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Merck
CN

195650

2-硝基咪唑

98%

别名:

吖素

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关于此项目

经验公式(希尔记法):
C3H3N3O2
化学文摘社编号:
分子量:
113.07
UNSPSC Code:
12352005
NACRES:
NA.22
PubChem Substance ID:
EC Number:
208-425-5
Beilstein/REAXYS Number:
116444
MDL number:
Assay:
98%
Form:
solid
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InChI key

YZEUHQHUFTYLPH-UHFFFAOYSA-N

InChI

1S/C3H3N3O2/c7-6(8)3-4-1-2-5-3/h1-2H,(H,4,5)

SMILES string

[O-][N+](=O)c1ncc[nH]1

assay

98%

form

solid

mp

287 °C (dec.) (lit.)

functional group

nitro

Quality Level

General description

2-硝基咪唑是一种天然抗生素

Application

2-硝基咪唑用于合成:
  • 2-(2-硝基-1H-咪唑-1-基)乙基氨基甲酸叔丁酯
  • 1-(2-(丁基二甲硅烷氧基)乙基)-2-硝基-1H-咪唑
  • 2-氟-N-(2-(2-硝基-1H-咪唑-1-基)乙基)乙酰胺
  • 2-(2-甲基-5-硝基-1H-咪唑-1H-基)乙基-2-氟乙酸酯
  • 放射性标记前体 - 溴取代的类似物
  • 硝基咪唑取代的硼酸,缺氧组织成像的前体
  • 富含雌激素受体的肿瘤的潜在位点选择性放射增敏剂

Packaging

无底玻璃瓶。内含物装在插入的融合锥内。

Analysis Note

溶解度:
50 mg/mL,NH4OH:可溶、澄清、黄绿色至深黄绿色至深黄色

signalword

Warning

hcodes

pictograms

Exclamation mark

Hazard Classifications

Acute Tox. 4 Oral

存储类别

6.1C - Combustible acute toxic Cat.3 / toxic compounds or compounds which causing chronic effects

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

dust mask type N95 (US), Eyeshields, Faceshields, Gloves


历史批次信息供参考:

分析证书(COA)

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Environmental microbiology, 13(4), 1010-1017 (2011-01-20)
Antibiotic resistance in pathogens can be mediated by catabolic enzymes thought to originate from soil bacteria, but the physiological functions and evolutionary origins of the enzymes in natural ecosystems are poorly understood. 2-Nitroimidazole (2NI) is a natural antibiotic and an
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