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144951-50-8

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144951-50-8 Usage

Chemical Class

The compound belongs to the indole class of heterocyclic compounds.

Structure

The compound contains an indole ring with a fluorine atom and a methyl group attached to it.

Usage

The compound is commonly used in the pharmaceutical and agrochemical industries as a building block for the synthesis of various biologically active molecules.

Applications

The compound has potential applications in the field of organic synthesis and materials science.

Unique Properties

The combination of the fluorine and methyl substituents in the indole ring gives this compound interesting chemical and biological properties.

Value

The compound is a valuable tool for the development of new drugs and agricultural chemicals.

Check Digit Verification of cas no

The CAS Registry Mumber 144951-50-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,4,9,5 and 1 respectively; the second part has 2 digits, 5 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 144951-50:
(8*1)+(7*4)+(6*4)+(5*9)+(4*5)+(3*1)+(2*5)+(1*0)=138
138 % 10 = 8
So 144951-50-8 is a valid CAS Registry Number.

144951-50-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name 1H-Indole,2-fluoro-1-methyl-(9CI)

1.2 Other means of identification

Product number -
Other names -

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:144951-50-8 SDS

144951-50-8Downstream Products

144951-50-8Relevant articles and documents

Fluoridation of heteroaromatic iodonium salts - Experimental evidence supporting theoretical prediction of the selectivity of the process

Martin-Santamaria, Sonsoles,Carroll, Michael A.,Carroll, Colm M.,Carter, Charles D.,Pike, Victor W.,Rzepa, Henry S.,Widdowson, David A.

, p. 649 - 650 (2000)

Theoretical prediction, that the nucleophilic substitution of a range of arylheteroaryliodonium salts by fluoride ion is regioselective for the aryl ring with the exception of benzo[b]furan, are borne out by experimental observation.

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