22123-53-1

Basic information

• Product Name: 2,2-Dimethylpropylidenemalononitrile
• Synonyms: (2,2-Dimethylpropylidene)malononitrile;2-(2,2-Dimethylpropylidene)propanedinitrile;2,2-Dimethylpropylidenemalononitrile;3,3-Dimethyl-1-butene-1,1-dicarbonitrile
• CAS NO: 22123-53-1
• Molecular Formula: C₈H₁₀N₂
• Molecular Weight: 0
• Mol File: 22123-53-1.mol
• Article Data: 11

Chemical Properties

• Appearance: /
• CAS DataBase Reference: 2,2-Dimethylpropylidenemalononitrile(CAS DataBase Reference)
• NIST Chemistry Reference: 2,2-Dimethylpropylidenemalononitrile(22123-53-1)
• EPA Substance Registry System: 2,2-Dimethylpropylidenemalononitrile(22123-53-1)

Safety Data

• Hazardous Substances Data: 22123-53-1(Hazardous Substances Data)

Upstream product

• 630-19-3 pivalaldehyde 
• 109-77-3 malononitrile 

Downstream Products

• 10413-34-0 2-amino-3-cyano-4-tert-butyl-thiophene 

Relevant articles and documents

Synthesis of hybrid perillyl-4H-pyrans. Cytotoxicity evaluation against hepatocellular carcinoma HepG2/C3A cell line

A series of 15 new hybrid perillyl-4H-pyrans compounds was straightforwardly synthesized by a strategy combining the multicomponent reaction and the copper-catalyzed alkyne-azide cycloaddition (CuAAC). The 2-amino-4H-pyrans-3-carbonitrile containing the a

Utilization of hexagonal boron nitride as a solid acid–base bifunctional catalyst

This work explores the use of hexagonal boron nitride (h-BN), a graphite-like compound, as a novel catalyst with base and acid functionalities. For use as a solid catalyst, the layered structure of h-BN was disrupted by ball-milling, exposing boron and ni

Hierarchical high-silica zeolites as superior base catalysts

For more than four decades, the design of zeolite base catalysts has relied on the application of aluminium-rich frameworks exchanged with alkali metal cations (preferably Cs+). However, moderate activity associated with access and diffusion limitations, and high manufacturing costs associated with high caesium content (typically over 30%) have hampered their industrial implementation so far. Herein, we have discovered that high-silica USY zeolites outperform their Al-rich counterparts in a variety of base-catalysed reactions of relevance in the fine chemical industry, as well as in the upgrading of biofuels. The benefits of this class of materials are amplified upon the alleviation of diffusion constraints through the introduction of a network of intracrystalline mesopores by post-synthetic modification. For example, the resulting cation-free hierarchical USY provides an up to 30-fold Knoevenagel condensation activity compared to the benchmark Cs-X, and similar observations were made upon application in liquid-phase (nitro)aldol reactions. Moreover, in the gas-phase aldol condensation of propanal, high-silica zeolites provide superior activity, selectivity, and lifetime compared to caesium-containing zeolites and even a strong solid base such as MgO. We decouple the complex interplay between mesoporosity and intrinsic zeolitic properties such as crystallinity, and quantify the increase in catalyst effectiveness upon hierarchical structuring as a function of reactant size. The obtained results are a major step to resolve the drawbacks of zeolites catalysis and thereby revitalise their potential for industrial application.