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2,4-bis(benzyloxy)-5-bromobenzaldehyde is a chemical compound characterized by the molecular formula C21H19BrO3. It is a yellow solid with a molecular weight of 391.28 g/mol. 2,4-bis(benzyloxy)-5-bromobenzaldehyde is known for its unique structure and reactivity, which makes it a valuable building block in organic synthesis and chemical research for the creation of complex molecules.

898538-49-3

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898538-49-3 Usage

Uses

Used in Organic Synthesis:
2,4-bis(benzyloxy)-5-bromobenzaldehyde is used as a building block in organic synthesis for the creation of various complex molecules. Its unique structure and reactivity contribute to the formation of a wide range of chemical compounds.
Used in Chemical Research:
In the field of chemical research, 2,4-bis(benzyloxy)-5-bromobenzaldehyde serves as an important intermediate, facilitating the development and understanding of new chemical reactions and processes.
Used in Pharmaceutical Development:
2,4-bis(benzyloxy)-5-bromobenzaldehyde is utilized in the development of pharmaceuticals, where its properties can be harnessed to create new drugs with potential therapeutic applications.
Used in Agrochemical Development:
2,4-bis(benzyloxy)-5-bromobenzaldehyde also finds application in the development of agrochemicals, where it can be used to create new products for agricultural use, such as pesticides or herbicides.
Used in Industrial Product Development:
2,4-bis(benzyloxy)-5-bromobenzaldehyde is employed in the development of various industrial products, leveraging its unique properties to enhance the performance or functionality of these products.

Check Digit Verification of cas no

The CAS Registry Mumber 898538-49-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,9,8,5,3 and 8 respectively; the second part has 2 digits, 4 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 898538-49:
(8*8)+(7*9)+(6*8)+(5*5)+(4*3)+(3*8)+(2*4)+(1*9)=253
253 % 10 = 3
So 898538-49-3 is a valid CAS Registry Number.

898538-49-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 2,4-bis-benzyloxy-5-bromo-benzaldehyde

1.2 Other means of identification

Product number -
Other names 5-bromo-2,4-(dibenzyloxy)benzaldehyde

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:898538-49-3 SDS

898538-49-3Relevant academic research and scientific papers

TRIAZOLE COMPOUNDS THAT MODULATE HSP90 ACTIVITY

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, (2008/06/13)

The present invention relates to substituted triazole compounds and compositions comprising substituted triazole compounds. The invention further relates to methods of inhibiting the activity of Hsp90 in a subject in need thereof and methods for preventing or treating hyperproliferative disorders, such as cancer, in a subject in need thereof comprising administering to the subject a substituted triazole compound of the invention, or a composition comprising such a compound.

NOVEL HSP90 INHIBITOR

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Page/Page column 41, (2010/11/28)

Disclosed is a triazole derivative represented by the general formula (1) below or a pharmacologically acceptable salt thereof. Also disclosed are a prodrug of such a triazole derivative and an HSP90 inhibitor containing any one of them as an active constituent. (1) (In the formula, X represents a halogen atom, an optionally substituted alkyl group, an optionally substituted alkenyl group or the like; Y represents a mercapto group, a hydroxyl group, an optionally substituted sulfonyl group, an optionally substituted amino group or the like; and R represents an optionally substituted aryl or amino group or the like.)

1-THIO-D-GLUCITOL DERIVATIVES

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Page/Page column 42-43, (2010/11/28)

The present invention provides a 1-thio-D-glucitol compound of the following formula, which shows the action of inhibiting the activity of SGLT2, a pharmaceutically acceptable salt of the compound, or a hydrate of the compound or the salt; and a pharmaceu

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