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:
grade
technical
assay
≥90% (NT)
impurities
≤3% water
mp
85-92 °C
SMILES string
Nc1nccs1
InChI
1S/C3H4N2S/c4-3-5-1-2-6-3/h1-2H,(H2,4,5)
InChI key
RAIPHJJURHTUIC-UHFFFAOYSA-N
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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B Michael Silber et al.
Pharmaceutical research, 30(4), 932-950 (2013-02-19)
To discover drugs lowering PrP(Sc) in prion-infected cultured neuronal cells that achieve high concentrations in brain to test in mouse models of prion disease and then treat people with these fatal diseases. We tested 2-AMT analogs for EC50 and PK
Samantha Leone et al.
Bioorganic & medicinal chemistry, 16(10), 5695-5703 (2008-04-15)
REST/NRSF is a multifunctional transcription factor that represses or silences many neuron-specific genes in both neural and non-neural cells by recruitment to its cognate RE1/NRSE regulatory sites. An increase in RE1/NRSE genomic binding is found in Huntington's disease (HD), resulting
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
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
Global Trade Item Number
| SKU | GTIN |
|---|---|
| V659-10G | 04061835283330 |
| V659-100G | 04054839595394 |
| V659-25G | 04061835283347 |
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