6-METHYLPYRIDINE-2-CARBOXYLIC ACID

CC1=CC=CC(=N1)C(O)=O

InChIKey=LTUUGSGSUZRPRV-UHFFFAOYSA-N

InChI=1S/C7H7NO2/c1-5-3-2-4-6(8-5)7(9)10/h2-4H,1H3,(H,9,10)

Stereochemistry	ACHIRAL
Additional Stereochemistry	No
Defined Stereocenters	0 / 0
E/Z Centers	0
Optical Activity	NONE

PubMed

Title	Date	PubMed
Efficient energy conversion in photochromic ruthenium DMSO complexes.	2006 Jul 24	16842000
A one-dimensional CdII coordination polymer: catena-poly[cadmium(II)-bis(mu-6-methylpicolinato)].	2007 Sep	17762103
Interactions of insulin-mimetic zinc(II) complexes with cell constituents: glutathione and ATP.	2008 Jul	18282604
Tuning the coordination sphere around highly luminescent lanthanide complexes.	2008 May 5	18393412
Bioconversion of 2,6-dimethylpyridine to 6-methylpicolinic acid by Exophiala dermatitidis (Kano) de Hoog DA5501 cells grown on n-dodecane.	2010 Apr	20082073
A quantitative study of the biotransformation of insulin-enhancing VO(2+) compounds.	2010 Aug	20339887

Patents

Substance Class	Chemical Created by `admin` on `Fri Dec 15 19:09:07 GMT 2023` Edited by `admin` on `Fri Dec 15 19:09:07 GMT 2023`
Record UNII	KB675Y352L
Record Status	`Validated (UNII)`
Record Version

Name

Type

Language

6-METHYLPYRIDINE-2-CARBOXYLIC ACID

Systematic Name

English

PICOLINIC ACID, 6-METHYL-

Common Name

English

2-PYRIDINECARBOXYLIC ACID, 6-METHYL-

Common Name

English

2-CARBOXY-6-METHYLPYRIDINE

Systematic Name

English

6-METHYLPICOLINIC ACID

Systematic Name

English

6-METHYL-2-PYRIDINECARBOXYLIC ACID

Systematic Name

English

NSC-26023

Code

English

2-PICOLINE-6-CARBOXYLIC ACID

Common Name

English

Code System Code Type Description

EPA CompTox

DTXSID20239416