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88912-27-0

88912-27-0 Structure

88912-27-0 Structure
IdentificationMore
[Name]

3-Chloroisonicotinic acid
[CAS]

88912-27-0
[Synonyms]

3-CHLORO-4-PYRIDINECARBOXYLIC ACID
3-CHLOROISONICOTINIC ACID
3-CHLOROPYRIDINE-4-CARBOXYLIC ACID
3-Chloro-4-pyridine carboxlic acid
3-Chloro-4-pyridinecarboxylic acid, 3-Chloroisonicotinic acid
[Molecular Formula]

C6H4ClNO2
[MDL Number]

MFCD03094685
[Molecular Weight]

157.55
[MOL File]

88912-27-0.mol
Chemical PropertiesBack Directory
[Melting point ]

227-231 °C (dec.)(lit.)
[Boiling point ]

387.0±22.0 °C(Predicted)
[density ]

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

Inert atmosphere,Room Temperature
[form ]

Solution
[pka]

0.12±0.25(Predicted)
[color ]

Brown to dark green to black
[InChIKey]

MYAZXWFEMDJTFE-UHFFFAOYSA-N
[CAS DataBase Reference]

88912-27-0(CAS DataBase Reference)
Safety DataBack Directory
[Hazard Codes ]

Xn,Xi
[Risk Statements ]

R22:Harmful if swallowed.
[Safety Statements ]

S36:Wear suitable protective clothing .
[WGK Germany ]

3
[Hazard Note ]

Irritant
[HazardClass ]

IRRITANT
[HS Code ]

29333999
Spectrum DetailBack Directory
[Spectrum Detail]

3-Chloroisonicotinic acid(88912-27-0)1HNMR
Well-known Reagent Company Product InformationBack Directory
[Sigma Aldrich]

88912-27-0(sigmaaldrich)
Hazard InformationBack Directory
[Synthesis]

3-Chloropyridine

626-60-8

3-Chloroisonicotinic acid

88912-27-0

A. Synthesis of 3-chloro-N-(4-chlorophenyl)pyridine-4-carboxamide. At -78 °C, 3-chloropyridine (1.00 mL, 10.5 mmol) was dissolved in THF and a freshly prepared lithium diisopropylammonium THF solution [prepared by the reaction of butyl lithium (7.21 mL, 11.5 mmol) with diisopropylamine (11.5 mmol)] was slowly added. After 0.25 h of reaction, carbon dioxide gas was passed into the mixture and slowly warmed to room temperature. After completion of the reaction, the mixture was concentrated and subsequently partitioned between EtOAc and water. The aqueous layer was washed twice with EtOAc. The pH of the aqueous layer was adjusted to about 3 by adding 1N HCl and extracted three more times with EtOAc. The organic phases were combined, dried with magnesium sulfate and concentrated. The residue was recrystallized by EtOAc to give 200 mg (12% yield) of 3-chloroisonicotinic acid.

[References]

[1] Patent: US6610704, 2003, B1
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