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4-Chloropyridine-3-carboxaldehyde

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Products Intro: Product Name:4-Chloropyridine-3-carboxaldehyde
CAS:114077-82-6
Purity:98% Package:25kg
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CAS:114077-82-6
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Products Intro: Product Name:4-Chloro-3-pyridinecarboxaldehyde
CAS:114077-82-6
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4-Chloropyridine-3-carboxaldehyde manufacturers

4-Chloropyridine-3-carboxaldehyde Basic information
Product Name:4-Chloropyridine-3-carboxaldehyde
Synonyms:4-CHLOROPYRIDINE-3-CARBOXALDEHYDE;4-CHLORO-3-FORMYLPYRIDINE;3-Pyridinecarboxaldehyde,4-chloro-(9CI);4-chloro-3-pyridincarboxaldehyde;4-Chloro-3-pyridinecarboxaldehyde;4-chloropyridin-3-carbaldehyde;4-Chloro-pyridine-3-carbaldehyde/4- Chloronicotinaldehyde;4-chloro-3-pyridinecarbaldehyde
CAS:114077-82-6
MF:C6H4ClNO
MW:141.56
EINECS:
Product Categories:Pyridines;pyridine series;PYRIDINE;Building Blocks;Heterocycle-Pyridine series
Mol File:114077-82-6.mol
4-Chloropyridine-3-carboxaldehyde Structure
4-Chloropyridine-3-carboxaldehyde Chemical Properties
Boiling point 228.8±20.0 °C(Predicted)
density 1.332±0.06 g/cm3(Predicted)
storage temp. Inert atmosphere,Store in freezer, under -20°C
pka1.89±0.10(Predicted)
form solid
color Pale yellow
InChIInChI=1S/C6H4ClNO/c7-6-1-2-8-3-5(6)4-9/h1-4H
InChIKeyDYRMBQRXOMOMNW-UHFFFAOYSA-N
SMILESC1=NC=CC(Cl)=C1C=O
Safety Information
Hazard Codes Xn
Risk Statements 22-36-43
Safety Statements 26-36/37
HS Code 2933399990
MSDS Information
4-Chloropyridine-3-carboxaldehyde Usage And Synthesis
Chemical PropertiesWhite to light yellow powder
Synthesis
4-chloropyridine

626-61-9

N,N-Dimethylformamide

68-12-2

4-Chloropyridine-3-carboxaldehyde

114077-82-6

General procedure: a tetrahydrofuran solution (50 ml) of 4-chloropyridine (25.0 g, 0.22 mol) was slowly added dropwise to a solution of diisopropylammonium lithium prepared from a hexane solution of 1.6 M n-butyllithium (179 ml, 0.29 mol) with diisopropylamine (33.4 g, 0.33 mol) in tetrahydrofuran (300 ml) under the protection of argon gas, keeping the reaction temperature at -78°C. After dropwise addition, stirring was continued for 30 min. Subsequently, N,N-dimethylformamide (DMF, 19.3 g, 0.26 mol) was added and the reaction mixture was gradually warmed up to room temperature. After completion of the reaction, extraction was carried out with ethyl acetate (200 ml) and 5% aqueous ammonium chloride solution (300 ml). The organic layer was separated, dried with anhydrous magnesium sulfate and concentrated under reduced pressure to remove the solvent to give the crude product 4-chloro-3-pyridinecarboxaldehyde (27 g, 86% yield) as an oil. The product was characterized by 1H-NMR (200 MHz, CDCl3): δ 7.45 (1H, d, J = 5.0 Hz), 8.69 (1H, d, J = 5.0 Hz), 9.05 (1H, s), 10.51 (1H, s).

References[1] Patent: EP1348706, 2003, A1. Location in patent: Page/Page column 37
[2] Patent: US2011/53975, 2011, A1. Location in patent: Page/Page column 60
[3] Journal of the American Chemical Society, 2013, vol. 135, # 40, p. 14916 - 14919
[4] Patent: WO2018/152329, 2018, A1. Location in patent: Page/Page column 44
[5] Patent: WO2004/41806, 2004, A2. Location in patent: Page 88-89
4-Chloropyridine-3-carboxaldehyde Preparation Products And Raw materials
Raw materialsEthyl acetate-->Methanol-->Tetrahydrofuran-->Sodium-->Sodium sulfate-->n-Butyllithium-->Nitrogen-->Ethyl formate-->Diisopropylamine-->4-Chloropyridinium chloride
Preparation Products4-Chloro-3-difluoromethyl-pyridine
Tag:4-Chloropyridine-3-carboxaldehyde(114077-82-6) Related Product Information
Chlorosulfonyl isocyanate Pentachloropyridine MCPA SODIUM N-Chlorosuccinimide 2-Chloro-5-chloromethylpyridine 3-Aminopyridine Clopidol 2-Chloro-3-cyanopyridine 3-Hydroxypyridine 4-Chloropyridinium chloride 4-CHLORO-1,3-DIMETHYLPYRAZOLO[3,4-B]PYRIDINE-5-CARBOXYLIC ACID 4-Chloronicotinic acid ETHYL 4-CHLORO-1,3-DIMETHYL-1H-PYRAZOLO[3,4-B]PYRIDINE-5-CARBOXYLATE 4-CHLORO-1,3-DIMETHYLPYRAZOLO[3,4-B]PYRIDINE-5-CARBONYL CHLORIDE 5-CHLORO-2-FORMYLPYRIDINE 5-Chloropyridine-3-carboxaldehyde 3-CHLOROISONICOTINALDEHYDE 2-CHLOROPYRIDINE-3-CARBOXALDEHYDE,2-Chloropyridine-3-carboxaldehyde, 2-Chloro-3-formylpyridine