540234
2,5-吡啶二甲酸二甲酯
97%
别名:
甲基 6-甲氧羰基烟酸
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关于此项目
经验公式（希尔记法）:
C9H9NO4
化学文摘社编号:
分子量:
195.17
NACRES:
NA.22
PubChem Substance ID:
UNSPSC Code:
12352100
MDL number:
Assay:
97%
InChI
1S/C9H9NO4/c1-13-8(11)6-3-4-7(10-5-6)9(12)14-2/h3-5H,1-2H3
SMILES string
COC(=O)c1ccc(nc1)C(=O)OC
InChI key
TUGSJNQAIMFEDY-UHFFFAOYSA-N
assay
97%
mp
213-217 °C (lit.)
functional group
ester
Quality Level
General description
Dimethyl 2,5-pyridine dicarboxylate can be prepared from 2,5-pyridinedicarboxylic acid.
Application
Dimethyl 2,5-pyridine dicarboxylate (Dimethyl 2,5-pyridinedicarboxylate) may be used in the synthesis of:
- 2,5-dicarbomethoxy-N-methylpyridinium methosulfate
- 2,5-dicarboxy-N-methylpyridinium betaine
- 6-carbomethoxy-2-carboxypyridine-N-oxide
signalword
Warning
hcodes
Hazard Classifications
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
target_organs
Respiratory system
存储类别
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
dust mask type N95 (US), Eyeshields, Gloves
Nitrogen-Substituted Derivatives of 2, 5-Pyridinedicarboxylic Acid.
Peterson ML.
The Journal of Organic Chemistry, 25(4), 565-569 (1960)
Marta Soler et al.
Inorganic chemistry, 54(22), 10542-10558 (2015-10-28)
The conjugation of redox-active complexes that can function as chemical nucleases to cationic tetrapeptides is pursued in this work in order to explore the expected synergistic effect between these two elements in DNA oxidative cleavage. Coordination complexes of biologically relevant
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