6-Chloro-3-hydroxypyridazine
Modify Date: 2025-08-25 18:18:19
6-Chloro-3-hydroxypyridazine structure
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Common Name | 6-Chloro-3-hydroxypyridazine | ||
|---|---|---|---|---|
| CAS Number | 19064-67-6 | Molecular Weight | 130.532 | |
| Density | 1.5±0.1 g/cm3 | Boiling Point | 350.3±22.0 °C at 760 mmHg | |
| Molecular Formula | C4H3ClN2O | Melting Point | 140.0 to 144.0 °C | |
| MSDS | N/A | Flash Point | 165.6±22.3 °C | |
| Name | 6-Chloropyridazin-3-ol |
|---|---|
| Synonym | More Synonyms |
| Density | 1.5±0.1 g/cm3 |
|---|---|
| Boiling Point | 350.3±22.0 °C at 760 mmHg |
| Melting Point | 140.0 to 144.0 °C |
| Molecular Formula | C4H3ClN2O |
| Molecular Weight | 130.532 |
| Flash Point | 165.6±22.3 °C |
| Exact Mass | 129.993393 |
| PSA | 45.75000 |
| LogP | 0.81 |
| Vapour Pressure | 0.0±0.8 mmHg at 25°C |
| Index of Refraction | 1.593 |
| InChIKey | YICPBKWYZXFJNB-UHFFFAOYSA-N |
| SMILES | O=c1ccc(Cl)n[nH]1 |
| Storage condition | Room temperature. |
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~95%
6-Chloro-3-hydr... CAS#:19064-67-6 |
| Literature: Johnston, Karen A.; Allcock, Robert W.; Jiang, Zhong; Collier, Ian D.; Blakli, Haakon; Rosair, Georgina M.; Bailey, Patrick D.; Morgan, Keith M.; Kohno, Yasushi; Adams, David R. Organic and Biomolecular Chemistry, 2008 , vol. 6, # 1 p. 175 - 186 |
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6-Chloro-3-hydr... CAS#:19064-67-6 |
| Literature: Journal of Organic Chemistry, , vol. 24, p. 811 |
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6-Chloro-3-hydr... CAS#:19064-67-6 |
| Literature: Journal of the Chemical Society, Perkin Transactions 2: Physical Organic Chemistry (1972-1999), , p. 1255 - 1258 |
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6-Chloro-3-hydr... CAS#:19064-67-6 |
| Literature: Pharmaceutical Bulletin, , vol. 5, p. 376,377 Pharmaceutical Bulletin, , vol. 6, p. 641 |
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6-Chloro-3-hydr... CAS#:19064-67-6 |
| Literature: Arkiv foer Kemi, , vol. 14, p. 419,421 |
| Precursor 5 | |
|---|---|
| DownStream 6 | |
CAS#:10071-38-2
CAS#:1698-57-3
CAS#:71173-10-9
CAS#:89581-61-3
CAS#:90932-14-2| 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: Primary cell-based high-throughput screening assay for identification of compounds th...
Source: Johns Hopkins Ion Channel Center
Target: regulator of G-protein signaling 4 isoform 2 [Homo sapiens]
External Id: JHICC_RGS_Act_HTS
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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
|
|
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: uHTS identification of small molecule activators of the adaptive arm of the Unfolded ...
Source: Burnham Center for Chemical Genomics
Target: N/A
External Id: BCCG-A405-UPR-XBP1-PrimaryAgonist-Assay
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|
Name: Antibacterial activity against Klebsiella pneumoniae MDR ATCC 70063 (CO-ADD:GN_003); ...
Source: ChEMBL
Target: Klebsiella pneumoniae
External Id: CHEMBL4296186
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|
Name: High throughput fluorescence intensity-based biochemical assay to screen for small mo...
Source: University of Pittsburgh Molecular Library Screening Center
Target: furin (paired basic amino acid cleaving enzyme), isoform CRA_a [Homo sapiens]
External Id: MH080376 Biochemical HTS for Inhibitors of the Proprotein Convertase Furin.
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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: Identifying Sarm1 TIR NADase inhibitors through high throughput HPLC assay
Source: 24386
Target: N/A
External Id: Sarm1 TIR NADase inhibitors
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| 6-Chloro-3(2H)-pyridazinone |
| 6-Chloropyridazin-3(2H)-one |
| 6-Chloropyridazin-3-ol |
| 3-Chloro-6-pyridazone |
| 6-Chloro-3-pyridazinol |
| 3-chloro-1H-pyridazin-6-one |
| 6-chloro-2H-pyridazin-3-one |
| 6-Chloropyridazine-3-ol |
| 6-Chloro-3-hydroxypyridazine |
| 6-chloro-3-pyridazinone |
| 6-Chloro-3-hydroxypyridaz... |
| 3-Hydroxy-6-chloropyridazine |
| 3-Chloro-6-hydroxypyridazine |
| 3-chloro-1,6-dihydro-6-oxo-pyridazine |