4,7-Epoxy-1H-isoindole-1,3(2H)-dione,hexahydro-4,7-dimethyl-2-(2-thiazolyl)

Modify Date: 2025-09-23 19:01:45

4,7-Epoxy-1H-isoindole-1,3(2H)-dione,hexahydro-4,7-dimethyl-2-(2-thiazolyl) Structure
4,7-Epoxy-1H-isoindole-1,3(2H)-dione,hexahydro-4,7-dimethyl-2-(2-thiazolyl) structure
Common Name 4,7-Epoxy-1H-isoindole-1,3(2H)-dione,hexahydro-4,7-dimethyl-2-(2-thiazolyl)
CAS Number 19783-63-2 Molecular Weight 278.32700
Density 1.457g/cm3 Boiling Point 410.4ºC at 760mmHg
Molecular Formula C13H14N2O3S Melting Point N/A
MSDS N/A Flash Point 202ºC

 Names

Name 4,7-dimethyl-2-(1,3-thiazol-2-yl)-3a,5,6,7a-tetrahydro-octahydro-1H-4,7-epoxyisoindole-1,3-dione
Synonym More Synonyms

 Chemical & Physical Properties

Density 1.457g/cm3
Boiling Point 410.4ºC at 760mmHg
Molecular Formula C13H14N2O3S
Molecular Weight 278.32700
Flash Point 202ºC
Exact Mass 278.07300
PSA 87.74000
LogP 1.65510
Vapour Pressure 6.02E-07mmHg at 25°C
Index of Refraction 1.637
InChIKey WESNUVHBKHZVAG-UHFFFAOYSA-N
SMILES CC12CCC(C)(O1)C1C(=O)N(c3nccs3)C(=O)C12

 Precursor & DownStream

Precursor  2

DownStream  0

 Bioassay

View more

Name: Luminescence-based cell-based primary high throughput screening assay to identify ago...
Source: The Scripps Research Institute Molecular Screening Center
Target: mu-type opioid receptor isoform MOR-1 [Homo sapiens]
External Id: OPRM1-OPRD1_AG_LUMI_1536_1X%ACT PRUN
Name: QFRET-based biochemical primary high throughput screening assay to identify exosite i...
Source: The Scripps Research Institute Molecular Screening Center
Target: disintegrin and metalloproteinase domain-containing protein 17 preproprotein [Homo sapiens]
External Id: ADAM17_INH_QFRET_1536_1X%INH PRUN
Name: Fluorescence-based cell-based primary high throughput screening assay to identify ago...
Source: The Scripps Research Institute Molecular Screening Center
Target: muscarinic acetylcholine receptor M1 [Homo sapiens]
External Id: CHRM1_AG_FLUO8_1536_1X%ACT PRUN
Name: qHTS for Inhibitors of human tyrosyl-DNA phosphodiesterase 1 (TDP1): qHTS in cells in...
Source: NCGC
Target: TDP1 protein [Homo sapiens]
External Id: TDP1100
Name: qHTS for Inhibitors of human tyrosyl-DNA phosphodiesterase 1 (TDP1): qHTS in cells in...
Source: NCGC
Target: TDP1 protein [Homo sapiens]
External Id: TDP1101
Name: Schnurri-3 Inhibitors: specific inducers of adult bone formation Measured in Cell-Bas...
Source: Broad Institute
Target: N/A
External Id: 2134-01_Inhibitor_SinglePoint_HTS_Activity_Set2
Name: Fluorescence polarization to screen for inhibitor that competite the binding of FadD2...
Source: Broad Institute
Target: FATTY-ACID-CoA LIGASE FADD28 (FATTY-ACID-CoA SYNTHETASE)
External Id: 2147-01_Inhibitor_SinglePoint_HTS_Activity
Name: Bursicon-induced LGR2 mediated cAMP production in LGR-2/CRE6x-Luciferase co-transfect...
Source: Broad Institute
Target: N/A
External Id: Bursicon-induced LGR2 mediated cAMP production in LGR-2/CRE6x-Luciferase co-transfected HEK293 cells Inhibition - 7011-01_Antagonist_SinglePoint_HTS_Activity
Name: High throughput screen for small molecule inhibitors of a hypoxia-regulated fluoresce...
Source: ICCB-Longwood/NSRB Screening Facility, Harvard Medical School
Target: N/A
External Id: HMS1149-MLP
Name: qHTS for Inhibitors of AMA1-RON; Towards Development of Antimalarial Drug Lead: Prima...
Source: NCGC
Target: apical membrane antigen 1, AMA1 [Plasmodium falciparum 3D7]
External Id: AMA1100
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 Synonyms

4,7-dimethyl-2-thiazol-2-yl-hexahydro-4,7-epioxido-isoindole-1,3-dione
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