ethyl N-(thiadiazol-4-yl)carbamate
Modify Date: 2025-10-07 16:23:19
ethyl N-(thiadiazol-4-yl)carbamate structure
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Common Name | ethyl N-(thiadiazol-4-yl)carbamate | ||
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| CAS Number | 4100-29-2 | Molecular Weight | 173.19300 | |
| Density | 1.427g/cm3 | Boiling Point | N/A | |
| Molecular Formula | C5H7N3O2S | Melting Point | N/A | |
| MSDS | N/A | Flash Point | N/A | |
| Name | ethyl N-(thiadiazol-4-yl)carbamate |
|---|---|
| Synonym | More Synonyms |
| Density | 1.427g/cm3 |
|---|---|
| Molecular Formula | C5H7N3O2S |
| Molecular Weight | 173.19300 |
| Exact Mass | 173.02600 |
| PSA | 92.35000 |
| LogP | 1.17950 |
| Index of Refraction | 1.599 |
| InChIKey | CBFRLNIFUGURTG-UHFFFAOYSA-N |
| SMILES | CCOC(=O)Nc1csnn1 |
| HS Code | 2934999090 |
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~%
ethyl N-(thiadi... CAS#:4100-29-2 |
| Literature: Looker,J.H.; Wilson,L.W. Journal of Heterocyclic Chemistry, 1965 , vol. 2, p. 348 - 354 |
|
~%
ethyl N-(thiadi... CAS#:4100-29-2 |
| Literature: Pain,D.L.; Slack,R. Journal of the Chemical Society, 1965 , p. 5166 - 5176 |
| Precursor 3 | |
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| DownStream 0 | |
| HS Code | 2934999090 |
|---|---|
| Summary | 2934999090. other heterocyclic compounds. 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: 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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| ethyl 1,2,3-thiadiazol-4-ylcarbamate |
| 4-Ethoxycarbonylamino-1.2.3-thiadiazole |
| 4-Aethoxycarbonylamino-1.2.3-thiadiazol |
| HMS2884C21 |
| 4-Aethoxyformamino-1.2.3-thiadiazol |