2-Pyrimidinamine,5-methyl-4-phenyl
Modify Date: 2026-07-10 20:04:49
2-Pyrimidinamine,5-methyl-4-phenyl structure
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Common Name | 2-Pyrimidinamine,5-methyl-4-phenyl | ||
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| CAS Number | 61541-77-3 | Molecular Weight | 185.22500 | |
| Density | 1.159 g/cm3 | Boiling Point | 386.2ºC at 760 mmHg | |
| Molecular Formula | C11H11N3 | Melting Point | N/A | |
| MSDS | N/A | Flash Point | 215.7ºC | |
| Name | 5-methyl-4-phenylpyrimidin-2-amine |
|---|---|
| Synonym | More Synonyms |
| Density | 1.159 g/cm3 |
|---|---|
| Boiling Point | 386.2ºC at 760 mmHg |
| Molecular Formula | C11H11N3 |
| Molecular Weight | 185.22500 |
| Flash Point | 215.7ºC |
| Exact Mass | 185.09500 |
| PSA | 51.80000 |
| LogP | 2.61540 |
| Index of Refraction | 1.619 |
| InChIKey | JVMSDEJRNSSPMM-UHFFFAOYSA-N |
| SMILES | Cc1cnc(N)nc1-c1ccccc1 |
| HS Code | 2933599090 |
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| HS Code | 2933599090 |
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| Summary | 2933599090. other compounds containing a pyrimidine ring (whether or not hydrogenated) or piperazine ring in the structure. VAT:17.0%. Tax rebate rate:13.0%. . MFN tariff:6.5%. General tariff:20.0% |
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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
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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: 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: 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
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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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|
Name: Fluorescence polarization-based biochemical high throughput primary assay to identify...
Source: The Scripps Research Institute Molecular Screening Center
Target: abhydrolase domain-containing protein 4 isoform 1 [Mus musculus]
External Id: ABHD4_INH_FP_1536_1X%INH PRUN
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| 2-Amino-4-phenyl-5-methyl-pyrimidin |
| 2-Pyrimidinamine,5-methyl-4-phenyl |
| 5-methyl-4-phenyl-pyrimidin-2-ylamine |
| 5-methyl-4-phenylpyrimidine-2-amine |
| 2-Amino-5-methyl-4-phenyl-pyrimidin |