2(1H)-Pyrimidinethione,3,4-dihydro-4,4,6-trimethyl-1-(4-nitrophenyl) structure
|
Common Name | 2(1H)-Pyrimidinethione,3,4-dihydro-4,4,6-trimethyl-1-(4-nitrophenyl) | ||
|---|---|---|---|---|
| CAS Number | 21038-75-5 | Molecular Weight | 277.34200 | |
| Density | 1.31g/cm3 | Boiling Point | 404.4ºC at 760mmHg | |
| Molecular Formula | C13H15N3O2S | Melting Point | N/A | |
| MSDS | N/A | Flash Point | 198.4ºC | |
| Name | 4,6,6-trimethyl-3-(4-nitrophenyl)-1H-pyrimidine-2-thione |
|---|---|
| Synonym | More Synonyms |
| Density | 1.31g/cm3 |
|---|---|
| Boiling Point | 404.4ºC at 760mmHg |
| Molecular Formula | C13H15N3O2S |
| Molecular Weight | 277.34200 |
| Flash Point | 198.4ºC |
| Exact Mass | 277.08800 |
| PSA | 93.18000 |
| LogP | 3.88870 |
| Vapour Pressure | 9.46E-07mmHg at 25°C |
| Index of Refraction | 1.655 |
| InChIKey | CPIHDWICCAVJDB-UHFFFAOYSA-N |
| SMILES | CC1=CC(C)(C)NC(=S)N1c1ccc([N+](=O)[O-])cc1 |
|
~87%
2(1H)-Pyrimidin... CAS#:21038-75-5 |
| Literature: Nasipuri, Dhanonjoy; Banerjee, Satinath; Alaka, B. V.; Daw, N. P. Synthesis, 1982 , # 12 p. 1073 - 1075 |
|
~69%
2(1H)-Pyrimidin... CAS#:21038-75-5 |
| Literature: Schmidt, Arthur H.; Russ, Manuel Chemische Berichte, 1981 , vol. 114, # 3 p. 1099 - 1110 |
|
~%
2(1H)-Pyrimidin... CAS#:21038-75-5 |
| Literature: Schmidt, Arthur H.; Russ, Manuel Chemische Berichte, 1981 , vol. 114, # 3 p. 1099 - 1110 |
|
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: Primary Screen Inhibitors of CD40 Signaling in BL2 Cells Measured in Cell-Based Syste...
Source: Broad Institute
Target: N/A
External Id: 7124-01_Inhibitor_SinglePoint_HTS_Activity
|
| hms3085m23 |