Picolinaldehyde, 2-quinolylhydrazone structure
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Common Name | Picolinaldehyde, 2-quinolylhydrazone | ||
|---|---|---|---|---|
| CAS Number | 7385-99-1 | Molecular Weight | 248.28300 | |
| Density | 1.19g/cm3 | Boiling Point | 459.8ºC at 760 mmHg | |
| Molecular Formula | C15H12N4 | Melting Point | 203-206ºC | |
| MSDS | N/A | Flash Point | 231.9ºC | |
| Name | Pyridine-2-Carboxaldehyde 2-Quinolylhydrazone |
|---|---|
| Synonym | More Synonyms |
| Density | 1.19g/cm3 |
|---|---|
| Boiling Point | 459.8ºC at 760 mmHg |
| Melting Point | 203-206ºC |
| Molecular Formula | C15H12N4 |
| Molecular Weight | 248.28300 |
| Flash Point | 231.9ºC |
| Exact Mass | 248.10600 |
| PSA | 50.17000 |
| LogP | 3.14880 |
| Index of Refraction | 1.656 |
| InChIKey | RQKUHYQNHJJIFO-UHFFFAOYSA-N |
| SMILES | C(=NNc1ccc2ccccc2n1)c1ccccn1 |
| Safety Phrases | S22-S24/25 |
|---|---|
| HS Code | 2933990090 |
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~%
Picolinaldehyde... CAS#:7385-99-1 |
| Literature: The Procter and Gamble Company Patent: US2003/92716 A1, 2003 ; |
| HS Code | 2933990090 |
|---|---|
| Summary | 2933990090. heterocyclic compounds with nitrogen hetero-atom(s) only. 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: Counterscreen for inhibitors of the Steroid Receptor Coactivator 1 (SRC1; NCOA1): Lum...
Source: The Scripps Research Institute Molecular Screening Center
Target: transactivating tegument protein VP16 [Human herpesvirus 1]
External Id: VP16_INH_LUMI_1536_3X%INH CSRUN for SRC1
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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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| MFCD00014660 |
| EINECS 230-967-6 |
| Pyridine-2-carboxaldehyde 2-quinolylhydrazone, 98+% |