155790-12-8 Usage
Description
6-methyl-2-(methylamino)nicotinic acid is a chemical compound with the molecular formula C8H10N2O2, belonging to the class of nicotinic acid derivatives, which are forms of vitamin B3. 6-methyl-2-(methylamino)nicotinic acid features a methyl group and a methylamino group attached to the nicotinic acid structure, endowing it with potential biological activities and applications in pharmaceutical synthesis and medicine.
Uses
Used in Pharmaceutical Synthesis:
6-methyl-2-(methylamino)nicotinic acid is utilized as a key intermediate in the synthesis of various pharmaceuticals, leveraging its unique structural features to contribute to the development of new drugs and therapeutic agents.
Used in Medicinal Applications:
In the field of medicine, 6-methyl-2-(methylamino)nicotinic acid is studied for its potential biological activities, such as antioxidant, anti-inflammatory, and neuroprotective properties, which may contribute to the treatment and management of various diseases and conditions.
Used in Drug Development:
6-methyl-2-(methylamino)nicotinic acid serves as a building block in drug development, providing a foundation for the creation of innovative and effective medications that can address unmet medical needs and improve patient outcomes across different therapeutic areas.
Check Digit Verification of cas no
The CAS Registry Mumber 155790-12-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,5,5,7,9 and 0 respectively; the second part has 2 digits, 1 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 155790-12:
(8*1)+(7*5)+(6*5)+(5*7)+(4*9)+(3*0)+(2*1)+(1*2)=148
148 % 10 = 8
So 155790-12-8 is a valid CAS Registry Number.
155790-12-8Relevant articles and documents
Iridium-catalyzed enantioselective addition of an: N -methyl C-H bond to α-trifluoromethylstyrenes via C-H activation
Yamauchi, Daisuke,Nakamura, Ikumi,Nishimura, Takahiro
supporting information, p. 11787 - 11790 (2021/11/30)
The Ir-catalyzed enantioselective addition of an N-methyl C-H bond of 2-(methylamino)pyridine derivatives to α-trifluoromethylstyrenes proceeded via C-H activation to give chiral γ-branched amine derivatives having a trifluoromethyl-substituted stereocenter. It was found that a bulky and electron-withdrawing group at the 3-position of 2-(methylamino)pyridines was necessary for the present C-H addition reaction catalyzed by a cationic iridium/chiral bisphosphine complex.
SYNTHESIS OF THE MUTAGENIC 2-AMINO-1,6-DIMETHYLIMIDAZOPYRIDINE (1,6-DMIP) AND FIVE OF ITS ISOMERS
Lindstroem, Stefan,Ahmad, Tania,Grivas, Spiros
, p. 529 - 540 (2007/10/02)
Synthetic routes to 2-amino-1,6-dimethylimidazopyridine and its 1,5-, 1,7-, 3,5- 3,6- and 3,7-dimethyl isomers from methyl derivatives of 3-hydroxy- or 2-amino-pyridine and 2-chloronicotinic acid are described.
