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关于此项目
经验公式(希尔记法):
C7H7N3
化学文摘社编号:
分子量:
133.15
NACRES:
NA.22
PubChem Substance ID:
UNSPSC Code:
12352100
EC Number:
242-971-5
MDL number:
产品名称
5-氨基吲唑, 97%
assay
97%
form
solid
InChI key
XBTOSRUBOXQWBO-UHFFFAOYSA-N
InChI
1S/C7H7N3/c8-6-1-2-7-5(3-6)4-9-10-7/h1-4H,8H2,(H,9,10)
SMILES string
Nc1ccc2[nH]ncc2c1
mp
175-178 °C (lit.)
Quality Level
signalword
Danger
hcodes
Hazard Classifications
Acute Tox. 3 Oral - Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
target_organs
Respiratory system
存储类别
6.1C - Combustible acute toxic Cat.3 / toxic compounds or compounds which causing chronic effects
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Eyeshields, Faceshields, Gloves, type P2 (EN 143) respirator cartridges
Chai Hoon Soh et al.
Journal of combinatorial chemistry, 8(4), 464-468 (2006-07-11)
A microwave-assisted parallel synthesis of 2,4-disubstituted 5-aminoimidazoles has been developed. Significant rate enhancement was observed for all steps in the three-step protocol. The overall reaction time was shortened to 25 min, as compared to 53 h for the conventional procedures.
Ratika Krishnamurty et al.
Bioorganic & medicinal chemistry letters, 21(1), 550-554 (2010-11-17)
Affinity reagents that target protein kinases are powerful tools for signal transduction research. Here, we describe a general set of kinase ligands based on a 5-aminoindazole scaffold. This scaffold can readily be derivatized with diverse binding elements and immobilized analogs
Feng Shi et al.
Molecular diversity, 15(2), 497-505 (2010-09-04)
Six new series of pyrazolo[4,3-f]quinoline derivatives with potential bioactivities were synthesized by the three-component reactions of aromatic aldehydes, 5-aminoindazole, and various cyclic 1,3-dicarbonyl compounds under microwave irradiation. This protocol has the valuable features of structural diversity of products, broader substrate
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