1,2,3-Thiadiazole-4-carbamicacid, benzyl ester (7CI,8CI)
Modify Date: 2026-07-18 17:29:50
1,2,3-Thiadiazole-4-carbamicacid, benzyl ester (7CI,8CI) structure
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Common Name | 1,2,3-Thiadiazole-4-carbamicacid, benzyl ester (7CI,8CI) | ||
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| CAS Number | 4100-28-1 | Molecular Weight | 235.26200 | |
| Density | 1.421g/cm3 | Boiling Point | N/A | |
| Molecular Formula | C10H9N3O2S | Melting Point | N/A | |
| MSDS | N/A | Flash Point | N/A | |
| Name | benzyl N-(thiadiazol-4-yl)carbamate |
|---|---|
| Synonym | More Synonyms |
| Density | 1.421g/cm3 |
|---|---|
| Molecular Formula | C10H9N3O2S |
| Molecular Weight | 235.26200 |
| Exact Mass | 235.04200 |
| PSA | 92.35000 |
| LogP | 2.35980 |
| Index of Refraction | 1.663 |
| InChIKey | JCWFPLYWTWIKBM-UHFFFAOYSA-N |
| SMILES | O=C(Nc1csnn1)OCc1ccccc1 |
| HS Code | 2934999090 |
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1,2,3-Thiadiazo... CAS#:4100-28-1 |
| Literature: Pain,D.L.; Slack,R. Journal of the Chemical Society, 1965 , p. 5166 - 5176 |
| Precursor 2 | |
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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: 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: 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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Name: qHTS for Inhibitors of AMA1-RON; Towards Development of Antimalarial Drug Lead: Prima...
Source: NCGC
Target: apical membrane antigen 1, AMA1 [Plasmodium falciparum 3D7]
External Id: AMA1100
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| 4-Benzyloxycarbonylamino-1.2.3-thiadiazol |
| benzyl 1,2,3-thiadiazol-4-ylcarbamate |
| [1,2,3]thiadiazol-4-yl-carbamic acid benzyl ester |