1652-96-6

Basic information

• Product Name: 2-Dodecene
• Synonyms: 2-Dodecene
• CAS NO: 1652-96-6
• Molecular Formula: C₁₂H₂₄
• Molecular Weight: 168.32
• Mol File: 1652-96-6.mol
• Article Data: 18

Chemical Properties

• Melting Point: -38.4°C (estimate)
• Boiling Point: 207.3°C (estimate)
• Flash Point: 78.8°C
• Appearance: /
• Density: 0.7761 (estimate)
• Vapor Pressure: 0.209mmHg at 25°C
• Refractive Index: 1.4287 (estimate)
• CAS DataBase Reference: 2-Dodecene(CAS DataBase Reference)
• NIST Chemistry Reference: 2-Dodecene(1652-96-6)
• EPA Substance Registry System: 2-Dodecene(1652-96-6)

Safety Data

• Hazardous Substances Data: 1652-96-6(Hazardous Substances Data)

Usage

InChI:InChI=1/C12H24/c1-3-5-7-9-11-12-10-8-6-4-2/h3,5H,4,6-12H2,1-2H3

Upstream product

• 2350-11-0 2-chlorododecane 
• 35021-68-2 dodecyloxybenzene 
• 1623-99-0 phenyl sodium 
• 3507-99-1 silver⁽¹⁺⁾ stearate 
• 71-43-2 benzene 
• 112-41-4 1-dodecene 
• 114114-75-9 Methanesulfonic acid 1-methyl-undecyl ester 
• 201230-82-2 carbon monoxide 
• 143-15-7 1-dodecylbromide 
• 68453-80-5 2-iodododecane 
• 69944-94-1 1,2-dodecadiene 
• 765-03-7 1-dodecyne 
• 13187-99-0 2-bromododecane 
• 100-58-3 phenylmagnesium bromide 

Relevant articles and documents

OXIDATION OF OLEFINS BY OXYGEN WITH A MIXED PALLADIUM/SILVER NITRITE CATALYST IN ALCOHOLS.

Selective oxidation of a terminal olefin by a mixed catalytic system comprising Pd(dba)2 and silver nitrite gives a methyl ketone.A WACKER type mechanism is proposed, in which organic nitrites derives from the alcoholic solvent used are involved.

Mild olefin formationviabio-inspired vitamin B12photocatalysis

Dehydrohalogenation, or elimination of hydrogen-halide equivalents, remains one of the simplest methods for the installation of the biologically-important olefin functionality. However, this transformation often requires harsh, strongly-basic conditions, rare noble metals, or both, limiting its applicability in the synthesis of complex molecules. Nature has pursued a complementary approach in the novel vitamin B12-dependent photoreceptor CarH, where photolysis of a cobalt-carbon bond leads to selective olefin formation under mild, physiologically-relevant conditions. Herein we report a light-driven B12-based catalytic system that leverages this reactivity to convert alkyl electrophiles to olefins under incredibly mild conditions using only earth abundant elements. Further, this process exhibits a high level of regioselectivity, producing terminal olefins in moderate to excellent yield and exceptional selectivity. Finally, we are able to access a hitherto-unknown transformation, remote elimination, using two cobalt catalysts in tandem to produce subterminal olefins with excellent regioselectivity. Together, we show vitamin B12to be a powerful platform for developing mild olefin-forming reactions.

Cobalt-Catalyzed Intermolecular Hydrofunctionalization of Alkenes: Evidence for a Bimetallic Pathway

A functional group tolerant cobalt-catalyzed method for the intermolecular hydrofunctionalization of alkenes with oxygen- and nitrogen-based nucleophiles is reported. This protocol features a strategic use of hypervalent iodine(III) reagents that enables a mechanistic shift from conventional cobalt-hydride catalysis. Key evidence was found supporting a unique bimetallic-mediated rate-limiting step involving two distinct cobalt(III) species, from which a new carbon-heteroatom bond is formed.