112655-19-3

Usage

Uses

Used in Organic Synthesis:
IMIDAZOLE-2-CARBOXALDEHYDE DIMETHYL ACETAL, 98+% is used as a reagent in chemical reactions for organic synthesis. Its high purity level makes it suitable for various significant applications in this field.
Used in Pharmaceutical Industry:
IMIDAZOLE-2-CARBOXALDEHYDE DIMETHYL ACETAL, 98+% is used as an intermediate in the synthesis of various pharmaceutical compounds. Its unique structure and reactivity contribute to the development of new drugs and therapeutic agents.
Used in Chemical Research:
IMIDAZOLE-2-CARBOXALDEHYDE DIMETHYL ACETAL, 98+% is used as a research compound in various chemical studies. Its properties and reactivity are investigated to understand its potential applications and to develop new synthetic methods and techniques.

InChI:InChI=1/C6H10N2O2/c1-9-6(10-2)5-7-3-4-8-5/h3-4,6H,1-2H3,(H,7,8)

Upstream product

• 67-56-1 methanol 
• 10111-08-7 2-imidazolecarbaldehyde 
• 131543-46-9 Glyoxal 
• 51673-84-8 dimethoxyacetaldehyde 

Relevant academic research and scientific papers

Quaternary Salts of 2-imidazole. 5. Structure-Activity Relationships for Side-Chain Nitro-, Sulfone-, Amino-, and Aminosulfonyl-Substituted Analogues for Therapy against Anticholinesterase Intoxication

Several quaternary imidazolium oxime derivatives incorporating side chains bearing nitro, sulfone, amino, and aminosulfonyl substituents were prepared and evaluated as treatment therapeutics for anti-AChE intoxication.In vivo test results in the mouse rev

Preparation process for 2 formyl imidazole acetals

Preparation process for a product of formula (I): STR1 in which R1 and R2, either are identical and represent a C1 -C4 alkyl radical, or form together a group of formula (II): in which R3, R4, R5 and R6, identical or different, represent a hydrogen atom or a C1 -C4 alkyl radical, and n represents 0 or 1, in which an aqueous mixture of glyoxal and an ethanal of formula (III): STR2 in which R1 and R2 have the meaning given above, is reacted with ammonia.