| Identification | More | [Name]
2-Chloro-3-pyridinecarboxaldehyde | [CAS]
36404-88-3 | [Synonyms]
2-CHLORO-3-FORMYLPYRIDINE
2-CHLORO-3-PYRIDINECARBOXALDEHYDE
2-CHLORONICOTINALDEHYDE
2-CHLORO-PYRIDIN-3-CARBALDEHYDE
2-CHLORO-PYRIDINE-3-CARBALDEHYDE
2-CHLOROPYRIDINE-3-CARBOXALDEHYDE
CHLORO-2-FORMYL-3-PYRIDINE
TIMTEC-BB SBB004156
2-CHLORO-PYRIDINE-3-CARBALDEHYDE 97+%
2-Chloropyridine-3-carboxaldehyde, 2-Chloro-3-formylpyridine
2-Chloro-3-pyridylcarboxaldehyde
3-Pyridinecarboxaldehyde, 2-chloro- | [Molecular Formula]
C6H4ClNO | [MDL Number]
MFCD01315308 | [Molecular Weight]
141.56 | [MOL File]
36404-88-3.mol |
| Chemical Properties | Back Directory | [Melting point ]
50-54 °C (lit.) | [Boiling point ]
119 °C(Press: 30 Torr) | [density ]
1.332±0.06 g/cm3(Predicted) | [Fp ]
>230 °C
| [storage temp. ]
Keep in dark place,Sealed in dry,Room Temperature | [solubility ]
Chloroform, DMSO | [form ]
Powder or Low Melting Solid | [pka]
-1.36±0.10(Predicted) | [color ]
White to off-white | [Detection Methods]
HPLC,NMR | [InChI]
InChI=1S/C6H4ClNO/c7-6-5(4-9)2-1-3-8-6/h1-4H | [InChIKey]
KHPAGGHFIDLUMB-UHFFFAOYSA-N | [SMILES]
C1(Cl)=NC=CC=C1C=O | [CAS DataBase Reference]
36404-88-3(CAS DataBase Reference) | [Storage Precautions]
Store under nitrogen |
| Safety Data | Back Directory | [Hazard Codes ]
Xn,Xi | [Risk Statements ]
R22:Harmful if swallowed.
R36:Irritating to the eyes.
R43:May cause sensitization by skin contact. | [Safety Statements ]
S26:In case of contact with eyes, rinse immediately with plenty of water and seek medical advice .
S36/37:Wear suitable protective clothing and gloves . | [WGK Germany ]
3
| [HazardClass ]
IRRITANT | [HS Code ]
29333990 | [Storage Class]
11 - Combustible Solids | [Hazard Classifications]
Acute Tox. 4 Oral
Eye Irrit. 2
Skin Sens. 1 |
| Hazard Information | Back Directory | [Chemical Properties]
Brown Solid | [Uses]
Starting material for the preparation of 5-azaindoles by the Hemetsberger-Knittel reaction involving the thermal decomposition of alkenyl azides. | [Uses]
Azaindazole intermediate. | [Uses]
Starting material for the preparation of 5-azaindoles by the Hemetsberger-Knittel reaction involving the thermal decomposition of alkenyl azides.1 | [Synthesis]
General procedure for the synthesis of 2-chloro-3-pyridinecarboxaldehyde from 2-chloro-3-pyridinemethanol: The hydrolyzed product was transferred to a four-necked flask, 300 g of ethyl acetate and 0.8 g of TEMPO were added, and the mixture was stirred and cooled to 0 °C. Subsequently, 450 g of freshly prepared sodium hypochlorite solution (pH=11, 10% active chlorine) was slowly added dropwise, and the reaction temperature was controlled at 0-5 °C. After the dropwise addition, the reaction system was warmed up to room temperature and stirred continuously for 1 hour to ensure complete reaction. Post-treatment steps: the reaction mixture was allowed to stand and layered, the ethyl acetate phase was separated, washed with water, dried with anhydrous magnesium sulfate, concentrated and then cooled and crystallized to give 79 g of the light yellow crystalline product 2-chloro-3-pyridinecarboxaldehyde, with a purity of 98.2%, and based on the yield of 2-chloro-3-chloromethylpyridine was 89.6%. | [References]
[1] Patent: CN107501171, 2017, A. Location in patent: Paragraph 0028; 0034; 0035; 0036; 0037; 0044; 0045-0047
[2] Journal of Heterocyclic Chemistry, 1995, vol. 32, # 5, p. 1595 - 1597
[3] Synthetic Communications, 2008, vol. 38, # 6, p. 889 - 904
[4] Synthesis, 2010, # 20, p. 3439 - 3448
[5] Chemical and Pharmaceutical Bulletin, 2000, vol. 48, # 5, p. 694 - 707 |
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