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5302-77-2

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5302-77-2 Usage

General Description

6-methoxynaphthalen-1-amine is an organic compound with a naphthalene backbone and an amino group substitution at the 1-position, as well as a methoxy group at the 6-position. It is commonly used in the field of chemical research and drug development. The compound is known for its potential pharmaceutical applications, particularly in the synthesis of various medicinal and pharmaceutical intermediates. It is also used as a building block in the production of various dyes and organic pigments. Additionally, it has been studied for its potential as an active ingredient in the development of novel drugs targeting specific diseases and medical conditions.

Check Digit Verification of cas no

The CAS Registry Mumber 5302-77-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,3,0 and 2 respectively; the second part has 2 digits, 7 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 5302-77:
(6*5)+(5*3)+(4*0)+(3*2)+(2*7)+(1*7)=72
72 % 10 = 2
So 5302-77-2 is a valid CAS Registry Number.
InChI:InChI=1/C19H22N2O5/c1-5-26-17-10-14(21(24)25)8-12(18(17)23)11-20-15-9-13(19(2,3)4)6-7-16(15)22/h6-11,20,22H,5H2,1-4H3/b12-11+

5302-77-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name 6-methoxynaphthalen-1-amine

1.2 Other means of identification

Product number -
Other names 1-amino-6-methoxynaphthalene

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:5302-77-2 SDS

5302-77-2Relevant articles and documents

A new access to 1-naphthylamines by an equivalent Semmler-Wolff reaction

Janin,Bisagni

, p. 57 - 59 (2007/10/02)

A new access to 1-naphthylamines from the corresponding 3,4-dihydro-1(2H)-naphthalenones (α-tetralones) is described. It proceeds in a two-step sequence: preparation of the benzyl Schiff's base of an α-tetralone followed by aromatization over palladium ca

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