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6313-54-8

6313-54-8 Structure

6313-54-8 Structure
IdentificationMore
[Name]

2-Chloro-4-pyridinecarboxylic acid
[CAS]

6313-54-8
[Synonyms]

2-CHLORO-4-PYRIDINECARBOXYLIC ACID
2-CHLORO-4-PYRIDINYL CARBOXYLIC ACID
2-CHLOROISONICOTINIC ACID
2-CHLOROPYRIDINE-4-CARBOXYLIC ACID
BUTTPARK 43\57-03
RARECHEM AL BO 0840
TIMTEC-BB SBB004003
2-Chloroisonicotinic
2-CHLOROPYRIDINE-4-CARBOXYLICACID(2-CHLOROISO-NICOTINICACID)
2-CHLORO-4-PYRIDINECARBOXYLIC ACID/2-CHLOROISONICOTINIC ACID
2-Chloroisonicotinic acid ,97%
4-Pyridinecarboxylic acid, 2-chloro-
[EINECS(EC#)]

613-143-4
[Molecular Formula]

C6H4ClNO2
[MDL Number]

MFCD00191402
[Molecular Weight]

157.55
[MOL File]

6313-54-8.mol
Chemical PropertiesBack Directory
[Appearance]

white crystall powder
[Melting point ]

246 °C (dec.)(lit.)
[Boiling point ]

417.7±25.0 °C(Predicted)
[density ]

1.470±0.06 g/cm3(Predicted)
[storage temp. ]

Keep in dark place,Sealed in dry,Room Temperature
[solubility ]

DMSO, Methanol
[form ]

Crystalline Powder
[pka]

3.00±0.10(Predicted)
[color ]

White to beige
[Detection Methods]

HPLC,NMR
[BRN ]

115861
[InChI]

InChI=1S/C6H4ClNO2/c7-5-3-4(6(9)10)1-2-8-5/h1-3H,(H,9,10)
[InChIKey]

QXCOHSRHFCHCHN-UHFFFAOYSA-N
[SMILES]

C1(Cl)=NC=CC(C(O)=O)=C1
[CAS DataBase Reference]

6313-54-8(CAS DataBase Reference)
Safety DataBack Directory
[Symbol(GHS) ]

Exclamation Mark (GHS07)
GHS07
[Signal word ]

Warning
[Hazard statements ]

H315-H319-H335
[Precautionary statements ]

P261-P264-P271-P280-P302+P352-P305+P351+P338
[Hazard Codes ]

Xi
[Risk Statements ]

R36/37/38:Irritating to eyes, respiratory system and skin .
[Safety Statements ]

S26:In case of contact with eyes, rinse immediately with plenty of water and seek medical advice .
S36:Wear suitable protective clothing .
S36/37/39:Wear suitable protective clothing, gloves and eye/face protection .
[RIDADR ]

UN2811
[WGK Germany ]

3
[Hazard Note ]

Irritant
[HazardClass ]

IRRITANT
[HS Code ]

29333990
[Storage Class]

11 - Combustible Solids
[Hazard Classifications]

Eye Irrit. 2
Skin Irrit. 2
STOT SE 3
Raw materials And Preparation ProductsBack Directory
[Raw materials]

Ethyl acetate-->Acetic acid-->Phosphorus oxitrichloride-->Hydrogen peroxide-->Isonicotinic acid-->2-Chloro-4-cyanopyridine
[Preparation Products]

2-Methoxypyridine-4-carboxaldehyde-->4-[4-(Aminomethyl)pyridin-2-yl]piperazine, N1-BOC protected-->(2-methoxypyridin-4-yl)methanol-->2-Morpholinoisonicotinaldehyde-->tert-Butyl 4-(4-cyanopyrid-2-yl)piperazine-1-carboxylate-->4-Amino-2-chloropyridine-->(2-Morpholinopyrid-4-yl)methanol-->2-[4-(tert-Butoxycarbonyl)piperazin-1-yl]isonicotinic acid-->2,2'-Bipyridine-4,4'-dicarboxylic acid-->Methyl 2-methoxyisonicotinate 97%methyl 2-methoxypyridine-4-carboxylate-->Methyl 2-chloroisonicotinate-->2-Chloropyridine-4-carbonyl chloride-->2-Piperazin-1-ylisonicotinic acid-->2-Morpholin-4-yl-isonicotinic acid-->Ethyl 2-Aminoisonicotinate-->2-Pyrrolidin-1-yl-isonicotinic acid hydrochloride-->2-Hydrazinoisonicotinic acid
Hazard InformationBack Directory
[Chemical Properties]

white crystall powder
[Uses]

Used in monocomposite films.
[Synthesis]

2-Chloro-4-cyanopyridine

33252-30-1

2-Chloro-4-pyridinecarboxylic acid

6313-54-8

General procedure for the synthesis of 2-chloroisonicotinic acid from 2-chloro-4-cyanopyridine: 2-chloro-4-cyanopyridine (2 mmol) was dissolved in 5 ml of [bmim]HSO4, and the reaction mixture was heated for 1-3 hours at 60-65 °C. The reaction process was monitored by thin layer chromatography (TLC). Upon completion of the reaction, the reaction mixture was poured into water containing crushed ice and the product precipitated as a precipitate. The precipitate was collected by filtration and dried. High yields (>90%) of 2-chloroisonicotinic acid were obtained in all reactions, and the products were sufficiently pure to require no further purification. The filtrate was concentrated under vacuum, washed twice with diethyl ether and concentrated again under high vacuum. After drying under reduced pressure, about 95% of the ionic liquid was recovered and compared to the original ionic liquid to verify its purity. The recovered ionic liquid showed no significant difference in efficiency of converting nitrile to acid compared to the original ionic liquid and could be reused 5-6 times without significant reduction in activity.

[References]

[1] Tetrahedron Letters, 2014, vol. 55, # 28, p. 3802 - 3804
[2] Roczniki Chemii, 1955, vol. 29, p. 1019,1025
[3] Chem.Abstr., 1956, p. 12045
Spectrum DetailBack Directory
[Spectrum Detail]

2-Chloro-4-pyridinecarboxylic acid(6313-54-8)MS
2-Chloro-4-pyridinecarboxylic acid(6313-54-8)1HNMR
2-Chloro-4-pyridinecarboxylic acid(6313-54-8)13CNMR
2-Chloro-4-pyridinecarboxylic acid(6313-54-8)IR1
2-Chloro-4-pyridinecarboxylic acid(6313-54-8)IR2
Well-known Reagent Company Product InformationBack Directory
[Acros Organics]

2-Chloroisonicotinic acid, 97%(6313-54-8)
[Alfa Aesar]

2-Chloropyridine-4-carboxylic acid, 98%(6313-54-8)
[Sigma Aldrich]

6313-54-8(sigmaaldrich)
[TCI AMERICA]

2-Chloroisonicotinic Acid,>98.0%(LC)(T)(6313-54-8)
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