CAS No.41667-95-2 | 5,6-Dichloronicotinic acid
Name: 5,6-Dichloronicotinic acid CAS No.41667-95-2 MF: C6H3Cl2NO2 MW: 192 Purity:97% Package: 5g,25g,100g,500g,1kg,25kg Worldwide Delivery
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Analytical Chemicals
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Product introduction
Introduction and application of CAS No.41667-95-2 | 5,6-Dichloronicotinic acid
5,6-Dichloronicotinic acid is a compound that can be synthesized by reacting methyl ketones with chloroacetic acid. It is used in the synthesis of maleic anhydride and has been shown to inhibit the catalysis of acetylcholine chloride. 5,6-Dichloronicotinic acid has also been shown to have an inhibitory effect on Alzheimer's disease. The kinetic mechanism for this inhibition occurs through the hydrolysis step of 5,6-Dichloronicotinic acid by magnesium chloride in hexane solution. The reactive acylation reaction proceeds when 5,6-Dichloronicotinic acid reacts with acetic anhydride in the presence of pyridine.
Synonyms:
5,6-DICHLORO-3-PYRIDINECARBOXYLICACID;
5,6-DICHLORONICOTINICACID;
5,6-DICHLOROPYRIDINE-3-CARBOXYLICACID;
5,6-Dichloropyridine-3-carboxylicacid;
5,6-Dichloro;
5,6-DICHLORONICOTINICACID98+%;
5,6-Dichloronicotinicacid,5,6-Dichloropyridine-3-carboxylicacid
Specification of CAS No.41667-95-2 | 5,6-Dichloronicotinic acid
|
ITEMS |
SPECIFICATION |
|
CAS No. |
41667-95-2 |
|
MF |
C6H3Cl2NO2 |
|
MW |
192 |
|
Boiling point |
342.1ºC at 760 mmHg |
|
Melting point |
164-168ºC |
|
Flashing point |
160.7ºC |
|
Density |
1.612 g/cm3 |
|
acidity coefficient(pKa) |
2.87±0.10(Predicted) |
|
refractive index |
1.605 |
Package of CAS No.41667-95-2 | 5,6-Dichloronicotinic acid
Package:100g; 500g; 1kg; 25kg;bulk package
Transportation: by courier/ by air/ by sea
Related Articles of CAS No.41667-95-2 | 5,6-Dichloronicotinic acid
Tetrahydroacridine derivatives with dichloronicotinic acid moiety as attractive, multipotent agents for Alzheimer's disease treatment
K Czarnecka, N Chufarova, K Halczuk… - European journal of …, 2018 - Elsevier
… A novel series of 9-amino-1,2,3,4-tetrahydroacridine and 5,6-dichloronicotinic acid moiety
were conjugated with different linkers. Afterwards new derivatives were evaluated as potential …
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