跳转至内容
Merck
所有图片(1)

主要文件

查看所有文档

M14943

Sigma-Aldrich

5-甲氧基吲哚-3-甲醛

≥99%

别名:

3-Formyl-5-methoxyindole, NSC 521754

登录查看公司和协议定价

选择尺寸

1 G
$176.00

$176.00

请联系客服了解存货情况
获取大包装报价
所有图片(1)

选择尺寸

变更视图
1 G
$176.00

About This Item

经验公式（希尔记法）:
C10H9NO2
CAS号:
10601-19-1
分子量:
175.18
Beilstein:
132769
EC號碼:
234-220-5
MDL號碼:
MFCD00005623
分類程式碼代碼:
12352100
PubChem物質ID:
24896652
NACRES:
NA.22

$176.00

请联系客服了解存货情况
获取大包装报价

化驗

≥99%

mp

179-183 °C (lit.)

SMILES 字串

COc1ccc2[nH]cc(C=O)c2c1

InChI

1S/C10H9NO2/c1-13-8-2-3-10-9(4-8)7(6-12)5-11-10/h2-6,11H,1H3

InChI 密鑰

TUWARWGEOHQXCO-UHFFFAOYSA-N

正在寻找类似产品? 访问 产品对比指南

相关类别

應用

  • reactant in synthesis of tryptophan dioxygenase inhibitors as potential anticancer immunomodulators[1]
  • reactant in preparation of inhibitor of the C-terminal domain of RNA polymerase II
  • reactant in preparation of imidazopyridines and imidazobenzothiazoles[2]
  • reactant in preparation of fluorescent neuroactive probes for brain imaging[3]
  • reactant in preparation of antibacterial agents[4]
  • reactant in synthesis of antiandrogens[5]

象形圖

Exclamation mark
GHS07

訊號詞

Warning

危險聲明

H315,H319,H335

危險分類

Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

標靶器官

Respiratory system

儲存類別代碼

11 - Combustible Solids

水污染物質分類（WGK）

WGK 3

閃點（°F）

Not applicable

閃點（°C）

Not applicable

历史批次信息供参考:

分析证书(COA)

Lot/Batch Number
01118DJ
07105HH
S42217
07102TC
08823AC

没有发现合适的版本？

如果您需要特殊版本，可通过批号或批次号查找具体证书。

搜索COA

已有该产品？

在文件库中查找您最近购买产品的文档。

访问文档库

Adrienne S Brown et al.
Organic & biomolecular chemistry, 9(7), 2142-2148 (2011-02-05)
A set of spectrally diverse stilbazolium dyes was identified in an uptake assay using cultured brainstem and cerebellum cells isolated from e19 chicks. Pretreatment of cells with indatraline, a monoamine reuptake inhibitor, allowed identification of dyes that may interact with
Jinming Zhou et al.
Investigational new drugs, 28(3), 291-298 (2009-04-25)
A crucial event in prostate cancer progression is the transition from a hormone-sensitive to a lethal castration-refractory disease state. The antagonist-to-agonist conversion due to mutation in AR is a critical problem with the current clinically used antiandrogens. We aim to
Shuhong Wu et al.
Journal of medicinal chemistry, 54(8), 2668-2679 (2011-03-30)
To optimize the antitumor activity of oncrasin-1, a small molecule RNA polymerase II inhibitor, we evaluated 69 oncrasin-1 analogues for their cytotoxic activity against normal human epithelial cells and K-Ras mutant tumor cells. About 40 of those compounds were as
Taleb H Al-Tel et al.
European journal of medicinal chemistry, 46(5), 1874-1881 (2011-03-19)
New antimicrobial agents, imidazo[1,2-a]pyridine and imidazo[2,1-b][1,3]benzothiazole, have been synthesized. Their antimicrobial activities were conducted against various Gram-positive, Gram-negative bacteria and fungi. Compounds 6c, 7a, 10b, 11a, 12b, 14a, 14b, 15a and 15b, exerted strong inhibition of the investigated bacterial and
Anas J M Rasras et al.
European journal of medicinal chemistry, 45(6), 2307-2313 (2010-02-26)
Synthesis and antimicrobial activity of cholic acid analogues 4a-t are reported. The synthesis of 4a-t was accomplished from ethylcholate 2. The hydrazone moiety was introduced via coupling of the cholic acid hydrazide (3) with appropriately functionalized aldehyde utilizing acetic acid
查看所有相关文献

Questions

Reviews

No rating value

Active Filters

我们的科学家团队拥有各种研究领域经验，包括生命科学、材料科学、化学合成、色谱、分析及许多其他领域.

联系客户支持