2,6-dichloro-9-phenyl-purine
Modify Date: 2025-08-23 18:51:11
2,6-dichloro-9-phenyl-purine structure
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Common Name | 2,6-dichloro-9-phenyl-purine | ||
|---|---|---|---|---|
| CAS Number | 6971-26-2 | Molecular Weight | 265.09800 | |
| Density | 1.58g/cm3 | Boiling Point | 406.2ºC at 760 mmHg | |
| Molecular Formula | C11H6Cl2N4 | Melting Point | N/A | |
| MSDS | N/A | Flash Point | 199.5ºC | |
| Name | 2,6-dichloro-9-phenylpurine |
|---|---|
| Synonym | More Synonyms |
| Density | 1.58g/cm3 |
|---|---|
| Boiling Point | 406.2ºC at 760 mmHg |
| Molecular Formula | C11H6Cl2N4 |
| Molecular Weight | 265.09800 |
| Flash Point | 199.5ºC |
| Exact Mass | 263.99700 |
| PSA | 43.60000 |
| LogP | 3.12230 |
| Index of Refraction | 1.743 |
| InChIKey | PUARFAPITOZVIH-UHFFFAOYSA-N |
| SMILES | Clc1nc(Cl)c2ncn(-c3ccccc3)c2n1 |
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2,6-dichloro-9-... CAS#:6971-26-2 |
| Literature: Merrell Dow Pharmaceuticals Inc. Patent: US5064947 A1, 1991 ; US 5064947 A |
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~50%
2,6-dichloro-9-... CAS#:6971-26-2 |
| Literature: Bakkestuen, Anne Kristin; Gundersen, Lise-Lotte Tetrahedron Letters, 2003 , vol. 44, # 16 p. 3359 - 3362 |
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~97%
2,6-dichloro-9-... CAS#:6971-26-2 |
| Literature: Niu, Hong-Ying; Xia, Chao; Qu, Gui-Rong; Zhang, Qian; Jiang, Yi; Mao, Run-Ze; Li, De-Yang; Guo, Hai-Ming Organic and Biomolecular Chemistry, 2011 , vol. 9, # 14 p. 5039 - 5042 |
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2,6-dichloro-9-... CAS#:6971-26-2 |
| Literature: Koppel; Robins Journal of the American Chemical Society, 1958 , vol. 80, p. 2751,2753 |
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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
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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
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|
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
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|
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
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|
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
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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
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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
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|
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
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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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| 2,6-dichloro-9-phenyl-9h-purine |
| HMS3095C20 |
| 2,6-dichloro-1-phenylpurine |
| 2,6-dichloro-9-(4-methylphenyl)-purine |
| 2,6-Dichlor-9-phenyl-9H-purin |