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2-氨基-3-(4-氯苯甲酰基)-4,5-二甲基噻吩

更新时间:2025-09-06 17:11:48

2-氨基-3-(4-氯苯甲酰基)-4,5-二甲基噻吩结构式
2-氨基-3-(4-氯苯甲酰基)-4,5-二甲基噻吩结构式
品牌特惠专场
常用名 2-氨基-3-(4-氯苯甲酰基)-4,5-二甲基噻吩 英文名 (2-amino-4,5-dimethylthiophen-3-yl)(4-chlorophenyl)methanone
CAS号 50508-66-2 分子量 265.75800
密度 1.303±0.06g/ml(Predicted) 沸点 435.4±45.0℃(Predicted)
分子式 C13H12ClNOS 熔点 N/A
MSDS N/A 闪点 N/A

 2-氨基-3-(4-氯苯甲酰基)-4,5-二甲基噻吩名称

中文名 (2-氨基-4,5-二甲基-3-噻吩)(4-氯苯基)甲酮
英文名 (2-amino-4,5-dimethylthiophen-3-yl)-(4-chlorophenyl)methanone
英文别名 更多

 2-氨基-3-(4-氯苯甲酰基)-4,5-二甲基噻吩物理化学性质

密度 1.303±0.06g/ml(Predicted)
沸点 435.4±45.0℃(Predicted)
分子式 C13H12ClNOS
分子量 265.75800
精确质量 265.03300
PSA 71.33000
LogP 4.41270
InChIKey FZCFEGHYRWGCEB-UHFFFAOYSA-N
SMILES Cc1sc(N)c(C(=O)c2ccc(Cl)cc2)c1C
储存条件 室温,干燥,密封

 2-氨基-3-(4-氯苯甲酰基)-4,5-二甲基噻吩安全信息

海关编码 2934999090

 2-氨基-3-(4-氯苯甲酰基)-4,5-二甲基噻吩合成线路

~70%

2-氨基-3-(4-氯苯甲酰基)-4,5-二甲基噻吩结构式

2-氨基-3-(4-氯苯甲酰基...

50508-66-2

文献:DANA-FARBER CANCER INSTITUTE, INC.; BRADNER, James, Elliott; MATZUK, Martin; QI, Jun Patent: WO2011/143657 A1, 2011 ; Location in patent: Page/Page column 78 ;

 2-氨基-3-(4-氯苯甲酰基)-4,5-二甲基噻吩上下游产品

2-氨基-3-(4-氯苯甲酰基)-4,5-二甲基噻吩上游产品  2

2-氨基-3-(4-氯苯甲酰基)-4,5-二甲基噻吩下游产品  1

 2-氨基-3-(4-氯苯甲酰基)-4,5-二甲基噻吩海关

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-(4-氯苯甲酰基)-4,5-二甲基噻吩靶点实验

查看更多实验

实验名称:Percentage of response to 10 uM of PD-81723 on CHO cells expressing the cloned human ...
来源:ChEMBL
靶标:Adenosine receptor A1
External Id:CHEMBL619493
实验名称:Discovery of Small Molecules to Inhibit Human Cytomegalovirus Nuclear Egress
来源:ICCB-Longwood/NSRB Screening Facility, Harvard Medical School
靶标:HCMV UL50
External Id:HMS1262
实验名称:Enhancing activity at 10 uM PD 81,723 (100%) at Adenosine A1 receptor in rat brain co...
来源:ChEMBL
靶标:Adenosine receptor A1
External Id:CHEMBL636818
实验名称:Dicer-mediated maturation of pre-microRNA
来源:Center for Chemical Genomics, University of Michigan
靶标:N/A
External Id:TargetID_659_CEMA
实验名称:Screen for inhibitors of RMI FANCM (MM2) intereaction
来源:11908
靶标:N/A
External Id:RMI-FANCM-MM2
实验名称:Percentage of response to 10 uM of PD-81723 on CHO cells expressing the cloned human ...
来源:ChEMBL
靶标:Adenosine receptor A1
External Id:CHEMBL619500
实验名称:Antagonistic activity expressed as percent displacement of 0.4 nM of [3H]DPCPX from a...
来源:ChEMBL
靶标:Adenosine receptor A1
External Id:CHEMBL638633
实验名称:Inhibition of wild type recombinant human RET at 100 uM using peptide as substrate by...
来源:ChEMBL
靶标:Proto-oncogene tyrosine-protein kinase receptor Ret
External Id:CHEMBL4231189
实验名称:High-throughput screen for inhibitors of the GIV GBA-motif interaction with Galpha-i ...
来源:ICCB-Longwood/NSRB Screening Facility, Harvard Medical School
External Id:HMS1303
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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 2-氨基-3-(4-氯苯甲酰基)-4,5-二甲基噻吩英文别名

(2-amino-4,5-dimethylthiophen-3-yl)(4-chlorophenyl)methanone
HMS1450D20
(2-amino-4,5-dimethyl-3-thienyl)-(4-chloro-phenyl)methanone
2-amino-3-(4-chlorobenzoyl)-4,5-dimethylthiophene
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