2-(4-甲基苯基)-1,3-噻唑烷结构式
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常用名 | 2-(4-甲基苯基)-1,3-噻唑烷 | 英文名 | 2-(DIFLUOROMETHYL)-1-FLUOROBENZENE |
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| CAS号 | 67086-82-2 | 分子量 | 179.28200 | |
| 密度 | 1.088g/cm3 | 沸点 | 318.5ºC at 760 mmHg | |
| 分子式 | C10H13NS | 熔点 | N/A | |
| MSDS | N/A | 闪点 | 146.4ºC |
| 中文名 | 2-(4-甲基苯基)-1,3-噻唑烷 |
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| 英文名 | 2-(4-methylphenyl)-1,3-thiazolidine |
| 英文别名 | 更多 |
| 密度 | 1.088g/cm3 |
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| 沸点 | 318.5ºC at 760 mmHg |
| 分子式 | C10H13NS |
| 分子量 | 179.28200 |
| 闪点 | 146.4ºC |
| 精确质量 | 179.07700 |
| PSA | 37.33000 |
| LogP | 2.65880 |
| InChIKey | NLKGQUAQKCOAHV-UHFFFAOYSA-N |
| SMILES | Cc1ccc(C2NCCS2)cc1 |
| 折射率 | 1.577 |
| 海关编码 | 2934999090 |
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2-(4-甲基苯基)-1,3-噻唑烷 67086-82-2 |
| 文献:Richter Gedeon Vegyeszeti Gyar RT Patent: US4616025 A1, 1986 ; |
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2-(4-甲基苯基)-1,3-噻唑烷 67086-82-2 |
| 文献:Nate; Sekine; Honma; Nakai; Wada; Takeda; Yabana; Nagao Chemical and pharmaceutical bulletin, 1987 , vol. 35, # 5 p. 1953 - 1968 |
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2-(4-甲基苯基)-1,3-噻唑烷 67086-82-2 |
| 文献:Robbe; Fernandez; Dubief; et al. European Journal of Medicinal Chemistry, 1982 , vol. 17, # 3 p. 235 - 243 |
| 2-(4-甲基苯基)-1,3-噻唑烷上游产品 3 | |
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| 2-(4-甲基苯基)-1,3-噻唑烷下游产品 0 | |
| 海关编码 | 2934999090 |
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| 中文概述 | 2934999090. 其他杂环化合物. 增值税率:17.0%. 退税率:13.0%. 监管条件:无. 最惠国关税:6.5%. 普通关税:20.0% |
| 申报要素 | 品名, 成分含量, 用途 |
| 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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实验名称:Primary cell-based high-throughput screening assay for identification of compounds th...
来源:Johns Hopkins Ion Channel Center
靶标:regulator of G-protein signaling 4 isoform 2 [Homo sapiens]
External Id:JHICC_RGS_Act_HTS
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实验名称:Luminescence-based cell-based primary high throughput screening assay to identify ago...
来源:The Scripps Research Institute Molecular Screening Center
靶标:mu-type opioid receptor isoform MOR-1 [Homo sapiens]
External Id:OPRM1-OPRD1_AG_LUMI_1536_1X%ACT PRUN
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实验名称:QFRET-based biochemical primary high throughput screening assay to identify exosite i...
来源:The Scripps Research Institute Molecular Screening Center
靶标:disintegrin and metalloproteinase domain-containing protein 17 preproprotein [Homo sapiens]
External Id:ADAM17_INH_QFRET_1536_1X%INH PRUN
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实验名称:Fluorescence-based cell-based primary high throughput screening assay to identify ago...
来源:The Scripps Research Institute Molecular Screening Center
靶标:muscarinic acetylcholine receptor M1 [Homo sapiens]
External Id:CHRM1_AG_FLUO8_1536_1X%ACT PRUN
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实验名称:uHTS identification of small molecule activators of the adaptive arm of the Unfolded ...
来源:Burnham Center for Chemical Genomics
靶标:N/A
External Id:BCCG-A405-UPR-XBP1-PrimaryAgonist-Assay
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实验名称:A screen for compounds that inhibit the activity of LtaS in Staphylococcus aureus
来源:ICCB-Longwood/NSRB Screening Facility, Harvard Medical School
External Id:HMS979
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实验名称:High throughput fluorescence intensity-based biochemical assay to screen for small mo...
来源:University of Pittsburgh Molecular Library Screening Center
靶标: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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实验名称:Fluorescence polarization to screen for inhibitor that competite the binding of FadD2...
来源:Broad Institute
靶标:FATTY-ACID-CoA LIGASE FADD28 (FATTY-ACID-CoA SYNTHETASE)
External Id:2147-01_Inhibitor_SinglePoint_HTS_Activity
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实验名称:Bursicon-induced LGR2 mediated cAMP production in LGR-2/CRE6x-Luciferase co-transfect...
来源:Broad Institute
靶标: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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实验名称:Fluorescence-based cell-based primary high throughput screening assay to identify pos...
来源:The Scripps Research Institute Molecular Screening Center
靶标:muscarinic acetylcholine receptor M1 [Homo sapiens]
External Id:CHRM1_PAM_FLUO8_1536_1X%ACT PRUN
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| 2-(4-methylphenyl)-thiazolidine |
| 2-(p-Methylphenyl)thiazolidine |
| 2-(4-methylphenyl)-1,3-thiazolane |
| methylphenylthiazolane |
| Thiazolidine,2-(p-tolyl) |
| 2-(p-Tolyl)thiazolidine |