592479-02-2

Usage

Uses

Used in Organic Synthesis:
1-(2,2-DiMethoxy-ethyl)-2-isocyano-benzene is used as a reactant in organic synthesis for its reactivity and versatility in forming a variety of organic compounds.
Used in Pharmaceutical Production:
DIMB is utilized as a key component in the production of pharmaceuticals, contributing to the development of new medications and therapeutic agents.
Used in Chemical Research:
As a reactive isocyanobenzene derivative, 1-(2,2-DiMethoxy-ethyl)-2-isocyano-benzene is also used in chemical research to study the properties and reactions of isocyanate compounds, furthering the understanding of their applications in various industries.
Used in the Production of Other Organic Compounds:
DIMB serves as a starting material or intermediate in the synthesis of other organic compounds, highlighting its importance in the broader scope of organic chemistry.
Safety Precautions:
Given its toxicity, 1-(2,2-DiMethoxy-ethyl)-2-isocyano-benzene requires proper safety measures during handling, including the use of personal protective equipment and working in well-ventilated areas to minimize exposure risks.

Upstream product

• 592478-96-1 N-[2-(2,2-dimethoxyethyl)phenyl]formamide 
• 150760-45-5 2-(2,2-dimethoxyethyl)-benzeneamine 
• 79844-33-0 2-(2-nitrophenyl)acetaldehyde dimethyl acetal 
• 88-72-2 1-methyl-2-nitrobenzene 
• 20973-67-5 N,N-dimethyl-2-(2-nitrophenyl)ethenylamine 
• 32989-69-8 trans-2-nitro-β-pyrrolidinostyrene 

Downstream Products

• 938074-92-1 C₁₈H₂₆N₂O₅ 
• 938074-90-9 C₁₉H₂₈N₂O₄ 
• 938074-94-3 C₂₁H₃₁N₃O₆ 
• 938074-96-5 C₁₆H₂₁N₂O₄Br 
• 938074-98-7 C₁₇H₂₄N₂O₄ 
• 938074-86-3 C₁₆H₂₂N₂O₄ 
• 951024-67-2 C₂₄H₃₀N₂O₅ 
• 951024-74-1 C₂₈H₃₆N₂O₇ 
• 1017278-26-0 4-(benzyloxy)-2-((tert-butyl(dimethyl)silyloxy)methyl)-N-(2-(2,2-dimethoxyethyl)phenyl)-5-oxopyrrolidine-2-carboxamide 
• 1148116-48-6 C₁₅H₁₈Cl₃NO₅ 
• 1148116-45-3 C₁₆H₂₁N₅O₅ 

Relevant academic research and scientific papers

COMPOUNDS USEFUL IN HIV THERAPY

The invention relates to compounds of Formula (I), (Ia), (Ib), (II) or (III), salts thereof, pharmaceutical compositions thereof, as well as therapeutic methods of treatment and prevention.

TFA-catalysed tandem double cyclisation: A one-pot, metal-free routes for novel indolo-imidazo[1,2-a]pyridine derivatives

A transition-metal free, one-pot tandem synthetic routes for novel indole and imidazo[1,2-a]pyridine derivative hybrids have been established. An efficient three-component reaction was designed with incorporation of two sequential Groebke–Blackburn–Bienay

Application of the Cleavable Isocyanide in Efficient Approach to Pyroglutamic Acid Analogues with Potential Biological Activity

Two efficient procedures have been developed for the synthesis of pyroglutamic acid analogues 28, 29, and 34. According to the first method the Ugi (4C3C) reaction is followed by a post-transformation reaction, and the second method involves the Michael a

New entry to convertible isocyanides for the Ugi reaction and its application to the stereocontrolled formal total synthesis of the proteasome inhibitor omuralide

The development of a new convertible isocyanide, indole-isocyanide, for ready access to pyroglutamic acids culminated in the formal total synthesis of the proteasome inhibitor omuralide featuring a stereocontrolled Ugi reaction. Indole-isocyanide was name

Synthesis of 3-methoxyquinolines via cyclization of 1-isocyano-2-(2-lithio-2-methoxyethenyl)benzenes

2-(2-Isocyanophenyl)acetaldehyde dimethyl acetals were treated with excess LDA to generate 1-isocyano-2-(2-lithio-2-methoxyethenyl)benzenes, which cyclized intramolecularly to afford 3-methoxyquinolines in good to excellent yields.