N9009
5-硝基-2-糠醛半卡巴腙
别名:
5-硝基-2-呋喃甲醛半卡腙, NFZ, 呋喃西林, 硝呋醛
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关于此项目
经验公式（希尔记法）:
C6H6N4O4
化学文摘社编号:
分子量:
198.14
EC Number:
200-443-1
UNSPSC Code:
12352100
MDL number:
Beilstein/REAXYS Number:
86403
InChI key
IAIWVQXQOWNYOU-FPYGCLRLSA-N
InChI
1S/C6H6N4O4/c7-6(11)9-8-3-4-1-2-5(14-4)10(12)13/h1-3H,(H3,7,9,11)/b8-3+
SMILES string
NC(=O)N\N=C\c1ccc(o1)[N+]([O-])=O
mp
242-244 °C (lit.)
storage temp.
2-8°C
signalword
Warning
Hazard Classifications
Acute Tox. 4 Oral - Aquatic Chronic 3 - Carc. 2 - Muta. 2 - Repr. 2 - Skin Sens. 1 - STOT RE 2
target_organs
male reproductive organs
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, Faceshields, Gloves
法规信息
新产品
此项目有
Rasha A Shaalan et al.
Journal of chromatographic science, 48(8), 647-653 (2010-09-08)
In this work, a simple, rapid, and selective high-performance liquid chromatography (HPLC) method with diode array detection was developed for the simultaneous determination of nitrofurazone (NZ) and lidocaine hydrochloride (LD). The chromatographic separation was achieved by using Zorbax Eclipse XDB-C(18)
R Pickard et al.
Health technology assessment (Winchester, England), 16(47), 1-197 (2012-12-04)
Catheter-associated urinary tract infection (CAUTI) is a major preventable cause of harm for patients in hospital and incurs significant costs for health-care providers such as the UK NHS. Many preventative strategies and measures have been introduced to minimise CAUTI risk
Robert Pickard et al.
Lancet (London, England), 380(9857), 1927-1935 (2012-11-09)
Catheter-associated urinary tract infection (CAUTI) is a major preventable cause of harm for patients in hospital. We aimed to establish whether short-term routine use of antimicrobial catheters reduced risk of CAUTI compared with standard polytetrafluoroethylene (PTFE) catheterisation. In our parallel
Ali Ryan et al.
Scientific reports, 1, 63-63 (2012-02-23)
Azoreductases are well known for azo pro-drug activation by gut flora. We show that azoreductases have a wider role in drug metabolism than previously thought as they can also reduce and hence activate nitrofurazone. Nitrofurazone, a nitroaromatic drug, is a
Yongnian Ni et al.
Biosensors & bioelectronics, 38(1), 245-251 (2012-06-22)
Electrochemical behavior of nitrofurazone (NFZ) was investigated with the use of cyclic voltammetry (CV) and differential pulse voltammetry (DPV) methods. The pH-dependence of NFZ was studied at a glassy carbon electrode (GCE) in ethanol/Britton-Robinson buffer (30:70), and short-lived nitro-radicals were
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