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6-氯-2-甲硫基-1H-苯并咪唑

更新时间:2025-08-23 17:14:22

6-氯-2-甲硫基-1H-苯并咪唑结构式
6-氯-2-甲硫基-1H-苯并咪唑结构式
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常用名 6-氯-2-甲硫基-1H-苯并咪唑 英文名 5-chloro-2-methylsulfanyl-3H-benzoimidazole
CAS号 7692-57-1 分子量 198.67300
密度 1.43g/cm3 沸点 381.6ºC at 760 mmHg
分子式 C8H7ClN2S 熔点 N/A
MSDS N/A 闪点 184.6ºC

 6-氯-2-甲硫基-1H-苯并咪唑名称

中文名 6-氯-2-甲硫基-1H-苯并咪唑
英文名 6-chloro-2-methylsulfanyl-1H-benzimidazole
英文别名 更多

 6-氯-2-甲硫基-1H-苯并咪唑物理化学性质

密度 1.43g/cm3
沸点 381.6ºC at 760 mmHg
分子式 C8H7ClN2S
分子量 198.67300
闪点 184.6ºC
精确质量 198.00200
PSA 53.98000
LogP 2.93820
InChIKey ZYJPSJQXODTXBZ-UHFFFAOYSA-N
SMILES CSc1nc2ccc(Cl)cc2[nH]1
折射率 1.701

 6-氯-2-甲硫基-1H-苯并咪唑安全信息

海关编码 2933990090

 6-氯-2-甲硫基-1H-苯并咪唑上下游产品

6-氯-2-甲硫基-1H-苯并咪唑上游产品  3

6-氯-2-甲硫基-1H-苯并咪唑下游产品  0

 6-氯-2-甲硫基-1H-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%

 6-氯-2-甲硫基-1H-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:The compound was tested in vitro against the protozoa Giardia lamblia, for the inhibi...
来源:ChEMBL
靶标:Giardia intestinalis
External Id:CHEMBL682614
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: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: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
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 6-氯-2-甲硫基-1H-苯并咪唑英文别名

2-Mercaptomethyl-5-chlor-benzimidazol
5-Chloro-1H-benzimidazol-2-yl methyl sulfide
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