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2-羟甲基-5-氯苯并咪唑

更新时间:2025-08-27 18:06:12

2-羟甲基-5-氯苯并咪唑结构式
2-羟甲基-5-氯苯并咪唑结构式
品牌特惠专场
常用名 2-羟甲基-5-氯苯并咪唑 英文名 1H-Benzimidazole-2-methanol,6-chloro
CAS号 6953-65-7 分子量 182.60700
密度 1.51g/cm3 沸点 443.9ºC at 760 mmHg
分子式 C8H7ClN2O 熔点 206-208°C
MSDS N/A 闪点 222.2ºC

 2-羟甲基-5-氯苯并咪唑名称

中文名 (6-氯-1H-苯并咪唑-2-基)甲醇
英文名 (6-Chloro-1H-benzo[d]imidazol-2-yl)methanol
中文别名 2-羟甲基-5-氯苯并咪唑
英文别名 更多

 2-羟甲基-5-氯苯并咪唑物理化学性质

密度 1.51g/cm3
沸点 443.9ºC at 760 mmHg
熔点 206-208°C
分子式 C8H7ClN2O
分子量 182.60700
闪点 222.2ºC
精确质量 182.02500
PSA 48.91000
LogP 1.70860
InChIKey NIWRFQPRPJVQLO-UHFFFAOYSA-N
SMILES OCc1nc2ccc(Cl)cc2[nH]1
折射率 1.724
储存条件 2-8°C

 2-羟甲基-5-氯苯并咪唑毒性和生态

 2-羟甲基-5-氯苯并咪唑安全信息

危害码 (欧洲) Xi
危险品运输编码 NONH for all modes of transport
海关编码 2933990090

 2-羟甲基-5-氯苯并咪唑合成线路

~80%

2-羟甲基-5-氯苯并咪唑结构式

2-羟甲基-5-氯苯并咪唑

6953-65-7

文献:JANSSEN RandD IRELAND; TAHRI, Abdellah; VENDEVILLE, Sandrine Marie Helene; JONCKERS, Tim Hugo Maria; RABOISSON, Pierre Jean-Marie Bernard; HU, Lili; DEMIN, Samuël Dominique; COOYMANS, Ludwig Paul Patent: WO2014/60411 A1, 2014 ; Location in patent: Page/Page column 58 ;

 2-羟甲基-5-氯苯并咪唑上下游产品

2-羟甲基-5-氯苯并咪唑上游产品  2

2-羟甲基-5-氯苯并咪唑下游产品  2

 2-羟甲基-5-氯苯并咪唑海关

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-羟甲基-5-氯苯并咪唑靶点实验

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: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: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:Primary Screen Inhibitors of CD40 Signaling in BL2 Cells Measured in Cell-Based Syste...
来源:Broad Institute
靶标:N/A
External Id:7124-01_Inhibitor_SinglePoint_HTS_Activity
实验名称:qHTS of TDP-43 Inhibitors: NCGC Sytravon Library Screen
来源:NCGC
External Id:tdp43-p2-repeat
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 2-羟甲基-5-氯苯并咪唑英文别名

(6-chloro-1H-benzimidazol-2-yl)methanol
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