251801
乙酰基吡嗪
97%
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关于此项目
经验公式（希尔记法）:
C6H6N2O
化学文摘社编号:
分子量:
122.12
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
244-753-5
Beilstein/REAXYS Number:
109630
MDL number:
Assay:
97%
Form:
solid
产品名称
乙酰基吡嗪, 97%
InChI key
DBZAKQWXICEWNW-UHFFFAOYSA-N
InChI
1S/C6H6N2O/c1-5(9)6-4-7-2-3-8-6/h2-4H,1H3
SMILES string
CC(=O)c1cnccn1
assay
97%
form
solid
mp
76-78 °C (lit.)
functional group
ketone
Quality Level
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Application
Acetylpyrazine has been used in synthesis of:
- 7-heteroaryl-pyrazolo[1,5-a]pyrimidine-3-carboxamides
- copper (II) complexes with di-imine ligands
- N(4) substituted thiosemicarbazones
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 2
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
dust mask type N95 (US), Eyeshields, Gloves
Sizana Ahmetaj et al.
Molecular diversity, 17(4), 731-743 (2013-08-27)
A simple and practical four-step protocol for the parallel synthesis of 7-heteroaryl-pyrazolo[1,5-[Formula: see text]]pyrimidine-3-carboxamides was developed. The synthesis starts with transformation of commercially available 2-acetylpyridine and acetylpyrazine with [Formula: see text] [Formula: see text]-dimethylformamide dimethylacetal into the corresponding [Formula: see
Spectroscopic characterization of schiff base-copper complexes immobilized in smectite clays.
Dias PM, et al.
Quimica nova, 33(10), 2135-2142 (2010)
Cobalt (III) complexes of formyl-and acetylpyrazine N (4)-substituted thiosemicarbazones.
West DX, et al.
Transition Met. Chem. (London), 22(5), 447-452 (1997)
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