134839-87-5

Basic information

• Product Name: D3-METHYL BENZOYLFORMATE
• Synonyms: METHYL-D3 PHENYLGLYOXYLATE;D3-METHYL BENZOYLFORMATE
• CAS NO: 134839-87-5
• Molecular Formula: C₉H₈O₃
• Molecular Weight: 167.18
• Mol File: 134839-87-5.mol
• Article Data: 3

Chemical Properties

• Appearance: /
• CAS DataBase Reference: D3-METHYL BENZOYLFORMATE(CAS DataBase Reference)
• NIST Chemistry Reference: D3-METHYL BENZOYLFORMATE(134839-87-5)
• EPA Substance Registry System: D3-METHYL BENZOYLFORMATE(134839-87-5)

Safety Data

• Hazardous Substances Data: 134839-87-5(Hazardous Substances Data)

Usage

General Description

D3-Methyl benzoylformate is a chemical compound that belongs to the class of organic compounds known as benzoylformates. It is a white, crystalline substance that is commonly used as a flavoring agent in the food industry. It has a sweet, fruity aroma and is often used in the production of perfumes and other fragrances. D3-Methyl benzoylformate is also utilized in the synthesis of pharmaceuticals and other organic compounds. Due to its potential for skin and eye irritation, it should be handled and used with care.

Upstream product

• 811-98-3 d⁽⁴⁾-methanol 
• 62977-82-6 benzyl oxo(phenyl)acetate 
• 1603-79-8 phenylglyoxylic acid ethyl ester 
• 13665-04-8 2,2-dibromoacetophenone 

Downstream Products

• 134839-77-3 1-d3-Methyl-4-methyl 2-phenylfumarate 
• 134839-78-4 1-d3-Methyl-4-methyl 2-phenylmaleate 
• 134839-66-0 C₁₂H₁₁⁽²⁾H₃O₄ 

Relevant articles and documents

Synthesis and Properties of 1-Acyl Triazenes

1-Acyl triazenes can be prepared by acid-catalyzed hydration, gold/iodine-catalyzed oxidation, or oxyhalogenation of 1-alkynyl triazenes. Crystallographic analyses reveal a pronounced effect of the acyl group on the electronic structure of the triazene fu

An efficient and practical synthesis of aryl and hetaryl α-keto esters

A general and highly efficient method was developed for the synthesis of -keto esters by oxidative esterification of 2,2-dibromo-1-(het)arylethanones by sequential treatment with dimethyl sulfoxide and an alkanol. The versatility of the reaction was established by synthesizing a range of -keto esters by treatment of 2,2-dibromoethanones, derived from aryl or hetaryl ketones, with di-methyl sulfoxide and a cyclic or acyclic primary or secondary alcohol. The mechanism of the reaction was established by means of a detailed study. Georg Thieme Verlag Stuttgart · New York.