134283-49-1

Basic information

• Product Name: (E)-4-hydroxy-3-methoxybenzaldehyde oxime
• Synonyms: (E)-4-hydroxy-3-methoxybenzaldehyde oxime
• CAS NO: 134283-49-1
• Molecular Weight: 167.164
• Mol File: 134283-49-1.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: (E)-4-hydroxy-3-methoxybenzaldehyde oxime(CAS DataBase Reference)
• NIST Chemistry Reference: (E)-4-hydroxy-3-methoxybenzaldehyde oxime(134283-49-1)
• EPA Substance Registry System: (E)-4-hydroxy-3-methoxybenzaldehyde oxime(134283-49-1)

Safety Data

• Hazardous Substances Data: 134283-49-1(Hazardous Substances Data)

Usage

General Description

(E)-4-hydroxy-3-methoxybenzaldehyde oxime, also known as vanillin oxime, is a chemical compound with the molecular formula C8H9NO2. It is the oxime derivative of vanillin, which is a well-known flavoring agent commonly found in vanilla beans. Vanillin oxime has been studied for its potential biological and pharmacological properties, including its antioxidant and anti-inflammatory effects. It has also been investigated for its potential use in the development of pharmaceuticals and food additives. Additionally, vanillin oxime has been studied for its potential role in the synthesis of various organic compounds, making it a versatile and valuable chemical in a wide range of scientific and industrial applications.

Upstream product

• 121-33-5 vanillin 

Relevant articles and documents

Preparation method O - alkyl substituted hydroxylamine salt

The invention relates to a preparation method of N - alkyl substituted hydroxylamine salt, and belongs to fine chemical engineering. Pesticide or bulk pharmaceutical chemicals technical field. The present invention reacts with the N - alkyl of the oxime with an inorganic salt of hydroxylamine to give N - alkyl-substituted hydroxylamine salt and oxime. The invention provides an efficient and environment-friendly method for preparing N - alkyl substituted hydroxylamine salt, and simultaneously, an N - alkyl substituted hydroxylamine salt is prepared, and the oxime can be re-prepared to form N - alkylate of oxime so as to realize the material circulation. No equivalent acid is used in the reaction process. Alkali neutralization, avoided the current method to use a large amount of acid, alkali and produce inorganic salt solid waste shortcoming, environmental protection more. The preparation method is mild in reaction condition, and the defects of high pollution and high energy consumption of the traditional process are overcome. In-flight R1 , R2 What is R is as claimed in the claims and the description.

A mild procedure for rapid and selective deprotection of aryl acetates using natural kaolinitic clay as a reusable catalyst

A variety of aryl acetates are selectively cleaved to the corresponding phenols using natural kaolinitic clay in methanol under mild conditions (25°C).