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文件

349593

6-氟吲哚

Name: 6-氟吲哚
Brand: ALDRICH

98%

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别名:

NSC 520436

经验公式（希尔记法）:

C₈H₆FN

CAS号:

399-51-9

分子量:

135.14

Beilstein:

112192

MDL编号:

MFCD00056933

PubChem化学物质编号:

24861689

NACRES:

NA.22

检测方案

98%

mp

72-76 °C (lit.)

SMILES字符串

Fc1ccc2cc[nH]c2c1

InChI

1S/C8H6FN/c9-7-2-1-6-3-4-10-8(6)5-7/h1-5,10H

InChI key

YYFFEPUCAKVRJX-UHFFFAOYSA-N

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一般描述

6-Fluoroindole is a halogen substituted indole. Experimental ionization potential of 6-fluoroindole has been evaluated. Preparation of 6-fluoroindole via nitration of indoline has been reported.

应用

6-Fluoroindole may be used as reactant in the preparation of:

tryptophan dioxygenase inhibitors pyridyl-ethenyl-indoles as potential anticancer immunomodulators
antibacterial agents
antifungal agents
Sodium-Dependent Glucose Co-transporter 2 (SGLT2) Inhibitors for the management of hyperglycemia in diabetes
potent selective serotonin reuptake inhibitors
inhibitors of HIV-1 attachment

象形图

GHS07

警示用语：

Warning

危险声明

H315 - H319 - H335

预防措施声明

P261 - P264 - P271 - P280 - P302 + P352 - P305 + P351 + P338

危险分类

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

靶器官

Respiratory system

储存分类代码

11 - Combustible Solids

WGK

WGK 3

闪点(°F)

Not applicable

闪点(°C)

Not applicable

个人防护装备

dust mask type N95 (US), Eyeshields, Gloves

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示例

T1503

货号

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包装规格/数量

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Full and Partial Agonism of a Designed Enzyme Switch.

S Jimmy Budiardjo et al.

ACS synthetic biology, 5(12), 1475-1484 (2016-07-09)

Chemical biology has long sought to build protein switches for use in molecular diagnostics, imaging, and synthetic biology. The overarching challenge for any type of engineered protein switch is the ability to respond in a selective and predictable manner that

Synthesis and structure-affinity relationships of novel small molecule natural product derivatives capable of discriminating between serotonin 5-HT1A, 5-HT2A, 5-HT2C receptor subtypes.

David F Cummings et al.

Bioorganic & medicinal chemistry, 18(13), 4783-4792 (2010-06-24)

Efforts to develop ligands that distinguish between clinically relevant 5-HT2A and 5-HT2C serotonin receptor subtypes have been challenging, because their sequences have high homology. Previous studies reported that a novel aplysinopsin belonging to a chemical class of natural products isolated

Na, Y. M.

Bull. Korean Chem. Soc., 31, 3467-3467 (2010)

3-(2-(3-Pyridinyl)thiazolidin-4-oyl)indoles, a novel series of platelet activating factor antagonists.

G S Sheppard et al.

Journal of medicinal chemistry, 37(13), 2011-2032 (1994-06-24)

(2RS,4R)-3-(2-(3-Pyridinyl)thiazolidin-4-oyl)indoles represent a new class of potent, orally active antagonists of platelet activating factor (PAF). The compounds were prepared by acylation of the magnesium or zinc salts of substituted indoles with (2RS,4R)-2-(3-pyridinyl)-3-(tert-butoxycarbonyl)thiazolidin-4-oyl chloride. The 3-acylindole moiety functions as a hydrolytically

Synthesis of 5-and 6-Halogenoindoles from Indoline

Ikan R, et al.

Israel J. Chem., 2(2), 37-42 (1964)

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