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6-FLUORO-2,3,4,9-TETRAHYDRO-1H-CARBAZOLE-3-CARBOXYLIC ACID ETHYL ESTER is a complex chemical compound that belongs to the carbazole class of organic compounds. These compounds are known for their polycyclic aromatic hydrocarbon structure, featuring two benzene rings fused onto a five-membered nitrogen-containing ring. The inclusion of an ethyl ester functional group in its molecular structure indicates potential applications in organic synthesis. However, due to the lack of readily available information on its physical properties, toxicity levels, and specific uses in industrial or scientific contexts, 6-FLUORO-2,3,4,9-TETRAHYDRO-1H-CARBAZOLE-3-CARBOXYLIC ACID ETHYL ESTER may be considered relatively obscure or specialized.

322725-63-3

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322725-63-3 Usage

Uses

Due to the limited information provided, it is challenging to list specific applications for 6-FLUORO-2,3,4,9-TETRAHYDRO-1H-CARBAZOLE-3-CARBOXYLIC ACID ETHYL ESTER. However, based on its classification and molecular structure, it can be inferred that it may be used in the following ways:
Used in Organic Synthesis:
6-FLUORO-2,3,4,9-TETRAHYDRO-1H-CARBAZOLE-3-CARBOXYLIC ACID ETHYL ESTER is used as a chemical intermediate for the synthesis of more complex organic compounds, given its carbazole core and ethyl ester functional group.
Used in Research and Development:
In the scientific community, 6-FLUORO-2,3,4,9-TETRAHYDRO-1H-CARBAZOLE-3-CARBOXYLIC ACID ETHYL ESTER may be utilized as a subject of study in research projects aimed at understanding its properties, potential applications, and possible toxicity levels.
Used in Pharmaceutical Industry:
Although not explicitly mentioned, the carbazole class of compounds has been known to have pharmaceutical applications. Therefore, 6-FLUORO-2,3,4,9-TETRAHYDRO-1H-CARBAZOLE-3-CARBOXYLIC ACID ETHYL ESTER could potentially be used as a starting material or a component in the development of new drugs.
Used in Chemical Industry:
In the chemical industry, 6-FLUORO-2,3,4,9-TETRAHYDRO-1H-CARBAZOLE-3-CARBOXYLIC ACID ETHYL ESTER may serve as a raw material or a catalyst in the production of various chemical products, given its unique molecular structure.

Check Digit Verification of cas no

The CAS Registry Mumber 322725-63-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,2,2,7,2 and 5 respectively; the second part has 2 digits, 6 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 322725-63:
(8*3)+(7*2)+(6*2)+(5*7)+(4*2)+(3*5)+(2*6)+(1*3)=123
123 % 10 = 3
So 322725-63-3 is a valid CAS Registry Number.

322725-63-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name Ethyl 6-fluoro-2,3,4,9-tetrahydro-1H-carbazole-3-carboxylate

1.2 Other means of identification

Product number -
Other names 6-fluoro-2,3,4,9-tetrahydro-1H-carbazole-3-carboxylic acid ethyl ester

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:322725-63-3 SDS

322725-63-3Relevant academic research and scientific papers

First scale-up: Problems and resolutions on the synthesis of WAY-253752, a novel, dual-acting SSRI/5HT1A antagonist

Nikitenko, Antonia,Evrard, Deborah,Sabb, Annmarie L.,Vogel, Robert L.,Stack, Gary,Young, Mairead,Lin, Melissa,Harrison, Boyd L.,Potoski, John R.

, p. 76 - 80 (2008)

An alternative synthesis of WAY-253752, 1, a novel, dual-acting SSRI/5HT1A antagonist, was developed and used for the first scale-up. Initially, the target compound was synthesized as part of a diasteromeric mixture separated by chiral preparative HPLC. The new route was designed around intermediates suitable for chiral resolution, and its conditions were successfully determined.

Advances toward new antidepressants with dual serotonin transporter and 5-HT1A receptor affinity within a class of 3-aminochroman derivatives. Part 2

Hatzenbuhler, Nicole T.,Baudy, Reinhardt,Evrard, Deborah A.,Failli, Amedeo,Harrison, Boyd L.,Lenicek, Steven,Mewshaw, Richard E.,Saab, Annmarie,Shah, Uresh,Sze, Jean,Zhang, Minsheng,Zhou, Dahui,Chlenov, Michael,Kagan, Michael,Golembieski, Jeannette,Hornby, Geoffrey,Lai, Margaret,Smith, Deborah L.,Sullivan, Kelly M.,Schechter, Lee E.,Andree, Terrance H.

experimental part, p. 6980 - 7004 (2009/11/30)

Novel compounds combining a 5-HT1A moiety (3-aminochroman scaffold) and a 5-HT transporter (indole analogues) linked through a common basic nitrogen via an alkyl chain attached at the 1- or 3-position of the indole were evaluated for dual affin

CYCLOALKYLFUSED INDOLE, BENZOTHIOPHENE, BENZOFURAN AND INDENE DERIVATIVES

-

Page/Page column 34-35; 28, (2008/06/13)

The present invention provides cycloalkylfused indole, benzothiophene, benzofuran, and indene derivatives, and methods for using them to, for example, treat, prevent and/or ameliorate central nervous system diseases by antagonizing 5-HT1A receptors and mo

3-AMINO CHOMAN AND 2-AMINO TETRALIN DERIVATIVES

-

Page/Page column 76a, (2010/02/10)

3-Amino chroman and 2-amino tetralin derivatives and compositions containing such compounds are disclosed. Methods of using the 3-amino chroman and 2-amino tetralin compounds and compositions containing such compounds in the treatment of serotonin disorders, such as depression and anxiety, are also disclosed.

Discovery and optimization of a series of carbazole ureas as NPY5 antagonists for the treatment of obesity

Block, Michael H.,Boyer, Scott,Brailsford, Wayne,Brittain, David R.,Carroll, Debra,Chapman, Steve,Clarke, David S.,Donald, Craig S.,Foote, Kevin M.,Godfrey, Linda,Ladner, Anthony,Marsham, Peter R.,Masters, David J.,Mee, Christine D.,O'Donovan, Michael R.,Pease, J. Elizabeth,Pickup, Adrian G.,Rayner, John W.,Roberts, Andrew,Schofield, Paul,Suleman, Abid,Turnbull, Andrew V.

, p. 3509 - 3523 (2007/10/03)

The hypothesis that antagonists of the neuropeptide Y5 receptor would provide safe and effective appetite suppressants for the treatment of obesity has prompted vigorous research to identify suitable compounds. We discovered a series of acylated aminocarb

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