09480
2-Aminothiazol
technical, ≥90% (NT)
Synonym(s):
2-Thiazolamine
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About This Item
Empirical Formula (Hill Notation):
C3H4N2S
CAS Number:
Molecular Weight:
100.14
EC Number:
202-511-6
UNSPSC Code:
12352100
PubChem Substance ID:
Beilstein/REAXYS Number:
105738
MDL number:
InChI key
RAIPHJJURHTUIC-UHFFFAOYSA-N
InChI
1S/C3H4N2S/c4-3-5-1-2-6-3/h1-2H,(H2,4,5)
SMILES string
Nc1nccs1
grade
technical
assay
≥90% (NT)
impurities
≤3% water
mp
85-92 °C
signalword
Warning
hcodes
pcodes
Hazard Classifications
Acute Tox. 4 Oral
Storage Class
13 - Non Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
dust mask type N95 (US), Eyeshields, Faceshields, Gloves
Regulatory Information
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Qingping Zeng et al.
Bioorganic & medicinal chemistry letters, 20(5), 1652-1656 (2010-02-09)
A series of 2-aminothiadiazole of inhibitors of AKT1 is described. SAR relationships are discussed, along with selectivity for protein kinase A (PKA) and cyclin-dependent kinase 2 (CDK2). Moderate selectivity observed in several compounds for AKT1 versus PKA is rationalized by
Jiazhong Li et al.
Analytica chimica acta, 631(1), 29-39 (2008-12-03)
In this study, the quantitative structure-activity relationship (QSAR) of a series of 2-aminothiazole based Lck inhibitors was investigated. The key structural features responsible for the inhibition activities were discussed in detail. A population of 100 rigorously validated linear QSAR models
Strayo De et al.
Chemico-biological interactions, 173(3), 215-223 (2008-05-10)
Oceans are among the richest natural sources of many bioactive compounds. Several of these compounds have shown pharmacological activities for many diseases. Dendrodoine (5-[(3-N-dimethylamino)-1,2,4-thiadiazolyl]-3-indanyl methanone) is an alkaloid extracted from the marine tunicate Dendrodoa grossularia. Aminothiazoles have a wide range
Mari Kuramoto et al.
Organic & biomolecular chemistry, 6(15), 2772-2781 (2008-07-18)
A series of 2-(2-aminothiazol-4-yl)benzo[b]furan and 3-(2-aminothiazol-4-yl)benzo[b]furan derivatives were prepared, and their leukotriene B(4) inhibitory activity and growth inhibitory activity in cancer cell lines were evaluated. Several compounds showed strong inhibition of calcium mobilization in CHO cells overexpressing human BLT(1) and
Yusuke Oka et al.
Bioorganic & medicinal chemistry letters, 22(24), 7534-7538 (2012-11-06)
A novel series of 2-aminothiazole-oxazoles was designed and synthesized as part of efforts to develop potent phosphoinositide 3-kinase γ (PI3Kγ) inhibitors. The modification of a high-throughput screening hit, compound 1, resulted in the identification of compounds 10 and 15, which
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