A76982
3-氨基吡嗪-2-羧酸
≥99%
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关于此项目
经验公式（希尔记法）:
C5H5N3O2
化学文摘社编号:
分子量:
139.11
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
226-558-7
Beilstein/REAXYS Number:
124835
MDL number:
产品名称
3-氨基吡嗪-2-羧酸, ≥99%
InChI key
ZAGZIOYVEIDDJA-UHFFFAOYSA-N
InChI
1S/C5H5N3O2/c6-4-3(5(9)10)7-1-2-8-4/h1-2H,(H2,6,8)(H,9,10)
SMILES string
Nc1nccnc1C(O)=O
assay
≥99%
form
powder
mp
205-210 °C (dec.) (lit.)
Quality Level
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signalword
Danger
hcodes
Hazard Classifications
Eye Dam. 1
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
法规信息
新产品
此项目有
A J Dobson et al.
Acta crystallographica. Section C, Crystal structure communications, 52 ( Pt 6), 1512-1514 (1996-06-15)
3-Aminopyrazine-2-carboxylic acid, C5H5N3O2, displays an extensive network of intra- and intermolecular hydrogen bonds which are undoubtedly responsible for the modest values of the displacement parameters. H-atom transfer to the ring N atoms did not occur and the carboxy and amino
Ghada Bouz et al.
Molecules (Basel, Switzerland), 24(7) (2019-03-31)
We report the design, synthesis, and in vitro antimicrobial activity of a series of N-substituted 3-aminopyrazine-2-carboxamides with free amino groups in position 3 on the pyrazine ring. Based on various substituents on the carboxamidic moiety, the series is subdivided into
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