Pyridine,2-[2-(1-piperidinyl)ethyl] structure
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Common Name | Pyridine,2-[2-(1-piperidinyl)ethyl] | ||
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| CAS Number | 5452-83-5 | Molecular Weight | 190.28500 | |
| Density | 1.006g/cm3 | Boiling Point | 272.3ºC at 760mmHg | |
| Molecular Formula | C12H18N2 | Melting Point | N/A | |
| MSDS | N/A | Flash Point | 123.1ºC | |
| Name | 2-(2-piperidin-1-ylethyl)pyridine |
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| Synonym | More Synonyms |
| Density | 1.006g/cm3 |
|---|---|
| Boiling Point | 272.3ºC at 760mmHg |
| Molecular Formula | C12H18N2 |
| Molecular Weight | 190.28500 |
| Flash Point | 123.1ºC |
| Exact Mass | 190.14700 |
| PSA | 16.13000 |
| LogP | 2.04790 |
| Index of Refraction | 1.531 |
| InChIKey | ZOXWZYTVCGKPOX-UHFFFAOYSA-N |
| SMILES | c1ccc(CCN2CCCCC2)nc1 |
CHEMICAL IDENTIFICATION
HEALTH HAZARD DATAACUTE TOXICITY DATA
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| Hazard Codes | Xi |
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| HS Code | 2933990090 |
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Pyridine,2-[2-(... CAS#:5452-83-5
Learn More
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| Literature: Selimov, F. A.; Khafizov, V. R.; Dzhemilev, U. M. Chemistry of Heterocyclic Compounds (New York, NY, United States), 1984 , vol. 20, # 3 p. 290 - 295 Khimiya Geterotsiklicheskikh Soedinenii, 1984 , vol. 20, # 3 p. 360 - 365 |
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Pyridine,2-[2-(... CAS#:5452-83-5 |
| Literature: Profft CHEMTECH, 1955 , vol. 7, p. 511,517 |
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~%
Pyridine,2-[2-(... CAS#:5452-83-5 |
| Literature: Profft CHEMTECH, 1955 , vol. 7, p. 511,517 |
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~79%
Pyridine,2-[2-(... CAS#:5452-83-5 |
| Literature: Heller, Barbara; Sundermann, Bernd; Buschmann, Helmut; Drexler, Hans-Joachim; You, Jingsong; Holzgrabe, Ulrike; Heller, Eberhard; Oehme, Guenther Journal of Organic Chemistry, 2002 , vol. 67, # 13 p. 4414 - 4422 |
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~%
Pyridine,2-[2-(... CAS#:5452-83-5 |
| Literature: Profft CHEMTECH, 1955 , vol. 7, p. 511,517 |
|
~%
Pyridine,2-[2-(... CAS#:5452-83-5 |
| Literature: Beller, Matthias; Trauthwein, Harald; Eichberger, Martin; Breindl, Claudia; Mueller, Thomas E. European Journal of Inorganic Chemistry, 1999 , # 7 p. 1121 - 1132 |
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~%
Pyridine,2-[2-(... CAS#:5452-83-5 |
| Literature: Beller, Matthias; Trauthwein, Harald; Eichberger, Martin; Breindl, Claudia; Mueller, Thomas E. European Journal of Inorganic Chemistry, 1999 , # 7 p. 1121 - 1132 |
| 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: 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
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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: 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: 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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| einecs 226-696-8 |