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2-Amino-8-methoxy-1,2,3,4-tetrahydronaphthalene HCl, also known as AMTN HCl, is a synthetic chemical compound with a tetrahydronaphthalene core, which is part of the naphthalene family. This complex organic compound has an amino group (NH2) attached at the 2nd position and a methoxy group (OCH3) at the 8th position. The "HCl" indicates that the compound has been converted to a salt form, enhancing its solubility and ease of handling. Its applications can range from chemical research to pharmaceutical development and the preparation of complex organic molecules.

3880-76-0

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3880-76-0 Usage

Uses

Used in Chemical Research:
2-AMINO-8-METHOXY-1,2,3,4-TETRAHYDRONAPHTHALENE HCL is used as a research compound for studying its chemical properties and potential interactions with other molecules.
Used in Pharmaceutical Development:
2-AMINO-8-METHOXY-1,2,3,4-TETRAHYDRONAPHTHALENE HCL is used as a building block in the synthesis of pharmaceutical compounds, potentially contributing to the development of new drugs.
Used in Preparation of Complex Organic Molecules:
2-AMINO-8-METHOXY-1,2,3,4-TETRAHYDRONAPHTHALENE HCL is used as an intermediate in the synthesis of more complex organic molecules, facilitating the creation of advanced chemical structures.

Check Digit Verification of cas no

The CAS Registry Mumber 3880-76-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,8,8 and 0 respectively; the second part has 2 digits, 7 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 3880-76:
(6*3)+(5*8)+(4*8)+(3*0)+(2*7)+(1*6)=110
110 % 10 = 0
So 3880-76-0 is a valid CAS Registry Number.
InChI:InChI=1/C11H15NO.ClH/c1-13-11-4-2-3-8-5-6-9(12)7-10(8)11;/h2-4,9H,5-7,12H2,1H3;1H

3880-76-0SDS

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 2-AMINO-8-METHOXY-1,2,3,4-TETRAHYDRONAPHTHALENE HCL

1.2 Other means of identification

Product number -
Other names 8-Methoxy-1,2,3,4-tetrahydronaphthalen-2-aMine

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:3880-76-0 SDS

3880-76-0Relevant articles and documents

SUBSTITUTED 2-AMIDOTETRALINS AS MELATONIN AGONISTS AND ANTAGONISTS

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, (2008/06/13)

The present invention relates generally to compounds having melatonin receptor activities and in particular to substituted 2-amidotetralin derivatives; to pharmaceutical preparations comprising such compounds; and to methods for using these compounds as t

A new synthesis of 8-hydroxy-2-di-n-propylamino-tetralin (8-OH-DPAT)

Langlois,Gaudy

, p. 1723 - 1734 (2007/10/02)

A new synthesis method for 8-OH-DPAT, a specific agonist at the 5-HT(1A) serotonin receptor, is described. It employs the Curtius degradation of a tetralin carboxylic acid easily prepared from (2-methoxy benzyl) succinic acid by Friedel-Craft cyclisation.

SUBSTITUTED 2-AMIDOTETRALINS AS MELATONIN AGONISTS AND ANTAGONISTS

-

, (2008/06/13)

The present invention relates generally to compounds having melatonin receptor activities and in particular to substituted 2-amidotetralin derivatives; to pharmaceutical preparations comprising such compounds; and to methods for using these compounds as t

Substituted amino-5,6,7,8-tetrahydronaphthyl-oxyacetic acids, processes for their preparation and their use as medicaments

-

, (2008/06/13)

Antithrombotic, antiatherosclerotic and antiischaemic compounds of the formula STR1 in which R1 is STR2 or SO2 R4, R3 is aryl, substituted aryl, heteroaryl, aralkyl or the group STR3 R4 is aryl or sub

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