2(3H)-Thiazolone,4-(4-chlorophenyl)
Modify Date: 2025-08-25 14:38:15
2(3H)-Thiazolone,4-(4-chlorophenyl) structure
|
Common Name | 2(3H)-Thiazolone,4-(4-chlorophenyl) | ||
|---|---|---|---|---|
| CAS Number | 2103-98-2 | Molecular Weight | 211.66800 | |
| Density | 1.428g/cm3 | Boiling Point | 410.2ºC at 760mmHg | |
| Molecular Formula | C9H6ClNOS | Melting Point | 222-226ºC | |
| MSDS | Chinese USA | Flash Point | 201.9ºC | |
| Symbol |
GHS05, GHS06 |
Signal Word | Danger | |
| Name | 4-(4-chlorophenyl)-3H-1,3-thiazol-2-one |
|---|---|
| Synonym | More Synonyms |
| Density | 1.428g/cm3 |
|---|---|
| Boiling Point | 410.2ºC at 760mmHg |
| Melting Point | 222-226ºC |
| Molecular Formula | C9H6ClNOS |
| Molecular Weight | 211.66800 |
| Flash Point | 201.9ºC |
| Exact Mass | 210.98600 |
| PSA | 61.10000 |
| LogP | 2.75680 |
| Vapour Pressure | 2.58E-07mmHg at 25°C |
| Index of Refraction | 1.655 |
| InChIKey | XODFWCAVOQHJFC-UHFFFAOYSA-N |
| SMILES | O=c1[nH]c(-c2ccc(Cl)cc2)cs1 |
| Symbol |
GHS05, GHS06 |
|---|---|
| Signal Word | Danger |
| Hazard Statements | H301-H315-H318-H335 |
| Precautionary Statements | P261-P280-P301 + P310-P305 + P351 + P338 |
| Personal Protective Equipment | dust mask type N95 (US);Eyeshields;Faceshields;Gloves |
| Hazard Codes | Xn: Harmful; |
| Risk Phrases | R22 |
| Safety Phrases | 26-36/37/39 |
| RIDADR | UN 2811 6.1/PG 3 |
| HS Code | 2934100090 |
|
~91%
2(3H)-Thiazolon... CAS#:2103-98-2 |
| Literature: Takeda Chemical Industries, Ltd.; Kusaka, Masami Patent: EP1348706 A1, 2003 ; Location in patent: Page/Page column 40-41 ; |
|
~66%
2(3H)-Thiazolon... CAS#:2103-98-2 |
| Literature: Sanemitsu; Kawamura; Tanabe Journal of Organic Chemistry, 1992 , vol. 57, # 3 p. 1053 - 1056 |
|
~%
2(3H)-Thiazolon... CAS#:2103-98-2 |
| Literature: Journal of the American Chemical Society, , vol. 80, p. 5198 |
|
~%
2(3H)-Thiazolon... CAS#:2103-98-2 |
| Literature: Synthetic Communications, , vol. 23, # 10 p. 1455 - 1462 |
| HS Code | 2934100090 |
|---|---|
| Summary | 2934100090 other compounds containing an unfused thiazole 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
|
|
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
|
|
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
|
|
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
|
|
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
|
|
Name: Fluorescence-based cell-based primary high throughput screening assay to identify pos...
Source: The Scripps Research Institute Molecular Screening Center
Target: muscarinic acetylcholine receptor M1 [Homo sapiens]
External Id: CHRM1_PAM_FLUO8_1536_1X%ACT PRUN
|
|
Name: Fluorescence polarization-based biochemical high throughput primary assay to identify...
Source: The Scripps Research Institute Molecular Screening Center
Target: RecName: Full=Sialate O-acetylesterase; AltName: Full=H-Lse; AltName: Full=Sialic acid-specific 9-O-acetylesterase; Flags: Precursor [Homo sapiens]
External Id: SIAE_INH_FP_1536_1X%INH PRUN
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| 4-(4-chlorophenyl)-2-oxo-1,3-thiazole |
| 4-p-Chlorphenyl-4-thiazolin-2-on |
| (4-chlorophenyl)-2(3H)-thiazolone |
| 4-(4-Chlor-phenyl)-3H-thiazol-2-on |
| 4-(4-chloro-phenyl)-3H-thiazol-2-one |
| 4-(4-CHLOROPHENYL)-2-HYDROXYTHIAZOLE |
| 2-thiazolol,4-(4-chlorophenyl) |
| 4-(4-chlorophenyl)-2-oxo-thiazole |