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2341-25-5

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2341-25-5 Usage

General Description

6-Fluoroindole-3-acetonitrile is a chemical compound with the molecular formula C10H8FNO. It is a derivative of indole, with a fluorine atom attached to the 6th carbon and an acetonitrile group attached to the 3rd carbon. 6-fluoroindole-3-acetonitrile is commonly used as an intermediate in the synthesis of pharmaceuticals, agrochemicals, and organic compounds. It has potential applications in the development of new drugs and as a building block in organic chemistry reactions. The presence of the fluoro and acetonitrile groups in 6-fluoroindole-3-acetonitrile imparts certain chemical and biological properties that make it valuable for various research and industrial purposes.

Check Digit Verification of cas no

The CAS Registry Mumber 2341-25-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,3,4 and 1 respectively; the second part has 2 digits, 2 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 2341-25:
(6*2)+(5*3)+(4*4)+(3*1)+(2*2)+(1*5)=55
55 % 10 = 5
So 2341-25-5 is a valid CAS Registry Number.
InChI:InChI=1/C10H7FN2/c11-8-1-2-9-7(3-4-12)6-13-10(9)5-8/h1-2,5-6,13H,3H2

2341-25-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-(6-fluoro-1H-indol-3-yl)acetonitrile

1.2 Other means of identification

Product number -
Other names 6-fluoroindole-3-acetonitrile

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:2341-25-5 SDS

2341-25-5Relevant articles and documents

Stereoselective Cascade Cyclizations with Samarium Diiodide to Tetracyclic Indolines: Precursors of Fluorostrychnines and Brucine

Beemelmanns, Christine,Nitsch, Dominik,Bentz, Christoph,Reissig, Hans-Ulrich

, p. 8780 - 8789 (2019)

A series of γ-indolylketones with fluorine, cyano or alkoxy substituents at the benzene moiety was prepared and subjected to samarium diiodide-promoted cyclization reactions. The desired dearomatizing ketyl cascade reaction forming two new rings proceeded

A NOVEL PROCESS FOR THE PREPARATION OF TRYPTAMINES AND DERIVATIVES THEREOF

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Page/Page column 22; 23, (2017/05/10)

The present invention relates to a novel process for the preparation of tryptamine, its substituted derivatives and intermediates for the preparation of them.

NEW DERIVATIVES OF INDOLE FOR THE TREATMENT OF CANCER, VIRAL INFECTIONS AND LUNG DISEASES

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Page/Page column 45, (2014/06/24)

The present invention relates to a new class of indole derivatives, having a particular MKlp2 inhibition profile and useful as a therapeutic agent, in particular for the treatment of cancer, viral infections and lung diseases.

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