41446-54-2

Basic information

• Product Name: (Z)-4-Tridecene
• Synonyms: (Z)-4-Tridecene
• CAS NO: 41446-54-2
• Molecular Formula: C₁₃H₂₆
• Molecular Weight: 182.34554
• Mol File: 41446-54-2.mol
• Article Data: 12

Chemical Properties

• Boiling Point: 232.3°C at 760 mmHg
• Flash Point: 87.2°C
• Appearance: /
• Density: 0.77g/cm³
• Vapor Pressure: 0.0903mmHg at 25°C
• Refractive Index: 1.439
• CAS DataBase Reference: (Z)-4-Tridecene(CAS DataBase Reference)
• NIST Chemistry Reference: (Z)-4-Tridecene(41446-54-2)
• EPA Substance Registry System: (Z)-4-Tridecene(41446-54-2)

Safety Data

• Hazardous Substances Data: 41446-54-2(Hazardous Substances Data)

Usage

Synthesis Reference(s)

Synthetic Communications, 12, p. 107, 1982 DOI: 10.1080/00397918208063662

InChI:InChI=1/C13H26/c1-3-5-7-9-11-13-12-10-8-6-4-2/h7,9H,3-6,8,10-13H2,1-2H3/b9-7-

Upstream product

• 124-19-6 nonan-1-al 
• 1779-51-7 n-butyl(triphenyl)phosphonium bromide 
• 627-19-0 1-Pentyne 
• 111-66-0 oct-1-ene 
• 629-50-5 Tridecane 
• 35329-42-1 undec-1-en-3-ol 
• 925-90-6 ethylmagnesium bromide 
• 694-54-2 tetrahydro-2H-2-pyranol 
• 1292288-89-1 (Z)-9-tridecen-5-ol 
• 1292288-90-4 O-phenyl O-(Z)-9-tridecen-5-yl thionocarbonate 
• 64275-75-8 (Z)-non-5-en-1-ol 
• 2277-17-0 (Z)-5-nonenal 
• 872-05-9 1-Decene 
• 7642-15-1 (Z)-oct-4-ene 

Relevant articles and documents

Regioselective carbon-carbon bond formation in titanium mediated reaction of ethylmagnesium bromide with allylic alcohols and allylic ethers

In the presence of Ti(Oi-Pr)4 reaction of EtMgBr with allylic alcohols and allylic ethers affords the products of formal SN2′ substitution of hydroxy or alkoxy groups with ethyl groups in moderate to good yields and excellent regiose

OLEFIN METATHESIS CATALYSTS

This invention relates generally to metathesis catalysts and the use of such catalysts in the metathesis of olefins and olefin compounds, more particularly, in the use of such catalysts in Z and E selective olefin metathesis reactions. The invention has utility in the fields of organometallics and organic synthesis.

High Trans Kinetic Selectivity in Ruthenium-Based Olefin Cross-Metathesis through Stereoretention

The first kinetically controlled, highly trans-selective (>98%) olefin cross-metathesis reaction is demonstrated using Ru-based catalysts. Reactions with either trans or cis olefins afford products with highly trans or cis stereochemistry, respectively. This E-selective olefin cross-metathesis is shown to occur between two trans olefins and between a trans olefin and a terminal olefin. Additionally, new stereoretentive catalysts have been synthesized for improved reactivity. (Chemical Equation Presented).