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3-[(2,6-DICHLOROBENZYL)OXY]BENZALDEHYDE is a chemical compound characterized by the molecular formula C14H10Cl2O2. It features an aldehyde group attached to a benzene ring, with a chlorobenzyl moiety connected to an oxygen atom. Known for its aromatic properties and reactivity, 3-[(2,6-DICHLOROBENZYL)OXY]BENZALDEHYDE serves as a versatile building block in the synthesis of pharmaceuticals, dyes, and fragrances. Additionally, it functions as a reagent in organic chemistry and holds promise in medicinal chemistry for the development of novel drug precursors. However, due to potential health and safety risks, careful handling is essential when working with 3-[(2,6-DICHLOROBENZYL)OXY]BENZALDEHYDE.

328062-72-2

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328062-72-2 Usage

Uses

Used in Pharmaceutical Industry:
3-[(2,6-DICHLOROBENZYL)OXY]BENZALDEHYDE is used as a key intermediate in the synthesis of various pharmaceuticals for its aromatic properties and reactivity, contributing to the development of new drugs with potential therapeutic applications.
Used in Dye and Fragrance Industry:
In the dye and fragrance industry, 3-[(2,6-DICHLOROBENZYL)OXY]BENZALDEHYDE is utilized as a precursor for creating aromatic compounds that impart color and scent to products, capitalizing on its chemical structure to enhance sensory attributes.
Used in Organic Chemistry Research:
3-[(2,6-DICHLOROBENZYL)OXY]BENZALDEHYDE serves as a reagent in organic chemistry reactions, facilitating the synthesis of complex organic molecules and aiding in the advancement of chemical research and development.
Used in Medicinal Chemistry:
3-[(2,6-DICHLOROBENZYL)OXY]BENZALDEHYDE is employed as a precursor in medicinal chemistry for the development of innovative drug candidates, leveraging its chemical properties to explore new therapeutic possibilities.

Check Digit Verification of cas no

The CAS Registry Mumber 328062-72-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,2,8,0,6 and 2 respectively; the second part has 2 digits, 7 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 328062-72:
(8*3)+(7*2)+(6*8)+(5*0)+(4*6)+(3*2)+(2*7)+(1*2)=132
132 % 10 = 2
So 328062-72-2 is a valid CAS Registry Number.
InChI:InChI=1/C14H10Cl2O2/c15-13-5-2-6-14(16)12(13)9-18-11-4-1-3-10(7-11)8-17/h1-8H,9H2

328062-72-2SDS

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 3-[(2,6-dichlorophenyl)methoxy]benzaldehyde

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:328062-72-2 SDS

328062-72-2Downstream Products

328062-72-2Relevant academic research and scientific papers

ALKOXY COMPOUNDS FOR DISEASE TREATMENT

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Page/Page column 228, (2009/05/29)

The present invention relates generally to compositions and methods for treating neurodegenerative diseases and disorders, particularly ophthalmic diseases and disorders. Provided herein are alkoxyl derivative compounds and pharmaceutical compositions comprising these compounds. The subject compositions are useful for treating and preventing ophthalmic diseases and disorders, including age-related macular degeneration (AMD) and Stargardt's Disease.

Fatty acid synthase inhibitors

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, (2008/06/13)

This invention relates to the use of compounds as inhibitors of the fatty acid synthase FabH.

Fatty acid synthase inhibitors

-

, (2008/06/13)

This invention relates to the use of compounds as inhibitors of the fatty acid synthase FabH.

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