JavaScript 似乎在您的浏览器中禁用。 在我们的网站上获得最佳体验，请务必打开 Javascript 在您的浏览器。

为了获得访问"阿拉丁铁蛋"实时聊天框的流畅支持体验，建议您使用Chrome浏览器或选择360浏览器极速模式(如何切换极速模式?)，感谢您选择我们！

切换导航

我的购物车

搜索

6-甲氧基吲哚

规格或纯度: >98.0%(GC)

CAS编号: 3189-13-7
分子式: C₉H₉NO
分子量: 147.17
Beilstein号: 116483
EC号: 221-689-6
MDL号: MFCD00022780
PubChem编号: 76659

有货

库存信息

关闭

库存信息

关闭

库存信息

关闭

库存信息

关闭

库存信息

关闭

库存信息

关闭

货号 (SKU)	包装规格	是否现货	价格	数量
M123429-250mg	250mg	现货
M123429-1g	1g	现货
M123429-5g	5g	现货
M123429-10g	10g	期货
M123429-25g	25g	现货
M123429-100g	100g	现货

查看相关系列

五元杂环化合物吡咯类

Skip to the end of the images gallery

main product photo

Skip to the beginning of the images gallery

基本描述

别名	6-甲氧基吲哚
英文别名	NSC 92517 \| 6-Methoxy indole \| ethyl-o-toluate \| MLS000689267 \| STK893352 \| 4-Bromo Phthalic anhydride \| 6-Methoxy-1H-indole \| chloroxoquinoline \| 1H-Indol-6-yl methyl ether \| HMS2718O18 \| NCGC00245927-01 \| FT-0621193 \| 6-Methoxyindole \| AQ-776/40228276 \|
规格或纯度	>98.0%(GC)
英文名称	6-Methoxyindole
生化机理	6-Methoxyindole inhibits the chlorinating activity of myeloperoxidase and inhibits the generation of hypochlorous acid released by activated leukocytes.
储存温度	避光,充氩
运输条件	常规运输
产品介绍	Reactant for preparation of tryptophan dioxygenase inhibitors pyridyl-ethenyl-indoles as potential anticancer immunomodulators.and for synthesis of indolylindazoles and indolylpyrazolopyridines as interleukin-2 inducible T cell kinase inhibitors.and for preparation of diindolyloxyindoles as anticancer agents. Reactant for preparation of tryptophan dioxygenase inhibitors pyridyl-ethenyl-indoles as potential anticancer immunomodulators.and for synthesis of indolylindazoles and indolylpyrazolopyridines as interleukin-2 inducible T cell kinase inhibitors.and for preparation of diindolyloxyindoles as anticancer agents.

名称和标识符

EC号	221-689-6
IUPAC Name	6-methoxy-1H-indole
INCHI	InChI=1S/C9H9NO/c1-11-8-3-2-7-4-5-10-9(7)6-8/h2-6,10H,1H3
InChi Key	QJRWYBIKLXNYLF-UHFFFAOYSA-N
Canonical SMILES	COC1=CC2=C(C=C1)C=CN2
Isomeric SMILES	COC1=CC2=C(C=C1)C=CN2
WGK Germany	3
PubChem CID	76659
分子量	147.17
Beilstein号	116483
Reaxy-Rn	116483

化学和物理性质

敏感性	对光敏感，对空气敏感
沸点	105°C/0.2mm
熔点	90-94°C

安全和危险性（GHS）

象形图	Harmful
信号词	Warning
危险声明	H315: Causes skin irritation H319: Causes serious eye irritation H335: May cause respiratory irritation
预防措施声明	P261,P305+P351+P338,P280,P302+P352,P321,P405,P501,P264,P271,P304+P340,P403+P233,P362+P364,P264+P265,P337+P317,P332+P317,P319
WGK Germany	3
Reaxy-Rn	116483
个人防护装备	dust mask type N95 (US), Eyeshields, Gloves

质检证书(COA)

质检报告(COA)

输入批号以搜索COA:

相关文档

质检报告COA

请输入批号:

SDS中文版 SDS英文版

质量技术规格说明书

产品问答

产品问答

登录提交问题

您提交该产品问题后,我们会在1-2个工作日内给您答复,您可以登录"我的账号",然后点击"我的产品问答"查看答案

参考文献

1. Dolusić E, Larrieu P, Moineaux L, Stroobant V, Pilotte L, Colau D, Pochet L, Van den Eynde B, Masereel B, Wouters J et al.. (2011) Tryptophan 2,3-dioxygenase (TDO) inhibitors. 3-(2-(pyridyl)ethenyl)indoles as potential anticancer immunomodulators.. J Med Chem, 54 (15): (5320-34). [PMID:21726069]
2. R F Chen. (1968-06-01) Fluorescence of protonated excited-state forms of 5-hydroxytryptamine (serotonin) and related indoles.. Proceedings of the National Academy of Sciences of the United States of America, 60 ((2)): (598-605). [PMID:5303878]
3. Eugene L Piatnitski Chekler,Reeti Katoch-Rouse,Alexander S Kiselyov,Dan Sherman,Xiaohu Ouyang,Ki Kim,Ying Wang,Yaron R Hadari,Jacqueline F Doody. (2008-07-22) Synthesis and evaluation of heteroaryl-ketone derivatives as a novel class of VEGFR-2 inhibitors.. Bioorganic & medicinal chemistry letters, 18 ((15)): (4344-4347). [PMID:18640036]
4. Barry G Shearer, Hari S Patel, Andrew N Billin, James M Way, Deborah A Winegar, Millard H Lambert, Robert X Xu, Lisa M Leesnitzer, Raymond V Merrihew, Stephane Huet, Timothy M Willson,. (2008-08-30) Discovery of a novel class of PPARdelta partial agonists.. Bioorganic & medicinal chemistry letters, 18 ((18)): ( 5018-5022 ). [PMID:18722772]
5. Yu-Shan Wu,Mohane Selvaraj Coumar,Jang-Yang Chang,Hsu-Yi Sun,Fu-Ming Kuo,Ching-Chuan Kuo,Ying-Jun Chen,Chi-Yen Chang,Chia-Ling Hsiao,Jing-Ping Liou,Ching-Ping Chen,Hsien-Tsung Yao,Yi-Kun Chiang,Uan-Kang Tan,Chiung-Tong Chen,Chang-Ying Chu,Su-Ying Wu,Teng-Kuang Yeh,Chin-Yu Lin,Hsing-Pang Hsieh. (2009-07-10) Synthesis and evaluation of 3-aroylindoles as anticancer agents: metabolite approach.. Journal of medicinal chemistry, 52 ((15)): (4941-4945). [PMID:19586033]
6. Ahmed Kamal,Y V V Srikanth,M Naseer A Khan,Thokhir Basha Shaik,Md Ashraf. (2010-08-03) Synthesis of 3,3-diindolyl oxyindoles efficiently catalysed by FeCl3 and their in vitro evaluation for anticancer activity.. Bioorganic & medicinal chemistry letters, 20 ((17)): (5229-5231). [PMID:20673629]
7. Thomas Heine, Kathryn Tucker, Nonye Okonkwo, Berhanegebriel Assefa, Catleen Conrad, Anika Scholtissek, Michael Schlömann, George Gassner, Dirk Tischler,. (2016-11-11) Engineering Styrene Monooxygenase for Biocatalysis: Reductase-Epoxidase Fusion Proteins.. Applied biochemistry and biotechnology, 181 ((4)): ( 1590-1610 ). [PMID:27830466]
8. V F Ximenes,I M M Paino,O M M de Faria-Oliveira,L M da Fonseca,I L Brunetti. (2005-11-01) Indole ring oxidation by activated leukocytes prevents the production of hypochlorous acid.. Brazilian journal of medical and biological research = Revista brasileira de pesquisas medicas e biologicas, 38 ((11)): (1575-1583). [PMID:16258625]
9. Matthias Herdemann,Isabelle Heit,Frank-Uwe Bosch,Gianluca Quintini,Claudia Scheipers,Alexander Weber. (2010-10-23) Identification of potent ITK inhibitors through focused compound library design including structural information.. Bioorganic & medicinal chemistry letters, 20 ((23)): (6998-7003). [PMID:20965724]

上海阿拉丁生化科技股份有限公司

销售条款及条件隐私政策

© 2016 ALADDIN-E.COM . 版权所有,未经授权禁止拷贝本站资料,如有违反,将追究法律责任

沪公网安备 31012002004058号沪ICP备09093490号-2

本网站销售的所有产品仅用于工业应用或者科学研究等非医疗目的,不可用于人类或动物的临床诊断或者治疗,非药用,非食用。

危险品化学品经营许可证（带存储）

营业执照(三证合一)