20063-92-7

Basic information

• Product Name: TRANS-3-NONENE
• Synonyms: 3-NONENE;TRANS-3-NONENE;(E)-3-C9H18;(E)-3-Nonene;trans-non-3-ene;(E)-non-3-ene;3-Nonene, (E)-;Nsc97534
• CAS NO: 20063-92-7
• Molecular Formula: C₉H₁₈
• Molecular Weight: 126.24
• EINECS: 243-495-0
• Mol File: 20063-92-7.mol
• Article Data: 16

Chemical Properties

• Melting Point: -89.14°C (estimate)
• Boiling Point: 147.55°C
• Flash Point: 90 °F
• Appearance: /
• Density: 0.734 g/mL at 25 °C(lit.)
• Vapor Pressure: 6.06mmHg at 25°C
• Refractive Index: n20/D 1.419(lit.)
• CAS DataBase Reference: TRANS-3-NONENE(CAS DataBase Reference)
• NIST Chemistry Reference: TRANS-3-NONENE(20063-92-7)
• EPA Substance Registry System: TRANS-3-NONENE(20063-92-7)

Safety Data

• Statements: 10
• Safety Statements: 16-29-33
• RIDADR: UN 3295 3/PG 3
• WGK Germany: 3
• HazardClass: 3.2
• PackingGroup: III
• Hazardous Substances Data: 20063-92-7(Hazardous Substances Data)

Usage

General Description

TRANS-3-NONENE is a colorless liquid hydrocarbon with a chemical formula of C9H18. It is an unsaturated hydrocarbon with a trans configuration at the third carbon-carbon double bond. TRANS-3-NONENE is primarily used as a flavoring agent in the food industry, providing a fruity and green aroma often used in beverages and fragrances. It is also used as a synthetic intermediate in the production of other chemicals and as a solvent in various industrial processes. Due to its low toxicity and pleasant odor, TRANS-3-NONENE is considered relatively safe for use in consumer products when properly handled and manufactured.

InChI:InChI=1/C9H18/c1-3-5-7-9-8-6-4-2/h5,7H,3-4,6,8-9H2,1-2H3/b7-5-

Upstream product

• 693-03-8 n-butyl magnesium bromide 
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• 66-25-1 hexanal 
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• 35349-80-5 (E)-1-bromo-2-heptene 
• 925-90-6 ethylmagnesium bromide 
• 185019-15-2 nonan-3-ol 

Downstream Products

• 37596-38-6 2-ethyl-octanal 
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Relevant articles and documents

SELECTIVITY IN ALLYLIC SUBSTITUTIONS WITH ORGANOMETALLICS THROUGH NEIGHBOURING COORDINATION. SYNTHESIS AND REACTIONS OF COPPER(I) ?-COMPLEXES WITH 2-ALLYLLOXYBENZOTHIAZOLES

2-Allylloxybenzothiazoles react with CuBr to give stable CuI ?-complexes.These complexes undergo nucleophilic attack by organomagnesium compounds to give olefins with very high regio- and stereo-specificity.

Highly enantioselective Cu-catalysed allylic substitutions with Grignard reagents

A catalyst system able to perform highly enantioselective Cu-catalysed allylic alkylations with Grignard reagents is described. The Royal Society of Chemistry 2006.

Zirconium porphyrins as novel active catalysts for highly regio- And stereoselective ethylalumination of alkynes

Zirconium(IV) complexes of 5, 10, 15, 20-tetraphenylporphyrin ((TPP)ZrX2) catalyze highly regioand stereo-selective ethylalumination of terminal alkynes with satisfactorily high turnover numbers.