Benzamide,N-[(4-chlorophenyl)sulfonyl]
Modify Date: 2025-08-25 19:05:37
![Benzamide,N-[(4-chlorophenyl)sulfonyl] Structure](https://image.chemsrc.com/caspic/059/14067-98-2.png)
Benzamide,N-[(4-chlorophenyl)sulfonyl] structure
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Common Name | Benzamide,N-[(4-chlorophenyl)sulfonyl] | ||
|---|---|---|---|---|
| CAS Number | 14067-98-2 | Molecular Weight | 295.74100 | |
| Density | 1.399g/cm3 | Boiling Point | N/A | |
| Molecular Formula | C13H10ClNO3S | Melting Point | N/A | |
| MSDS | N/A | Flash Point | N/A | |
| Name | N-(4-chlorophenyl)sulfonylbenzamide |
|---|---|
| Synonym | More Synonyms |
| Density | 1.399g/cm3 |
|---|---|
| Molecular Formula | C13H10ClNO3S |
| Molecular Weight | 295.74100 |
| Exact Mass | 295.00700 |
| PSA | 71.62000 |
| LogP | 3.93040 |
| Index of Refraction | 1.612 |
| InChIKey | BUVKGFNBMCHZJN-UHFFFAOYSA-N |
| SMILES | O=C(NS(=O)(=O)c1ccc(Cl)cc1)c1ccccc1 |
| HS Code | 2924299090 |
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~89%
Benzamide,N-[(4... CAS#:14067-98-2 |
| Literature: Wang, Ying; Sarris, Kathy; Sauer, Daryl R.; Djuric, Stevan W. Tetrahedron Letters, 2007 , vol. 48, # 30 p. 5181 - 5184 |
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~91%
Benzamide,N-[(4... CAS#:14067-98-2 |
| Literature: Yates, Matthew H.; Kallman, Neil J.; Ley, Christopher P.; Wei, Jeffrey N. Organic Process Research and Development, 2009 , vol. 13, # 2 p. 255 - 262 |
|
~78%
Benzamide,N-[(4... CAS#:14067-98-2 |
| Literature: Singh, Devendrapratap U.; Singh, Pankajkumar R.; Samant, Shriniwas D. Tetrahedron Letters, 2004 , vol. 45, # 24 p. 4805 - 4807 |
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~16%
Benzamide,N-[(4... CAS#:14067-98-2 |
| Literature: Ludwig, Miroslav; Parik, Patrik; Kulhanek, Jiri Collection of Czechoslovak Chemical Communications, 1995 , vol. 60, # 5 p. 841 - 850 |
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~%
Benzamide,N-[(4... CAS#:14067-98-2 |
| Literature: Kutuk, Halil; Tillett, John G. Phosphorus, Sulfur and Silicon and Related Elements, 2001 , vol. 175, p. 35 - 47 |
| HS Code | 2924299090 |
|---|---|
| Summary | 2924299090. other cyclic amides (including cyclic carbamates) and their derivatives; salts thereof. VAT:17.0%. Tax rebate rate:13.0%. . MFN tariff:6.5%. General tariff:30.0% |
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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
|
|
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
|
|
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: A screen for compounds that inhibit the activity of LtaS in Staphylococcus aureus
Source: ICCB-Longwood/NSRB Screening Facility, Harvard Medical School
External Id: HMS979
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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: 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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| T0400-0165 |
| N-(4-chlorophenylsulfonyl)benzamide |
| Benzoyl-(4-chlor-benzolsulfonyl)-amin |
| N-benzoyl-p-chlorobenzenesulfonamide |
| N-(4-chloro-benzenesulfonyl)-benzamide |
| N-(4-Chlor-benzol-sulfonyl-(1))-benzamid |
| benzoyl-(4-chloro-benzenesulfonyl)-amine |