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152684-30-5

5-bromo-2-methoxy-3-nitro-pyridine

CAS: 152684-30-5;58819-77-5

Molecular Formula: C6H5BrN2O3

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152684-30-5 - Names and Identifiers

Name 5-bromo-2-methoxy-3-nitro-pyridine
Synonyms 2-Methoxy-3-Nitro-5-Bromopyridine
2-METHOXY-3-NITRO-5-BROMOPYRIDINE
5-Bromo-2-methoxy-3-nitropyridine
5-BROMO-2-METHOXY-3-NITRO-PYRIDINE
5-bromo-2-methoxy-3-nitro-pyridine
Pyridine,5-bromo-2-methoxy-3-nitro-
pyridine, 5-bromo-2-methoxy-3-nitro-
CAS 152684-30-5
58819-77-5
InChI InChI=1/C6H5BrN2O3/c1-12-6-5(9(10)11)2-4(7)3-8-6/h2-3H,1H3
InChIKey YRVHFGOAEVWBNS-UHFFFAOYSA-N

152684-30-5 - Physico-chemical Properties

Molecular FormulaC6H5BrN2O3
Molar Mass233.02
Density1.730±0.06 g/cm3(Predicted)
Melting Point88.0 to 92.0 °C
Boling Point282.0±35.0 °C(Predicted)
Flash Point124.339°C
Vapor Presure0.006mmHg at 25°C
pKa-2.99±0.20(Predicted)
Storage ConditionInert atmosphere,Room Temperature
Refractive Index1.587
MDLMFCD07374968

152684-30-5 - Risk and Safety

Hazard SymbolsXi - Irritant
Irritant
Risk Codes36/37/38 - Irritating to eyes, respiratory system and skin.
Safety Description26 - In case of contact with eyes, rinse immediately with plenty of water and seek medical advice.
WGK Germany3
Hazard ClassIRRITANT

152684-30-5 - Reference Information

use 5-bromo -2-methoxy -3-nitropyridine has the characteristics of easy structural modification, making it the most commonly used molecular group for constructing hole transport materials, host materials and luminescent materials. 5-Bromo-2-methoxy-3-nitropyridine not only has a large π-electron conjugation system, strong electron transfer ability and rigid fused ring structure, but also easy to introduce a variety of functions on its pyridine ring. The group, which makes 5-bromo-2-methoxy-3-nitropyridine have a very wide range of applications in OLED devices, there are significant performance characteristics in different functional layers, so the research in related fields is very active and many important research results have been achieved.
Synthesis method Add 25% wt sodium methoxide methanol solution (2.1
L) to the 5-bromo -2-chloro -3-nitropyridine (1.70kg) suspension in methanol (6.6 L), and stir under 0-5°C nitrogen. Stir the reaction mixture at 5-10°C for 2.75 hours, and then add water (8.5
L). The reaction mixture was cooled to 20-25°C. Then the mixture is concentrated under vacuum, the resulting suspension is filtered, washed with water (8.5L, then 2 x 4.25
L), and the solid is dried under vacuum to obtain the title compound 5-bromo-2-methoxy-3-nitropyridine. White solid, yield (1.37kg). 1H nuclear magnetic resonance (400MHz, chloroform-d)δ(ppm)8.46(s,1H),8.40(s,1
H). Figure 5-Bromo-2-methoxy-3-nitropyridine synthesis route
Last Update:2024-04-09 21:00:56
152684-30-5
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Email: product@acmec-e.com
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Multiple Specifications
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152684-30-5
440662-09-9
183438-24-6
环己基溴化镁
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