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α,4-Diacetoxy-3-methoxyacetophenone is a chemical compound with the molecular formula C12H14O5. It is an aromatic ketone derivative, featuring a phenyl ring with a ketone group (-COCH3) at the 1-position, a methoxy group (-OCH3) at the 3-position, and two acetoxy groups (-OOCCH3) at the α (1) and 4 positions. α,4-diacetoxy-3-methoxyacetophenone is known for its potential applications in the synthesis of various pharmaceuticals and agrochemicals, particularly as an intermediate in the production of certain pesticides. It is also used in the preparation of dyes and other specialty chemicals. Due to its reactivity and functional groups, α,4-diacetoxy-3-methoxyacetophenone is a valuable building block in organic chemistry, allowing for further modification and the creation of a wide range of compounds.

19767-93-2

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19767-93-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 19767-93-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,9,7,6 and 7 respectively; the second part has 2 digits, 9 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 19767-93:
(7*1)+(6*9)+(5*7)+(4*6)+(3*7)+(2*9)+(1*3)=162
162 % 10 = 2
So 19767-93-2 is a valid CAS Registry Number.

19767-93-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name α,4-diacetoxy-3-methoxyacetophenone

1.2 Other means of identification

Product number -
Other names 2-Acetoxy-1-(4-acetoxy-3-methoxy-phenyl)-aethanon

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:19767-93-2 SDS

19767-93-2Relevant academic research and scientific papers

Facile synthesis of glycol metabolites of phenethylamine drugs

Holshouser,Kolb

, p. 619 - 621 (2007/10/02)

High yields of potential glycol metabolites of p-synephrine, epinephrine, octopamine, and normacromerine can be obtained from the readily available monosubstituted and disubstituted acetophenones. The general procedure involves alpha-bromination followed by displacement with acetate ion and reduction with lithium aluminum hydride. Yields ranged from 46 to 91%. Furthermore, the procedure minimizes some problems inherent in aromatic glycol synthesis which include dimerization and pinacol-pinacolone rearrangement.

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