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(2-氨基-3-噻吩)(4-氯苯基)甲酮

更新时间:2025-09-14 18:34:49

(2-氨基-3-噻吩)(4-氯苯基)甲酮结构式
(2-氨基-3-噻吩)(4-氯苯基)甲酮结构式
委托求购
常用名 (2-氨基-3-噻吩)(4-氯苯基)甲酮 英文名 (2-AMINO-1-PHENYLETHYL)DIMETHYLAMINE
CAS号 55865-51-5 分子量 237.70500
密度 N/A 沸点 N/A
分子式 C11H8ClNOS 熔点 N/A
MSDS N/A 闪点 N/A

 (2-氨基-3-噻吩)(4-氯苯基)甲酮名称

中文名 (2-氨基-3-噻吩)(4-氯苯基)甲酮
英文名 (2-aminothiophen-3-yl)-(4-chlorophenyl)methanone

 (2-氨基-3-噻吩)(4-氯苯基)甲酮物理化学性质

分子式 C11H8ClNOS
分子量 237.70500
精确质量 237.00200
PSA 71.33000
LogP 3.79590
InChIKey HFLMHMGIVXQGIB-UHFFFAOYSA-N
SMILES Nc1sccc1C(=O)c1ccc(Cl)cc1

 (2-氨基-3-噻吩)(4-氯苯基)甲酮安全信息

海关编码 2934999090

 (2-氨基-3-噻吩)(4-氯苯基)甲酮合成线路

~87%

(2-氨基-3-噻吩)(4-氯苯基)甲酮结构式

(2-氨基-3-噻吩)(4-氯苯基)甲酮

55865-51-5

文献:Ma, Lichao; Yuan, Liwei; Xu, Changzhu; Li, Guowei; Tao, Minli; Zhang, Wenqin Synthesis (Germany), 2013 , vol. 45, # 1 art. no. SS-2012-H0716-OP, p. 45 - 52

~43%

(2-氨基-3-噻吩)(4-氯苯基)甲酮结构式

(2-氨基-3-噻吩)(4-氯苯基)甲酮

55865-51-5

文献:Baraldi, Pier Giovanni; Zaid, Abdel Naser; Lampronti, Ilaria; Fruttarolo, Francesca; Pavani, Maria Giovanna; Tabrizi, Mojgan Aghazadhe; Shryock, John C.; Leung, Edward; Romagnoli, Romeo Bioorganic and Medicinal Chemistry Letters, 2000 , vol. 10, # 17 p. 1953 - 1957

~%

(2-氨基-3-噻吩)(4-氯苯基)甲酮结构式

(2-氨基-3-噻吩)(4-氯苯基)甲酮

55865-51-5

文献:Baraldi, Pier Giovanni; Zaid, Abdel Naser; Lampronti, Ilaria; Fruttarolo, Francesca; Pavani, Maria Giovanna; Tabrizi, Mojgan Aghazadhe; Shryock, John C.; Leung, Edward; Romagnoli, Romeo Bioorganic and Medicinal Chemistry Letters, 2000 , vol. 10, # 17 p. 1953 - 1957

~%

(2-氨基-3-噻吩)(4-氯苯基)甲酮结构式

(2-氨基-3-噻吩)(4-氯苯基)甲酮

55865-51-5

文献:Ma, Lichao; Yuan, Liwei; Xu, Changzhu; Li, Guowei; Tao, Minli; Zhang, Wenqin Synthesis (Germany), 2013 , vol. 45, # 1 art. no. SS-2012-H0716-OP, p. 45 - 52

~%

(2-氨基-3-噻吩)(4-氯苯基)甲酮结构式

(2-氨基-3-噻吩)(4-氯苯基)甲酮

55865-51-5

文献:Ma, Lichao; Yuan, Liwei; Xu, Changzhu; Li, Guowei; Tao, Minli; Zhang, Wenqin Synthesis (Germany), 2013 , vol. 45, # 1 art. no. SS-2012-H0716-OP, p. 45 - 52

 (2-氨基-3-噻吩)(4-氯苯基)甲酮上下游产品

(2-氨基-3-噻吩)(4-氯苯基)甲酮上游产品  6

(2-氨基-3-噻吩)(4-氯苯基)甲酮下游产品  0

 (2-氨基-3-噻吩)(4-氯苯基)甲酮海关

海关编码 2934999090
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%

 (2-氨基-3-噻吩)(4-氯苯基)甲酮靶点实验

查看更多实验

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
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
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
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
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.
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
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
实验名称:Allosteric enhancement of human adenosine A1 receptor expressed in CHO FlpIn cells as...
来源:ChEMBL
靶标:Adenosine receptor A1
External Id:CHEMBL1247044
实验名称:Allosteric enhancement of human adenosine A1 receptor expressed in CHO FlpIn cells as...
来源:ChEMBL
靶标:Adenosine receptor A1
External Id:CHEMBL1247043
实验名称:Allosteric enhancement of human adenosine A1 receptor expressed in CHO FlpIn cells as...
来源:ChEMBL
靶标:Adenosine receptor A1
External Id:CHEMBL1247042
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