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1-[(3,5-dibromo-2-hydroxybenzyl)(methyl)amino]methylnaphthalen-2-ol is a complex organic chemical compound characterized by a naphthalen-2-ol core and a substituted benzylamine group. It features a naphthalene ring with a hydroxyl group at the 2 position and a methylamino substituent at the 1 position, which is connected to a 3,5-dibromo-2-hydroxybenzyl group. This unique structure suggests potential applications in pharmaceuticals and organic synthesis, offering opportunities for research and development in chemical and pharmaceutical sciences.

3534-74-5

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3534-74-5 Usage

Uses

Used in Pharmaceutical Industry:
1-[(3,5-dibromo-2-hydroxybenzyl)(methyl)amino]methylnaphthalen-2-ol is used as a pharmaceutical compound for its potential therapeutic properties. Its unique structure may contribute to the development of new drugs, particularly in the areas of medicinal chemistry and drug discovery.
Used in Organic Synthesis:
In the field of organic synthesis, 1-[(3,5-dibromo-2-hydroxybenzyl)(methyl)amino]methylnaphthalen-2-ol serves as a key intermediate or building block in the synthesis of more complex organic molecules. Its versatile chemical structure allows for further functionalization and modification, making it a valuable component in the creation of novel organic compounds with various applications.

Check Digit Verification of cas no

The CAS Registry Mumber 3534-74-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,5,3 and 4 respectively; the second part has 2 digits, 7 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 3534-74:
(6*3)+(5*5)+(4*3)+(3*4)+(2*7)+(1*4)=85
85 % 10 = 5
So 3534-74-5 is a valid CAS Registry Number.

3534-74-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-[[(3,5-dibromo-2-hydroxyphenyl)methyl-methylamino]methyl]naphthalen-2-ol

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

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More Details:3534-74-5 SDS

3534-74-5Downstream Products

3534-74-5Relevant academic research and scientific papers

Synthesis of dioxazaborocines from N-substituted-bis(2-hydroxyaryl)aminomethylamines

Woodgate, Paul D.,Horner, Gillian M.,Maynard, N. Paul,Rickard, Clifton E.F.

, p. 180 - 193 (2007/10/03)

The preparation of a number of tripodal amines from aminoalkylation of 1,3-benzoxazines by phenols is presented. A series of ligands prepared in this manner were successfully coordinated to boron, giving dioxazaborocines. X-ray crystal structures of two analogues are reported. These compounds are capable of releasing borate ions and are therefore potentially biologically active.

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