2,5-Pyridinedicarboxylic acid

Names

[ CAS No. ]:
100-26-5

[ Name ]:
2,5-Pyridinedicarboxylic acid

[Synonym ]:
2,5-Pyridinedicarboxylic Acid
6-carboxy-nicotinic acid
2,4-DIOXO-1,2,3,4-TETRAHYDROQUINAZOLINE-7-CARBOXAMIDE
ICA
2,5-LUTIDINIC ACID
Isocinchomeronic Acid
ISOCINCHOMERIC ACID
pyridine-2,5-dicarboxylic acid
EINECS 202-834-2
PYRIDINEDICARBOXYLIC ACID
RARECHEM AL BO 2394
Isochincomerionicacid
2,5-PYRIDINECARBOXYLIC ACID
2,5-di-carboxy-pyridine
MFCD00006297
pyridine2,5-dicarboxylate

Biological Activity

[Description]:

2,5-Pyridinedicarboxylic acid is a biochemical reagent that can be used as a biological material or organic compound for life science related research.

[Related Catalog]:

Research Areas >> Others

[In Vitro]

2,5-吡啶二羧酸用于制备作为抗病毒剂的新衍生物。

Chemical & Physical Properties

[ Density]:
1.6±0.1 g/cm3

[ Boiling Point ]:
441.1±30.0 °C at 760 mmHg

[ Melting Point ]:
242-247 °C (dec.)(lit.)

[ Molecular Formula ]:
C₇H₅NO₄

[ Molecular Weight ]:
167.12

[ Flash Point ]:
220.5±24.6 °C

[ Exact Mass ]:
167.021851

[ PSA ]:
87.49000

[ LogP ]:
-0.25

[ Vapour Pressure ]:
0.0±1.1 mmHg at 25°C

[ Index of Refraction ]:
1.628

MSDS

Click to get detail MSDS

Safety Information

[ Symbol ]:

GHS07

[ Signal Word ]:
Warning

[ Hazard Statements ]:
H315-H319-H335

[ Precautionary Statements ]:
P261-P305 + P351 + P338

[ Personal Protective Equipment ]:
dust mask type N95 (US);Eyeshields;Gloves

[ Hazard Codes ]:
Xi:Irritant;

[ Risk Phrases ]:
R36/37/38

[ Safety Phrases ]:
S26-S36

[ RIDADR ]:
NONH for all modes of transport

[ WGK Germany ]:
3

[ HS Code ]:
2933399090

Synthetic Route

Click to get detail synthetic route

Precursor & DownStream

Precursor

DownStream

Customs

[ HS Code ]: 2933399090

[ Summary ]:
2933399090. other compounds containing an unfused pyridine ring (whether or not hydrogenated) in the structure. VAT:17.0%. Tax rebate rate:13.0%. . MFN tariff:6.5%. General tariff:20.0%

Articles

Identifying chelators for metalloprotein inhibitors using a fragment-based approach.

J. Med. Chem. 54 , 591-602, (2011)

Fragment-based lead design (FBLD) has been used to identify new metal-binding groups for metalloenzyme inhibitors. When screened at 1 mM, a chelator fragment library (CFL-1.1) of 96 compounds produced...

Competitive inhibitors of the CphA metallo-beta-lactamase from Aeromonas hydrophila.

Antimicrob. Agents Chemother. 51 , 2136-42, (2007)

Various inhibitors of metallo-beta-lactamases have been reported; however, none are effective for all subgroups. Those that have been found to inhibit the enzymes of subclass B2 (catalytically active ...

Inhibitor scaffolds for 2-oxoglutarate-dependent histone lysine demethylases.

J. Med. Chem. 51 , 7053-6, (2008)

The dynamic methylation of histone lysyl residues plays an important role in biology by regulating transcription, maintaining genomic integrity, and by contributing to epigenetic effects. Here we desc...