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136255

2-甲基-4(5)-硝基咪唑

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

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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
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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

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

Exclamation mark
GHS07

signalword

Warning

hcodes

H302

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
WXBD6652V
WXBD5026V
WXBD4428V
WXBD2268V
WXBD0747V

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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
S Yang
Hua xi yi ke da xue xue bao = Journal of West China University of Medical Sciences = Huaxi yike daxue xuebao, 30(3), 345-346 (2002-09-06)
The 2-methyl-5(4)-nitromidazole(BH) is an ampholyte with acid and base. It is an intermediate of metronidazole. The amphoteric dissociation constant of BH determined by equimolar UV-spectrophotometry. The acidic dissociation constant pKa is 9.64 +/- 0.04 and the basic dissociation constant pKb
Fa-qing Ye et al.
Yao xue xue bao = Acta pharmaceutica Sinica, 40(2), 132-135 (2005-05-07)
To study the synthesis and antibacterial activity of ciprofloxacin derivatives. Ciprofloxacin derivatives were synthesized primarily from 2-methyl-5-nitroimidazol and ciprofloxacin through nucleophilic substitution. The antibacterial activity of the synthesized compounds were tested. Nine new compounds were synthesized. The structure of the
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货号GTIN
136255-50G04061838731258
136255-250G04061838731241