ChemicalBook--->CAS DataBase List--->527-73-1

527-73-1

527-73-1 Structure

527-73-1 Structure
IdentificationMore
[Name]

2-Nitroimidazole
[CAS]

527-73-1
[Synonyms]

2-NITROIMIDAZOLE
AZOMYCIN
AZOMYCINE
11a
2-nitro-1h-imidazol
2-nitro-1h-imidazole
2-nitro-imidazol
amicin
ro05-9129
2-Nitroimidazole,98%
1H-Imidazole, 2-nitro-
2-Nitroimidaxole
2-nitro-imidazo
2-NITROMIDAZOLE
[EINECS(EC#)]

208-425-5
[Molecular Formula]

C3H3N3O2
[MDL Number]

MFCD00005185
[Molecular Weight]

113.07
[MOL File]

527-73-1.mol
Chemical PropertiesBack Directory
[Appearance]

Pale Yellow Solid
[Melting point ]

287 °C (dec.) (lit.)
[Boiling point ]

211.75°C (rough estimate)
[density ]

1.5988 (rough estimate)
[refractive index ]

1.4264 (estimate)
[storage temp. ]

Sealed in dry,Room Temperature
[solubility ]

NH4OH: soluble50mg/mL, clear, yellow to orange
[form ]

Powder
[pka]

8.72±0.10(Predicted)
[color ]

Light yellow to khaki-green
[Water Solubility ]

insoluble
[Usage]

Antibiotic substance produced by an unidentified Streptomyces
[Detection Methods]

HOLC
[Merck ]

14,921
[BRN ]

116444
[InChIKey]

YZEUHQHUFTYLPH-UHFFFAOYSA-N
[CAS DataBase Reference]

527-73-1(CAS DataBase Reference)
[EPA Substance Registry System]

527-73-1(EPA Substance)
Safety DataBack Directory
[Symbol(GHS) ]

Exclamation Mark (GHS07)
GHS07
[Signal word ]

Warning
[Hazard statements ]

H302
[Precautionary statements ]

P301+P312+P330
[Hazard Codes ]

Xn,T
[Risk Statements ]

R22:Harmful if swallowed.
R36/37/38:Irritating to eyes, respiratory system and skin .
R23/24/25:Toxic by inhalation, in contact with skin and if swallowed .
[Safety Statements ]

S26:In case of contact with eyes, rinse immediately with plenty of water and seek medical advice .
S36:Wear suitable protective clothing .
S45:In case of accident or if you feel unwell, seek medical advice immediately (show label where possible) .
S36/37/39:Wear suitable protective clothing, gloves and eye/face protection .
[RIDADR ]

UN 2811 6.1/PG 3
[WGK Germany ]

3
[RTECS ]

NI7875000
[TSCA ]

Yes
[HazardClass ]

6.1
[PackingGroup ]

III
[HS Code ]

29332990
[Toxicity]

LD50 i.v. in mice: 80 mg/kg (Maeda)
Raw materials And Preparation ProductsBack Directory
[Raw materials]

Ethanol-->Ethyl acetate-->Diethyl ether-->Petroleum ether-->Nitric acid-->Sodium nitrite-->Sodium sulfate-->Fluoroboric acid-->Copper(II) sulfate pentahydrate-->2,2-Diethoxyethylamine-->2-Aminoimidazole hemisulfate-->2-Aminoimidazole
[Preparation Products]

2-Aminoimidazole-->2-nitro-1-(prop-2-ynyl)-1H-imidazole-->N,N-DiMethyl-2-nitro-1H-iMidazole-1-sulfonaMide
Material Safety Data Sheet(MSDS)Back Directory
[msds information]

Azomycin(527-73-1).msds
Hazard InformationBack Directory
[Chemical Properties]

Pale Yellow Solid
[Uses]

2-Nitroimidazole is a antibiotic substance produced by an unidentified Streptomyces,it is used to prepare nitroimidazole substituted boronic acids as precursors for imaging hypoxic tissue 1.It is also used to prepare potential site-selective radiosensitizers for estrogen receptor-rich tumors.
[Uses]

Antibiotic substance produced by an unidentified Streptomyces
[Definition]

ChEBI: An imidazole that is 1H-imidazole substituted at position 2 by a nitro group.
[General Description]

2-Nitroimidazole is a natural antibiotic.
[Synthesis]

imidazol-2-ylamine sulphate

42383-61-9

2-Nitroimidazole

527-73-1

General procedure for the synthesis of 2-nitroimidazole from 2-aminoimidazole sulfate: 2-aminoimidazole sulfate (1.57 g, 6.01 mmol) was dissolved in water (10 mL) and 50% w/v fluoroboric acid (7 mL). The reaction solution was cooled to -20 °C in an acetone/dry ice bath and a solution of sodium nitrite (4.14 g, 59.6 mmol) in water (10 mL) was added slowly and dropwise. The reaction temperature was maintained at -10 °C and stirred for 30 min. Subsequently, the reaction solution was poured into a solution of copper sulfate (20.0 g, 119 mmol) in water (200 mL). Sodium nitrite (4.14 g, 59.6 mmol) was then added and the reaction mixture was stirred for 2 hours at room temperature. After completion of the reaction, the extract was carried out for 6 hours using a continuous extractor with ethyl acetate (200 mL) as the extractant. The organic phases were combined, concentrated under reduced pressure and the residue was recrystallized from ethanol to give the target compound 2-nitroimidazole as yellow needle-like crystals (870 mg, 65% yield).

[storage]

Store at -20°C
[References]

[1] Bioorganic and Medicinal Chemistry Letters, 2011, vol. 21, # 17, p. 5102 - 5106
Spectrum DetailBack Directory
[Spectrum Detail]

2-Nitroimidazole(527-73-1)MS
2-Nitroimidazole(527-73-1)1HNMR
2-Nitroimidazole(527-73-1)13CNMR
2-Nitroimidazole(527-73-1)IR1
2-Nitroimidazole(527-73-1)IR2
2-Nitroimidazole(527-73-1)Raman
Well-known Reagent Company Product InformationBack Directory
[Acros Organics]

2-Nitroimidazole, 98%(527-73-1)
[Alfa Aesar]

2-Nitroimidazole, 98%(527-73-1)
[Sigma Aldrich]

527-73-1(sigmaaldrich)
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