113118-81-3
- Product Name：5-Bromo-3-pyridinecarboxaldehyde
- Molecular Formula：C6H4BrNO
- Purity：99%
- Molecular Weight：186.008
Product Details
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- Molecular Formula:C6H4BrNO
- Molecular Weight:186.008
- Appearance/Colour:solid
- Vapor Pressure:0.0209mmHg at 25°C
- Melting Point:98-102 °C
- Refractive Index:1.619
- Boiling Point:251.1 °C at 760 mmHg
- PKA:1.07±0.20(Predicted)
- Flash Point:105.7 °C
- PSA：29.96000
- Density:1.683 g/cm3
- LogP:1.65660
5-Bromo-3-pyridinecarboxaldehyde(Cas 113118-81-3) Usage
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General Description |
5-Bromo-3-pyridinecarboxaldehyde is a white to off-white crystalline powder with a CAS number of 113118-81-3. It has a molecular weight of 186.008 g/mol and a density of 1.683 g/cm3. Other synonyms for 5-Bromo-3-pyridinecarboxaldehyde include: 5-Bromopyridine-3-Carboxaldehyde, 5-BroMo-3-pyridinecarboxaldehyde, 3-Bromo-5-formylpyridine, 5-bromonicotinaldehyde, and 3-bromopyridine-5-carboxaldehyde. |
| Uses | 5-Bromo-3-pyridinecarboxaldehyde is commonly used as an intermediate in the synthesis of various pharmaceuticals, agrochemicals, and fine chemicals. 5-Bromo-3-pyridinecarboxaldehyde is a pale yellow to brown powder that is soluble in organic solvents such as ethanol and acetone. It is known for its strong, pungent odor. The primary application of 5-Bromo-3-pyridinecarboxaldehyde is as a building block in the synthesis of heterocyclic compounds and pharmaceutical intermediates, making it an important reagent in organic chemistry research and manufacturing. 5-Bromo-3-pyridinecarboxaldehyde is intended for professional manufacturing, research laboratories, and industrial or commercial use only. It is harmful if swallowed, causes skin irritation, and may cause an allergic skin reaction. It can also cause serious eye irritation. |
InChI:InChI=1/C6H4BrNO/c7-6-1-5(4-9)2-8-3-6/h1-4H
113118-81-3 Relevant articles
Synthesis of (±) [5-3H] N′-nitrosoanatabine, a tobacco-specific nitrosamine
Desai, Dhimant,Lin, Guoying,Morimoto, Hiromi,Williams, Philip G.,El-Bayoumy, Karam,Amin, Shantu
, p. 1133 - 1141 (2002)
Tobacco-specific N′-nitrosamines (TSNA) ...
The first enantioselective synthesis of (S)-5-bromo-3-(1-methyl-2-pyrrolidinyl) pyridine: a key intermediate for the preparation of SIB-1508Y
FX Felpin, G Vo-Thanh, J Villiéras, J Lebreton
, (2021/08/27)
Starting from 5-bromo-3-pyridinecarboxaldehyde 10, the racemic alcohol 11 was prepared by allylation with allyl bromide in the presence of zinc in 97% yield after purification by flash …
A catalytic oxidation heterocyclic aromatic primary alcohol for the preparation of heterocyclic aromatic aldehyde
-
Paragraph 0023-0026, (2019/05/04)
The invention provides a method for prep...
Synthesis of (plus or minus)[5-{sup 3} H] N'-Nitrosoanatabine, a tobacco-specific nitrosamine
S Amin
Journal of Labelled Compounds and Radiopharmaceuticals, 2002
The starting material, 5-bromo-3-pyridinecarboxaldehyde, was condensed with ethylcarbamate to give compound 2 in quantitative yield. Diels-Alder reaction of compound 2 with 1,3-…
Efficient synthesis of chromone and flavonoid derivatives with diverse heterocyclic units
MA Arai, M Sato, K Sawada, T Hosoya
Chemistry – An Asian Journal, Volume3, Issue12 December 1, 2008
After formation of chalcone, 5-bromo-3-pyridinecarboxaldehyde (2 d) (104 mg, 0.56 mmol) was added to the reaction mixture, which was then stirred at 40 C for 2 h, quenched by …
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