2-苯基-4-氯-6-甲基嘧啶结构式
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常用名 | 2-苯基-4-氯-6-甲基嘧啶 | 英文名 | 4-chloro-6-methyl-2-phenylpyrimidine |
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| CAS号 | 29509-92-0 | 分子量 | 204.65600 | |
| 密度 | 1.208g/cm3 | 沸点 | 232ºC at 760 mmHg | |
| 分子式 | C11H9ClN2 | 熔点 | N/A | |
| MSDS | N/A | 闪点 | 116.4ºC |
| 中文名 | 4-氯-6-甲基-2-苯基嘧啶 |
|---|---|
| 英文名 | 4-chloro-6-methyl-2-phenylpyrimidine |
| 英文别名 | 更多 |
| 密度 | 1.208g/cm3 |
|---|---|
| 沸点 | 232ºC at 760 mmHg |
| 分子式 | C11H9ClN2 |
| 分子量 | 204.65600 |
| 闪点 | 116.4ºC |
| 精确质量 | 204.04500 |
| PSA | 25.78000 |
| LogP | 3.10540 |
| InChIKey | MOLLLUIWZOISLC-UHFFFAOYSA-N |
| SMILES | Cc1cc(Cl)nc(-c2ccccc2)n1 |
| 蒸汽压 | 0.0918mmHg at 25°C |
| 折射率 | 1.584 |
| 储存条件 | 2-8°C |
| 危害码 (欧洲) | Xi: Irritant; |
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| 海关编码 | 2933599090 |
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2-苯基-4-氯-6-甲基嘧啶 29509-92-0 |
| 文献:Bioorganic and Medicinal Chemistry, , vol. 20, # 7 p. 2369 - 2375 |
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~93%
2-苯基-4-氯-6-甲基嘧啶 29509-92-0 |
| 文献:Brown; Cowden; Lan; Mori Australian Journal of Chemistry, 1984 , vol. 37, # 1 p. 155 - 163 |
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2-苯基-4-氯-6-甲基嘧啶 29509-92-0 |
| 文献:Australian Journal of Chemistry, , vol. 37, # 1 p. 155 - 163 |
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2-苯基-4-氯-6-甲基嘧啶 29509-92-0 |
| 文献:Bioorganic and Medicinal Chemistry, , vol. 20, # 7 p. 2369 - 2375 |
|
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2-苯基-4-氯-6-甲基嘧啶 29509-92-0 |
| 文献:Journal of Heterocyclic Chemistry, , vol. 34, # 5 p. 1639 - 1641 |
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2-苯基-4-氯-6-甲基嘧啶 29509-92-0 |
| 文献:Chemische Berichte, , vol. 17, p. 2520 Chemische Berichte, , vol. 18, p. 762 |
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2-苯基-4-氯-6-甲基嘧啶 29509-92-0 |
| 文献:Chemische Berichte, , vol. 35, p. 1577 |
| 2-苯基-4-氯-6-甲基嘧啶上游产品 8 | |
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| 2-苯基-4-氯-6-甲基嘧啶下游产品 10 | |
| 海关编码 | 2933599090 |
|---|---|
| 中文概述 | 2933599090. 其他结构上有嘧啶环的化合物(包括其他结构上有哌嗪环的化合物. 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, 乌洛托品请注明外观, 6-己内酰胺请注明外观, 签约日期 |
| Summary | 2933599090. other compounds containing a pyrimidine ring (whether or not hydrogenated) or piperazine ring in the structure. 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:Primary Screen Inhibitors of CD40 Signaling in BL2 Cells Measured in Cell-Based Syste...
来源:Broad Institute
靶标:N/A
External Id:7124-01_Inhibitor_SinglePoint_HTS_Activity
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| Pyrimidine,4-chloro-6-methyl-2-phenyl |
| 4-Chlor-6-methyl-2-phenyl-pyrimidin |
| 6-chloro-4-methyl-2-phenylpyrimidine |
| 4-chloro-6-methyl-2-phenyl-pyrimidine |