral

存储类别

11 - Combustible Solids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

dust mask type N95 (US), Eyeshields, Gloves

历史批次信息供参考:

分析证书(COA)

Lot/Batch Number

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

On the hydrolytic behavior of tinidazole, metronidazole, and ornidazole.

Jukka-Pekka K Salo et al.

Journal of pharmaceutical sciences, 92(4), 739-746 (2003-03-28)

Using two UV-spectrophotometric methods, the hydrolysis of tinidazole was studied at pH 1.00-8.45 at 80 degrees C. The reaction followed apparent first-order kinetics throughout the studied range. No kinetic salt effect was detected, indicating that at least one of the

Radiosynthesis and evaluation of two novel 123I-labeled 2-methyl-4-nitroimidazole derivatives as potential infection imaging agents.

Daniel D Rossouw et al.

Nuclear medicine and biology, 32(4), 385-394 (2005-05-10)

The inflammation- and infection-seeking properties of (131)I-labeled ornidazole, a 5-nitroimidazole derivative, have recently been reported. Whole-body images in rabbits showed a more rapid uptake in inflamed areas compared to (67)Ga. In the present study, two novel (123)I-labeled 2-methyl-4-nitroimidazole derivatives were

[Synthesis and antibacterial activity of pyridonecarboxylic acid derivatives containing 2-methyl-5-nitroimidazol].

Fa-qing Ye et al.

Yao xue xue bao = Acta pharmaceutica Sinica, 38(4), 260-263 (2003-08-02)

To study the synthesis and antibacterial activity of pyridonecarboxylic acid derivatives containing 2-methyl-5-nitroimidazol. Pyridonecarboxylic acid derivatives containing 2-methyl-5-nitroimidazol were synthesized primarily from 2-methyl-5-nitroimidazol, norfloxacin, ciprofloxacin, enoxacin via nucleophilic substitution and esterification. The antibacterial activity of the nine target compounds were

查看所有相关文献

全球贸易项目编号

货号	GTIN
136255-50G	04061838731258
136255-250G	04061838731241