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2-(哌啶-3-基)-1H-苯并[d]咪唑

更新时间:2025-09-20 17:14:10

2-(哌啶-3-基)-1H-苯并[d]咪唑结构式
2-(哌啶-3-基)-1H-苯并[d]咪唑结构式
品牌特惠专场
常用名 2-(哌啶-3-基)-1H-苯并[d]咪唑 英文名 2-(3-Piperidinyl)-1H-benzimidazole
CAS号 123771-23-3 分子量 201.26800
密度 1.167g/cm3 沸点 441.3ºC at 760mmHg
分子式 C12H15N3 熔点 N/A
MSDS N/A 闪点 220.7ºC

 2-(哌啶-3-基)-1H-苯并[d]咪唑名称

中文名 2-(3-哌啶基)-1H-苯并咪唑
英文名 2-(Piperidin-3-yl)-1H-benzo[d]imidazole
中文别名 2-哌啶-3-基-1H-苯并咪唑
英文别名 更多

 2-(哌啶-3-基)-1H-苯并[d]咪唑物理化学性质

密度 1.167g/cm3
沸点 441.3ºC at 760mmHg
分子式 C12H15N3
分子量 201.26800
闪点 220.7ºC
精确质量 201.12700
PSA 40.71000
LogP 2.35870
InChIKey LQZIJJKVPOTLRE-UHFFFAOYSA-N
SMILES c1ccc2[nH]c(C3CCCNC3)nc2c1
外观性状 浅棕色至棕色固体
蒸汽压 5.48E-08mmHg at 25°C
折射率 1.628
储存条件 2-8°C, 避光, 惰性气体

 2-(哌啶-3-基)-1H-苯并[d]咪唑安全信息

危害码 (欧洲) Xi
海关编码 2933990090

 2-(哌啶-3-基)-1H-苯并[d]咪唑合成线路

~47%

2-(哌啶-3-基)-1H-苯并[d]咪唑结构式

2-(哌啶-3-基)-1H-苯...

123771-23-3

文献:Wahlgren, Curtis G.; Addison, Anthony W. Journal of Heterocyclic Chemistry, 1989 , vol. 26, p. 541 - 543

 2-(哌啶-3-基)-1H-苯并[d]咪唑上下游产品

2-(哌啶-3-基)-1H-苯并[d]咪唑上游产品  2

2-(哌啶-3-基)-1H-苯并[d]咪唑下游产品  0

 2-(哌啶-3-基)-1H-苯并[d]咪唑海关

海关编码 2933990090
中文概述 2933990090. 其他仅含氮杂原子的杂环化合物. 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, 乌洛托品请注明外观, 6-己内酰胺请注明外观, 签约日期
Summary 2933990090. heterocyclic compounds with nitrogen hetero-atom(s) only. VAT:17.0%. Tax rebate rate:13.0%. . MFN tariff:6.5%. General tariff:20.0%

 2-(哌啶-3-基)-1H-苯并[d]咪唑靶点实验

查看更多实验

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:Screen for inhibitors of RMI FANCM (MM2) intereaction
来源:11908
靶标:N/A
External Id:RMI-FANCM-MM2
实验名称:Chemical Probes of Kaposi's Sarcoma Herpes Virus Latent Infection
来源:ICCB-Longwood/NSRB Screening Facility, Harvard Medical School
靶标:ORF 73 [Human herpesvirus 8 type M]
External Id:HMS791
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
实验名称:Cell-based high throughput primary assay to identify activators of GPR151
来源:The Scripps Research Institute Molecular Screening Center
靶标:RecName: Full=G-protein coupled receptor 151; AltName: Full=G-protein coupled receptor PGR7; AltName: Full=GPCR-2037; AltName: Full=Galanin receptor 4; AltName: Full=Galanin-receptor-like protein; Short=GalRL
External Id:GPR151_PHUNTER_AG_LUMI_1536_1X%ACT
实验名称:AlphaScreen-based biochemical high throughput primary assay to identify activators of...
来源:The Scripps Research Institute Molecular Screening Center
靶标:N/A
External Id:FBW7_ACT_ALPHA_1536_1X%ACT PRUN
实验名称:AlphaScreen-based biochemical high throughput primary assay to identify inhibitors of...
来源:The Scripps Research Institute Molecular Screening Center
External Id:MITF_INH_Alpha_1536_1X%INH PRUN
实验名称:A screen for compounds that inhibit viral RNA polymerase binding and polymerization a...
来源:ICCB-Longwood/NSRB Screening Facility, Harvard Medical School
靶标:Chain A, Poliovirus Polymerase With Gtp
External Id:HMS750
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 2-(哌啶-3-基)-1H-苯并[d]咪唑英文别名

2-piperidin-3-yl-1H-benzimidazole
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