N-pyridin-4-ylbenzene-1,4-diamine
Modify Date: 2025-09-12 17:26:45
N-pyridin-4-ylbenzene-1,4-diamine structure
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Common Name | N-pyridin-4-ylbenzene-1,4-diamine | ||
|---|---|---|---|---|
| CAS Number | 60172-08-9 | Molecular Weight | 185.22500 | |
| Density | 1.226g/cm3 | Boiling Point | 382.9ºC at 760 mmHg | |
| Molecular Formula | C11H11N3 | Melting Point | N/A | |
| MSDS | N/A | Flash Point | 185.4ºC | |
| Name | 4-N-pyridin-4-ylbenzene-1,4-diamine |
|---|---|
| Synonym | More Synonyms |
| Density | 1.226g/cm3 |
|---|---|
| Boiling Point | 382.9ºC at 760 mmHg |
| Molecular Formula | C11H11N3 |
| Molecular Weight | 185.22500 |
| Flash Point | 185.4ºC |
| Exact Mass | 185.09500 |
| PSA | 50.94000 |
| LogP | 3.06160 |
| Index of Refraction | 1.693 |
| InChIKey | BGFGRYYEROKAHI-UHFFFAOYSA-N |
| SMILES | Nc1ccc(Nc2ccncc2)cc1 |
![N-phenyl-N'-[4]pyridyl-hydrazine structure](https://image.chemsrc.com/caspic/241/72109-70-7.png)
![Benzamide,4-nitro-N-[4-(4-pyridinylamino)phenyl] structure](https://image.chemsrc.com/caspic/361/23552-71-8.png)
CAS#:23552-71-8|
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: 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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Name: High Throughput Screen to Identify Inhibitors Targeting HIV-1 Vif-dependent Degradati...
Source: Southern Research Institute
Target: HIV-1 Vif
External Id: HIV1-VIF_MS
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| N-4-pyridinyl-1,4-benzenediamine |