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(1,2-dimethylindol-3-yl)-phenyl-methanone

更新时间:2025-08-25 17:23:20

(1,2-dimethylindol-3-yl)-phenyl-methanone结构式
(1,2-dimethylindol-3-yl)-phenyl-methanone结构式
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常用名 (1,2-dimethylindol-3-yl)-phenyl-methanone 英文名 (1,2-dimethylindol-3-yl)-phenyl-methanone
CAS号 59411-02-8 分子量 249.30700
密度 1.09g/cm3 沸点 399.7ºC at 760 mmHg
分子式 C17H15NO 熔点 N/A
MSDS N/A 闪点 195.5ºC

 名称

英文名 (1,2-dimethylindol-3-yl)-phenylmethanone
英文别名 更多

 物理化学性质

密度 1.09g/cm3
沸点 399.7ºC at 760 mmHg
分子式 C17H15NO
分子量 249.30700
闪点 195.5ºC
精确质量 249.11500
PSA 22.00000
LogP 3.71770
InChIKey MABIPSJHBDNCKH-UHFFFAOYSA-N
SMILES Cc1c(C(=O)c2ccccc2)c2ccccc2n1C
折射率 1.599

 合成线路

~90%

(1,2-dimethylindol-3-yl)-phenyl-methanone结构式

(1,2-dimethylin...

59411-02-8

文献:Wang, Lu; Li, Guijie; Liu, Yuanhong Organic Letters, 2011 , vol. 13, # 15 p. 3786 - 3789

~89%

(1,2-dimethylindol-3-yl)-phenyl-methanone结构式

(1,2-dimethylin...

59411-02-8

文献:Ma, Yuanhong; You, Jingsong; Song, Feijie Chemistry - A European Journal, 2013 , vol. 19, # 4 p. 1189 - 1193

~73%

(1,2-dimethylindol-3-yl)-phenyl-methanone结构式

(1,2-dimethylin...

59411-02-8

文献:Yu, Lin; Li, Pinhua; Wang, Lei Chemical Communications, 2013 , vol. 49, # 23 p. 2368 - 2370

~70%

(1,2-dimethylindol-3-yl)-phenyl-methanone结构式

(1,2-dimethylin...

59411-02-8

文献:Shafiee, A.; Sattari, S. Synthesis, 1981 , # 5 p. 389 - 390

~%

(1,2-dimethylindol-3-yl)-phenyl-methanone结构式

(1,2-dimethylin...

59411-02-8

文献:Xia, Xiao-Feng; Zhang, Lu-Lu; Song, Xian-Rong; Niu, Yan-Ning; Liu, Xue-Yuan; Liang, Yong-Min Chemical Communications, 2013 , vol. 49, # 14 p. 1410 - 1412

~%

(1,2-dimethylindol-3-yl)-phenyl-methanone结构式

(1,2-dimethylin...

59411-02-8

文献:Akguen, Eyuep; Tunali, Mustafa; Pindur, Ulf Archiv der Pharmazie (Weinheim, Germany), 1987 , vol. 320, # 5 p. 397 - 401

~%

(1,2-dimethylindol-3-yl)-phenyl-methanone结构式

(1,2-dimethylin...

59411-02-8

文献:Yu, Lin; Li, Pinhua; Wang, Lei Chemical Communications, 2013 , vol. 49, # 23 p. 2368 - 2370

 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: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
实验名称:Antibacterial activity against Klebsiella pneumoniae MDR ATCC 70063 (CO-ADD:GN_003); ...
来源:ChEMBL
靶标:Klebsiella pneumoniae
External Id:CHEMBL4296186
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:Identifying Sarm1 TIR NADase inhibitors through high throughput HPLC assay
来源:24386
靶标:N/A
External Id:Sarm1 TIR NADase inhibitors
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 英文别名

(1,2-dimethyl-indol-3-yl)-phenyl-methanone
HMS2886L03
3-Benzoyl-1,2-dimethylindol
1,2-Dimethyl-3-benzoyl-indol
(1,2-dimethyl-1h-indol-3-yl)(phenyl)methanone
1,2-dimethyl-3-benzoylindole
3-Benzoyl-1,2-dimethylindole
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