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2-(4-哌啶基)-1,3-苯并噻唑

更新时间:2025-08-27 19:09:58

2-(4-哌啶基)-1,3-苯并噻唑结构式
2-(4-哌啶基)-1,3-苯并噻唑结构式
品牌特惠专场
常用名 2-(4-哌啶基)-1,3-苯并噻唑 英文名 2-(Piperidin-4-yl)benzo[d]thiazole
CAS号 51784-73-7 分子量 218.31800
密度 1.288g/cm3 沸点 393ºC at 760mmHg
分子式 C12H14N2S 熔点 102-105 °C
MSDS N/A 闪点 188.4ºC

 2-(4-哌啶基)-1,3-苯并噻唑名称

中文名 2-(4-哌啶基)-1,3-苯并噻唑
英文名 2-piperidin-4-yl-1,3-benzothiazole
英文别名 更多

 2-(4-哌啶基)-1,3-苯并噻唑物理化学性质

密度 1.288g/cm3
沸点 393ºC at 760mmHg
熔点 102-105 °C
分子式 C12H14N2S
分子量 218.31800
闪点 188.4ºC
精确质量 218.08800
PSA 53.16000
LogP 3.09210
InChIKey CYASANLJWAJEPW-UHFFFAOYSA-N
SMILES c1ccc2sc(C3CCNCC3)nc2c1
折射率 1.629
储存条件 2-8°C

 2-(4-哌啶基)-1,3-苯并噻唑MSDS

 2-(4-哌啶基)-1,3-苯并噻唑安全信息

危害码 (欧洲) Xi
海关编码 2934999090

 2-(4-哌啶基)-1,3-苯并噻唑合成线路

~89%

2-(4-哌啶基)-1,3-苯并噻唑结构式

2-(4-哌啶基)-1,3-苯并噻唑

51784-73-7

文献:Orjales; Bordell; Rubio Journal of Heterocyclic Chemistry, 1995 , vol. 32, # 3 p. 707 - 718

~%

2-(4-哌啶基)-1,3-苯并噻唑结构式

2-(4-哌啶基)-1,3-苯并噻唑

51784-73-7

文献:Merck and Co., Inc. Patent: US6248755 B1, 2001 ; US 6248755 B1

~%

2-(4-哌啶基)-1,3-苯并噻唑结构式

2-(4-哌啶基)-1,3-苯并噻唑

51784-73-7

文献:WELFIDE CORPORATION Patent: EP1308439 A1, 2003 ;

 2-(4-哌啶基)-1,3-苯并噻唑上下游产品

2-(4-哌啶基)-1,3-苯并噻唑上游产品  4

2-(4-哌啶基)-1,3-苯并噻唑下游产品  0

 2-(4-哌啶基)-1,3-苯并噻唑海关

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-(4-哌啶基)-1,3-苯并噻唑靶点实验

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: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:Fluorescence-based cell-based primary high throughput screening assay to identify pos...
来源:The Scripps Research Institute Molecular Screening Center
靶标:muscarinic acetylcholine receptor M1 [Homo sapiens]
External Id:CHRM1_PAM_FLUO8_1536_1X%ACT PRUN
实验名称:Fluorescence polarization-based biochemical high throughput primary assay to identify...
来源:The Scripps Research Institute Molecular Screening Center
靶标:RecName: Full=Sialate O-acetylesterase; AltName: Full=H-Lse; AltName: Full=Sialic acid-specific 9-O-acetylesterase; Flags: Precursor [Homo sapiens]
External Id:SIAE_INH_FP_1536_1X%INH PRUN
实验名称:uHTS identification of small molecule modulators of NR3A
来源:Burnham Center for Chemical Genomics
靶标:N/A
External Id:SBCCG-A1015-NR3A-Primary-Assay
实验名称:uHTS identification of small molecule modulators of Rev-erb Alpha.
来源:Burnham Center for Chemical Genomics
靶标:N/A
External Id:SBCCG-A1016-RevErbaLBD-Primary-Assay
实验名称:MITF Measured in Cell-Based System Using Plate Reader - 2084-01_Activator_SinglePoint...
来源:Broad Institute
靶标:N/A
External Id:2084-01_Activator_SinglePoint_HTS_Activity
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 2-(4-哌啶基)-1,3-苯并噻唑英文别名

2-(piperidin-4-yl)benzo[d]thiazole
4-(2-benzothiazolyl)piperidine
4-(benzothiazol-2-yl)-piperidine
2-(4-piperidinyl)benzothiazole
2-(4-piperidyl)benzothiazole
4-(2-benzothiazolyl)-1-piperidine
2-(piperidin-4-yl)-1,3-benzothiazole
2-(4-piperidinyl)-1,3-benzothiazole
2-Piperidin-4-yl-benzothiazole
piperidinylbenzothiazole
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