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63762-81-2

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63762-81-2 Usage

Structure

A derivative of benzene with a fluorine atom, a methoxy group, a methyl group, and a nitro group.

Applications

Commonly used in the synthesis of other organic compounds and in the pharmaceutical industry.

Chemical properties

Useful intermediate in the production of various chemicals and pharmaceuticals.

Versatility

Presence of fluorine, methoxy, methyl, and nitro groups provides a range of diverse properties.

Industrial applications

Utilized in pharmaceuticals, agrochemicals, and materials science.

Check Digit Verification of cas no

The CAS Registry Mumber 63762-81-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,3,7,6 and 2 respectively; the second part has 2 digits, 8 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 63762-81:
(7*6)+(6*3)+(5*7)+(4*6)+(3*2)+(2*8)+(1*1)=142
142 % 10 = 2
So 63762-81-2 is a valid CAS Registry Number.

63762-81-2SDS

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 1-fluoro-2-methoxy-4-methyl-5-nitrobenzene

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:63762-81-2 SDS

63762-81-2Relevant articles and documents

THIAZOLIDINONE COMPOUNDS AND USE THEREOF

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Paragraph 0161-0162, (2017/09/21)

A pharmaceutical composition containing a compound of Formula (I) for treating an opioid receptor-associated condition. Also disclosed is a method for treating an opioid receptor-associated condition using such a compound. Further disclosed are two sets of thiazolidinone compounds of formula (I): (i) compounds each having an enantiomeric excess greater than 90% and (ii) compounds each being substituted with deuterium.

Synthesis and GABA-receptor binding activity of two fluoroaminomethylphenols

Honore,Hjeds

, p. 285 - 287 (2007/10/05)

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