Welcome to LookChem.com Sign In|Join Free
  • or
4-(4-N-PROPYLPHENYL)BENZALDEHYDE, a chemical compound with the molecular formula C16H18O, is a benzaldehyde derivative characterized by the attachment of a propyl group to the fourth position of the phenyl ring. 4-(4-N-PROPYLPHENYL)BENZALDEHYDE is recognized for its potential antiseptic and antibacterial properties, as well as its antioxidant and anti-inflammatory activities, positioning it as a promising candidate for diverse medical and industrial applications.

93972-05-5

Post Buying Request

93972-05-5 Suppliers

Recommended suppliers

  • Product
  • FOB Price
  • Min.Order
  • Supply Ability
  • Supplier
  • Contact Supplier

93972-05-5 Usage

Uses

Used in Pharmaceutical Industry:
4-(4-N-PROPYLPHENYL)BENZALDEHYDE is used as an intermediate in the synthesis of various pharmaceuticals for its potential antiseptic and antibacterial properties. Its antioxidant and anti-inflammatory activities also contribute to its value in developing new medications.
Used in Agrochemical Industry:
In the agrochemical sector, 4-(4-N-PROPYLPHENYL)BENZALDEHYDE is utilized as a component in the production of agrochemicals, leveraging its antiseptic and antibacterial properties to enhance crop protection and management.
Used in Flavoring Agents:
4-(4-N-PROPYLPHENYL)BENZALDEHYDE is employed as a flavoring agent in the food and beverage industry, capitalizing on its aromatic properties to impart unique flavors and scents to products.
Used in Antioxidant and Anti-Inflammatory Applications:
4-(4-N-PROPYLPHENYL)BENZALDEHYDE is used as an antioxidant and anti-inflammatory agent in various formulations, including cosmetics and healthcare products, to provide protective and soothing effects on the skin and other biological systems.

Check Digit Verification of cas no

The CAS Registry Mumber 93972-05-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,3,9,7 and 2 respectively; the second part has 2 digits, 0 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 93972-05:
(7*9)+(6*3)+(5*9)+(4*7)+(3*2)+(2*0)+(1*5)=165
165 % 10 = 5
So 93972-05-5 is a valid CAS Registry Number.

93972-05-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-(4-n-Propylphenyl)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:93972-05-5 SDS

93972-05-5Downstream Products

93972-05-5Relevant academic research and scientific papers

Parallel synthesis of aldehydes and ketone facilitated by a new solid- phase Weinreb amide

Salvino, Joseph M.,Mervic, Miljenko,Mason, Helen J.,Kiesow, Terence,Teager, David,Airey, John,Labaudiniere, Richard

, p. 1823 - 1830 (2007/10/03)

This paper describes a novel supported Weinreb amide resin that facilitates parallel synthesis of aldehydes and ketones on a scale useful for chemical library synthesis. This new resin makes it possible to produce custom aldehydes and ketones from a wide range of carboxylic acids, including N-BOC-amino acids. A variety of commercially unavailable aldehydes are easily synthesized in parallel and obtained in high purity via a simple filtration workup, thus facilitating parallel synthesis of lead optimization libraries that typically require custom synthesis of aldehyde intermediates for development of structure-activity relationships. To demonstrate the utility of this method, we synthesized a small library based on a supported Horner- Emmons reagent. This is the first time it has been shown that aldehydes generated via a supported Weinreb amide could be used directly as reagents in chemical library synthesis employing moisture-sensitive reactions. The analogous solution reaction is not suited for parallel synthesis because of the laborious extractive workup procedure necessary and, at times, the instability of these reactive intermediates.

Post a RFQ

Enter 15 to 2000 letters.Word count: 0 letters

Attach files(File Format: Jpeg, Jpg, Gif, Png, PDF, PPT, Zip, Rar,Word or Excel Maximum File Size: 3MB)

1 Customer Service

What can I do for you?
Get Best Price

Get Best Price for 93972-05-5