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1H-INDOLE,3-(2-BROMOETHYL)-6-FLUORO is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

325773-41-9

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325773-41-9 Usage

Structure

An indole derivative with a bromoethyl group at the 3 position and a fluorine atom at the 6 position.

Usage

In organic synthesis and medicinal chemistry as a building block for the synthesis of various biologically active molecules.

Potential applications

Pharmaceutical applications due to its structural features.

Use as a starting material

In the production of pharmaceuticals and agrochemicals.

Note

Specific uses and properties may vary depending on the application and intended use.

Check Digit Verification of cas no

The CAS Registry Mumber 325773-41-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,2,5,7,7 and 3 respectively; the second part has 2 digits, 4 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 325773-41:
(8*3)+(7*2)+(6*5)+(5*7)+(4*7)+(3*3)+(2*4)+(1*1)=149
149 % 10 = 9
So 325773-41-9 is a valid CAS Registry Number.

325773-41-9SDS

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 3-(2-bromoethyl)-6-fluoroindole

1.2 Other means of identification

Product number -
Other names 1H-INDOLE,3-(2-BROMOETHYL)-6-FLUORO

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:325773-41-9 SDS

325773-41-9Downstream Products

325773-41-9Relevant academic research and scientific papers

SMALL MOLECULE INDUCERS OF GDNF AS POTENTIAL NEW THERAPEUTICS FOR NEUROPSYCHIATRIC DISORDERS

-

, (2013/03/26)

The invention provides a compound having the structure (I), wherein A is a substituted or unsubstituted ring; Z is present or absent and when present is (II), wherein n is 0, 1, 2, 3, or 4; Y is -(CR11R12)-, -NH(CR11R12)- or -O(CR11R12)- wherein R11 and R12 are each hydrogen or combine to form a carbonyl; and wherein R1 to R10 are herein as described.

Synthesis and pharmacological evaluation of aminopyrimidine series of 5-HT1A partial agonists

Dounay, Amy B.,Barta, Nancy S.,Bikker, Jack A.,Borosky, Susan A.,Campbell, Brian M.,Crawford, Terry,Denny, Lynne,Evans, Lori M.,Gray, David L.,Lee, Pil,Lenoir, Edward A.,Xu, Wenjian

scheme or table, p. 1159 - 1163 (2009/08/07)

Aminopyrimidine 2 (4-(1-(2-(1H-indol-3-yl)ethyl)piperidin-3-yl)-N-cyclopropylpyrimidin-2-amine) emerged from a high throughput screen as a novel 5-HT1A agonist. This compound showed moderate potency for 5-HT1A in binding and functional assays, as well as moderate metabolic stability. Implementation of a strategy for improving metabolic stability by lowering the lipophilicity (c Log D) led to identification of methyl ether 31 (4-(1-(2-(1H-indol-3-yl)ethyl)piperidin-3-yl)-N-(2-methoxyethyl)pyrimidin-2-amine) as a substantially improved compound within the series.

3-Thio-1,2,4-triazoles, novel somatostatin sst2/sst5 agonists

Contour-Galcera, Marie-Odile,Sidhu, Alban,Plas, Pascale,Roubert, Pierre

, p. 3555 - 3559 (2007/10/03)

Novel 3-thio-1,2,4-triazoles have been obtained via a solution-phase parallel synthesis strategy, affording potent non-peptidic human somatostatin receptor subtypes 2 and 5 agonists.

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