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About This Item
Empirical Formula (Hill Notation):
C5H5N3O2
CAS Number:
Molecular Weight:
139.11
Beilstein/REAXYS Number:
124835
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22
Recommended Products
assay
≥99%
form
powder
mp
205-210 °C (dec.) (lit.)
SMILES string
Nc1nccnc1C(O)=O
InChI
1S/C5H5N3O2/c6-4-3(5(9)10)7-1-2-8-4/h1-2H,(H2,6,8)(H,9,10)
InChI key
ZAGZIOYVEIDDJA-UHFFFAOYSA-N
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signalword
Danger
hcodes
Hazard Classifications
Eye Dam. 1
Storage Class
11 - Combustible Solids
wgk_germany
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
dust mask type N95 (US), Eyeshields, Gloves
Certificates of Analysis (COA)
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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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