2510-03-4

Basic information

• Product Name: Propanedinitrile, (3,4-dihydro-1(2H)-naphthalenylidene)-
• CAS NO: 2510-03-4
• Molecular Formula: C13H10N2
• Molecular Weight: 194.236
• Mol File: 2510-03-4.mol
• Article Data: 25

Chemical Properties

• CAS DataBase Reference: Propanedinitrile, (3,4-dihydro-1(2H)-naphthalenylidene)-(CAS DataBase Reference)
• NIST Chemistry Reference: Propanedinitrile, (3,4-dihydro-1(2H)-naphthalenylidene)-(2510-03-4)
• EPA Substance Registry System: Propanedinitrile, (3,4-dihydro-1(2H)-naphthalenylidene)-(2510-03-4)

Safety Data

• Hazardous Substances Data: 2510-03-4(Hazardous Substances Data)

Upstream product

• 529-34-0 3,4-dihydronaphthalene-1(2H)-one 
• 109-77-3 malononitrile 
• 1846-17-9 2-(1,2,3,4-tetrahydronaphthalen-1-yl)malononitrile 

Downstream Products

• 1203611-32-8 C₂₅H₂₇N₃O₂S 
• 1203611-51-1 C₂₅H₂₇N₃O₂S 
• 1203611-60-2 C₂₅H₂₇N₃O₂S 
• 1203611-57-7 C₂₅H₂₇N₃O₂S 

Relevant articles and documents

Asymmetric organocatalytic vinylogous Michael addition triggered triple-cascade reactions of 2-hydroxycinnamaldehydes and vinylogous nucleophiles: construction of benzofused oxabicyclo[3.3.1]nonane scaffolds

An organocatalytic vinylogous Michael addition triggered triple-cascade reaction has been developed. 2-Hydroxycinnamaldehydes worked under iminium activation with either acyclic or cyclic ketone-derived α,α-dicyanoalkenes, yielding the benzofused oxabicyclo[3.3.1]nonanes bearing one quaternary stereocenter with excellent stereoselectivities.

"on Water" Direct Catalytic Vinylogous Aldol Reaction of Silyl Glyoxylates

The unique reactivity of water in the direct catalytic vinylogous aldol reaction of silyl glyoxylates is reported. With the hydrogen-bonding networks from water, the unfavorable homogeneous reactions in organic solvents were severely suppressed, and the "

Synthesis of 2-cyanoacrylamides through Pd-catalyzed monohydration of methylenemalononitriles

A straightforward and efficient method has been developed for the synthesis of 2-cyanoacrylamide from 2-methylenemalononitriles through monohydration. A series of methylenemalononitriles underwent the reaction under mild and simple reaction conditions wit