1,3-dimethylbenzimidazoline-2-thione structure
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Common Name | 1,3-dimethylbenzimidazoline-2-thione | ||
|---|---|---|---|---|
| CAS Number | 3418-46-0 | Molecular Weight | 178.25400 | |
| Density | 1.28g/cm3 | Boiling Point | 270.8ºC at 760mmHg | |
| Molecular Formula | C9H10N2S | Melting Point | N/A | |
| MSDS | N/A | Flash Point | 117.6ºC | |
| Name | 1,3-dimethylbenzimidazole-2-thione |
|---|---|
| Synonym | More Synonyms |
| Density | 1.28g/cm3 |
|---|---|
| Boiling Point | 270.8ºC at 760mmHg |
| Molecular Formula | C9H10N2S |
| Molecular Weight | 178.25400 |
| Flash Point | 117.6ºC |
| Exact Mass | 178.05600 |
| PSA | 41.95000 |
| LogP | 2.24630 |
| Index of Refraction | 1.698 |
| InChIKey | CSYLYUAMXUGIFE-UHFFFAOYSA-N |
| SMILES | Cn1c(=S)n(C)c2ccccc21 |
| HS Code | 2933990090 |
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| Precursor 9 | |
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| DownStream 0 | |
| 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
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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: 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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Name: Flow Cytometric HTS Screen for inhibitors of the ABC transporter ABCB6 for Validation...
Source: NMMLSC
Target: ATP-binding cassette sub-family B member 6, mitochondrial [Homo sapiens]
External Id: UNMCMD_ABCB6_1o_ValidationSet
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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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| 1,3-Dime-bit |
| 1,3-Dihydro-1,3-dimethyl-2H-benzimidazol-2-thion |
| N,N'-Dimethylbenzimidazolin-2-thione |
| HMS2695H10 |
| N,N-dimethylbenzimidazole-2-thione |
| N,N'-Dimethylbenzoimidazole-2-thione |
| 1,3-dimethyl-1,3-dihydro-benzoimidazole-2-thione |
| 2H-Benzimidazole-2-thione,1,3-dihydro-1,3-dimethyl |
| 1,3-dimethyl-1,3-dihydro-3H-benzimidazole-2-thione |