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5-FLUORO-1H-INDOLE-7-CARBALDEHYDE is a synthetic chemical compound with the molecular formula C9H7FNO. It is a derivative of the indole structure, featuring a fluorine atom at the 5-position and an aldehyde functional group at the 7-position of the indole ring. 5-FLUORO-1H-INDOLE-7-CARBALDEHYDE is recognized for its unique structure and reactivity, which makes it a valuable building block in the construction of complex organic molecules with potential medicinal properties. Its presence in organic synthesis and pharmaceutical research underscores its importance in the development of new drugs and bioactive molecules. Furthermore, 5-FLUORO-1H-INDOLE-7-CARBALDEHYDE has demonstrated various biological activities, positioning it as a significant target for exploration in medicinal chemistry and drug discovery.

603306-52-1

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603306-52-1 Usage

Uses

Used in Organic Synthesis:
5-FLUORO-1H-INDOLE-7-CARBALDEHYDE is utilized as a key intermediate in organic synthesis for the creation of complex organic molecules. Its distinctive structure and reactivity facilitate the synthesis of a variety of compounds with potential applications in different fields.
Used in Pharmaceutical Research:
In the pharmaceutical industry, 5-FLUORO-1H-INDOLE-7-CARBALDEHYDE serves as a crucial component in the development of new drugs and bioactive molecules. Its unique properties allow researchers to explore its potential in treating various diseases and conditions.
Used in Medicinal Chemistry:
5-FLUORO-1H-INDOLE-7-CARBALDEHYDE is employed as a building block in medicinal chemistry for the design and synthesis of novel compounds with therapeutic potential. Its biological activities make it an important candidate for further investigation and optimization to enhance its medicinal properties.
Used in Drug Discovery:
As a significant target in drug discovery, 5-FLUORO-1H-INDOLE-7-CARBALDEHYDE is explored for its potential to contribute to the development of innovative therapeutic agents. Its diverse biological activities suggest that it may play a role in addressing unmet medical needs.

Check Digit Verification of cas no

The CAS Registry Mumber 603306-52-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 6,0,3,3,0 and 6 respectively; the second part has 2 digits, 5 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 603306-52:
(8*6)+(7*0)+(6*3)+(5*3)+(4*0)+(3*6)+(2*5)+(1*2)=111
111 % 10 = 1
So 603306-52-1 is a valid CAS Registry Number.
InChI:InChI=1/C9H6FNO/c10-8-3-6-1-2-11-9(6)7(4-8)5-12/h1-5,11H

603306-52-1SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 5-FLUORO-1H-INDOLE-7-CARBALDEHYDE

1.2 Other means of identification

Product number -
Other names 5-Fluoro-7-formyl-1H-indole

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:603306-52-1 SDS

603306-52-1Relevant academic research and scientific papers

1,2-DIHYDRO-3H-PYRAZOL-3-ONE COMPOUNDS AND METHODS OF USING SAME

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Paragraph 0341; 0343, (2020/11/27)

The present disclosure relates to 1,2-dihydro-3H-pyrazol-3-one compounds and methods of using them to induce self-renewal of stem/progenitor supporting cells, including inducing the stem/progenitor cells to proliferate while maintaining, in the daughter c

METHODS FOR HAIR FOLLICLE STEM CELL PROLIFERATION

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, (2020/05/06)

The present invention relates to compositions of minoxidil and Sonic Hedgehog (Shh) pathway activators and optionally, Wnt agonists and methods of using them to induce self-renewal of hair follicle stem cells, including inducing the hair follicle stem cells to proliferate while maintaining, in the daughter cells, the capacity to differentiate into hair follicle epithelial cells.

1,2-DIHYDRO-3H-PYRAZOL-3-ONE COMPOUNDS AND METHODS OF USING SAME

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Paragraph 0293, (2019/07/13)

The present disclosure relates to l,2-dihydro-3H-pyrazol-3-one compounds and methods of using them to induce self-renewal of stem/progenitor supporting cells (e.g. cochlear cells), including inducing the stem/progenitor cells to proliferate while maintain

1,5-DIHYDRO-2H-PYRROL-2-ONE COMPOUNDS AND METHODS OF USING SAME

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Paragraph 0336-0338, (2018/08/20)

The present invention relates to 1,5-dihydro-2H-pyrrol-2-one compounds and methods of using them to induce self-renewal of stem/progenitor supporting cells, including inducing the stem/progenitor cells to proliferate while maintaining, in the daughter cells, the capacity to differentiate into tissue cells.

METHODS FOR HAIR FOLLICLE STEM CELL PROLIFERATION

-

Paragraph 0284, (2018/11/10)

The present invention relates to compositions of Sonic Hedgehog (Shh) pathway activators and Wnt agonists and methods of using them to induce self-renewal of hair follicle stem cells, including inducing the hair follicle stem cells to proliferate while maintaining, in the daughter cells, the capacity to differentiate into hair follicle epithelial cells.

1H-PYRROLE-2,5-DIONE COMPOUNDS AND METHODS OF USING THEM TO INDUCE SELF-RENEWAL OF STEM/PROGENITOR SUPPORTING CELLS

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, (2018/07/29)

The present invention relates to 1H-pyrrole-2,5-dione compounds and methods of using them to induce self-renewal of stem/progenitor supporting cells, including inducing the stem/progenitor cells to proliferate while maintaining, in the daughter cells, the capacity to differentiate into tissue cells.

POTENTIATION OF CANCER CHEMOTHERAPY

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Paragraph 0041, (2015/12/19)

An improved method for treating gastric cancer, ovarian cancer, non-small cell lung cancer, or colorectal cancer in a patient is described, as well as pharmaceutical compositions useful for the method and a process for preparing said compositions.

HEMATOPOIETIC NEOPLASM CHEMOTHERAPY

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, (2010/11/03)

A method and medicament for treating mixed lineage leukemia; translocated mixed lineage leukemia; translocated mixed lineage leukemia based acute myelogenous leukemia; translocated mixed lineage leukemia based acute lymphoid leukemia; a non-MLL based chronic myeloproliferative disorder, or non-MLL based acute lymphoid leukemia is provided.

BENZAZEPIN-2(1H)-ONE DERIVATIVES

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Page/Page column 46, (2008/06/13)

Compounds of formula (I) and pharmaceutically acceptable salts thereof are agonists at the beta-2 adrenoceptor. They are useful as feed additives for livestock animals.

Substituted 3-imidazo[1,2-a]pyridin-3-yl-4-(1,2,3,4-tetrahydro-[1,4] diazepino-[6,7,1-hi]indol-7-yl)pyrrole-2,5-diones as highly selective and potent inhibitors of glycogen synthase kinase-3

Engler, Thomas A.,Henry, James R.,Malhotra, Sushant,Cunningham, Brian,Furness, Kelly,Brozinick, Joseph,Burkholder, Timothy P.,Clay, Michael P.,Clayton, Joshua,Diefenbacher, Clive,Hawkins, Eric,Iversen, Philip W.,Li, Yihong,Lindstrom, Terry D.,Marquart, Angela L.,McLean, Johnathan,Mendel, David,Misener, Elizabeth,Briere, Daniel,O'Toole, John C.,Porter, Warren J.,Queener, Steven,Reel, Jon K.,Owens, Rebecca A.,Brier, Richard A.,Eessalu, Thomas E.,Wagner, Jill R.,Campbell, Robert M.,Vaughn, Renee

, p. 3934 - 3937 (2007/10/03)

Glycogen synthase kinase-3 (GSK3) is involved in signaling from the insulin receptor. Inhibitors of GSK3 are expected to effect lowering of plasma glucose similar to insulin, making GSK3 an attractive target for the treatment of type 2 diabetes. Herein we report the discovery of a series of potent and selective GSK3 inhibitors. Compounds 7-12 show oral activity in an in vivo model of type II diabetes, and 9 and 12 have desirable PK properties.

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