2,6-bis(2-furylmethylidene)cyclohexan-1-one
Modify Date: 2025-08-25 20:31:24
2,6-bis(2-furylmethylidene)cyclohexan-1-one structure
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Common Name | 2,6-bis(2-furylmethylidene)cyclohexan-1-one | ||
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| CAS Number | 893-00-5 | Molecular Weight | 254.28100 | |
| Density | 1.245g/cm3 | Boiling Point | 422.9ºC at 760 mmHg | |
| Molecular Formula | C16H14O3 | Melting Point | N/A | |
| MSDS | N/A | Flash Point | 204.5ºC | |
| Name | 2,6-bis(furan-2-ylmethylidene)cyclohexan-1-one |
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| Synonym | More Synonyms |
| Density | 1.245g/cm3 |
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| Boiling Point | 422.9ºC at 760 mmHg |
| Molecular Formula | C16H14O3 |
| Molecular Weight | 254.28100 |
| Flash Point | 204.5ºC |
| Exact Mass | 254.09400 |
| PSA | 43.35000 |
| LogP | 4.09260 |
| Index of Refraction | 1.641 |
| InChIKey | KWHQMDCQGGHVJP-DCIPZJNNSA-N |
| SMILES | O=C1C(=Cc2ccco2)CCCC1=Cc1ccco1 |
| HS Code | 2932190090 |
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| HS Code | 2932190090 |
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| Summary | 2932190090 other compounds containing an unfused furan ring (whether or not hydrogenated) in the structure VAT:17.0% Tax rebate rate:9.0% Supervision conditions:none 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
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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: Single Concentration Validation of Csn-Mediated Deneddylation of Cullin-Ring Ligase U...
Source: Burnham Center for Chemical Genomics
Target: COP9 signalosome complex subunit 5 [Homo sapiens]
External Id: SBCCG-A995-CSN5-CP-Assay
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Name: Single concentration validation of Csn-Mediated Deneddylation of Cullin-Ring Ligase H...
Source: Burnham Center for Chemical Genomics
Target: 72 kDa type IV collagenase isoform a preproprotein [Homo sapiens]
External Id: SBCCG-A996-CSN5-MMP2-CP-Assay
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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: 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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| 2,6-difurfurylidenecyclohexanone |