Welcome to LookChem.com Sign In|Join Free

CAS

  • or

151340-06-6

Post Buying Request

151340-06-6 Suppliers

Recommended suppliersmore

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

151340-06-6 Usage

Description

1-(2-chloro-4-hydroxy-3-methoxyphenyl)ethanone, also known as acetophenone-2-chloro-4-hydroxy-3-methylanisole, is a chemical compound with the molecular formula C9H9ClO3. It is a derivative of acetophenone, featuring a chloro, hydroxy, and methoxy group attached to the phenyl ring. 1-(2-chloro-4-hydroxy-3-methoxyphenyl)ethanone is recognized for its aromatic properties and is commonly utilized in the synthesis of pharmaceuticals and fragrances. Furthermore, it has been investigated for its potential antioxidant and antibacterial properties, which makes it a compound of interest for both medicinal and industrial applications. However, due to its potentially hazardous nature, it is crucial to exercise caution when handling and storing this chemical.

Uses

Used in Pharmaceutical Synthesis:
1-(2-chloro-4-hydroxy-3-methoxyphenyl)ethanone is used as an intermediate in the pharmaceutical industry for the synthesis of various drugs. Its unique chemical structure allows for the creation of a wide range of medicinal compounds, contributing to the development of novel treatments for different health conditions.
Used in Fragrance Production:
In the fragrance industry, 1-(2-chloro-4-hydroxy-3-methoxyphenyl)ethanone is used as a key component in the creation of various aromatic compounds. Its distinct scent profile makes it a valuable addition to the formulation of perfumes, colognes, and other scented products.
Used in Antioxidant Applications:
1-(2-chloro-4-hydroxy-3-methoxyphenyl)ethanone is used as an antioxidant in the chemical and industrial sectors. Its potential antioxidant properties make it a candidate for use in stabilizing products and materials that are prone to oxidative degradation, thereby extending their shelf life and maintaining their quality.
Used in Antibacterial Applications:
1-(2-chloro-4-hydroxy-3-methoxyphenyl)ethanone is also being studied for its potential antibacterial properties. If proven effective, 1-(2-chloro-4-hydroxy-3-methoxyphenyl)ethanone could be used in the development of new antibacterial agents, contributing to the fight against antibiotic-resistant bacteria and improving public health.

Check Digit Verification of cas no

The CAS Registry Mumber 151340-06-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,5,1,3,4 and 0 respectively; the second part has 2 digits, 0 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 151340-06:
(8*1)+(7*5)+(6*1)+(5*3)+(4*4)+(3*0)+(2*0)+(1*6)=86
86 % 10 = 6
So 151340-06-6 is a valid CAS Registry Number.

151340-06-6SDS

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 1-(2-chloro-4-hydroxy-3-methoxyphenyl)ethanone

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:151340-06-6 SDS

151340-06-6Downstream Products

151340-06-6Relevant articles and documents

Preparation and properties of chlorinated syringic acids, acetosyringones, acetoguaiacones and methoxy-p-hydroquinones components of pulp bleaching effluents

Smith,Wearne,Wallis

, p. 69 - 80 (2007/10/03)

A range of chlorinated phenols which serve as standards for compounds occurring in effluents from the bleaching of wood pulps with chlorine-containing reagents has been prepared. The chlorinated phenols include chlorosyringic acids, chloroacetosyringones, chloroacetoguaiacones, 5-chloro-2-methoxy-p-hydroquinone and chloro-2,6-dimethoxy-p-hydroquinones. With the exception of the ring-chlorinated acetoguaiacones which were prepared by reaction of chlorovanillin acetates with diazomethane, the compounds were obtained by direct chlorination of appropriate phenols or their acetates. Gas chromatographic and mass spectrometric data for the acetylated phenols are given.

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

What can I do for you?
Get Best Price

Get Best Price for 151340-06-6