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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. Due to its low toxicity and pleasant odor, it is considered relatively safe for use in consumer products when properly handled and manufactured.
Used in Food Industry:
TRANS-3-NONENE is used as a flavoring agent for providing a fruity and green aroma in beverages and fragrances.
Used in Chemical Production:
TRANS-3-NONENE is used as a synthetic intermediate in the production of other chemicals.
Used in Industrial Processes:
TRANS-3-NONENE is used as a solvent in various industrial processes.

20063-92-7

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20063-92-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 20063-92-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,0,0,6 and 3 respectively; the second part has 2 digits, 9 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 20063-92:
(7*2)+(6*0)+(5*0)+(4*6)+(3*3)+(2*9)+(1*2)=67
67 % 10 = 7
So 20063-92-7 is a valid CAS Registry Number.
InChI:InChI=1/C9H18/c1-3-5-7-9-8-6-4-2/h5,7H,3-4,6,8-9H2,1-2H3/b7-5-

20063-92-7SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name (E)-non-3-ene

1.2 Other means of identification

Product number -
Other names EINECS 243-495-0

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:20063-92-7 SDS

20063-92-7Relevant academic research and scientific papers

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

Calo, Vincenzo,Lopez, Luigi,Pesce, Giannangelo

, p. 179 - 184 (1982)

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.

A General Approach to Intermolecular Olefin Hydroacylation through Light-Induced HAT Initiation: An Efficient Synthesis of Long-Chain Aliphatic Ketones and Functionalized Fatty Acids

Guin, Joyram,Paul, Subhasis

supporting information, p. 4412 - 4419 (2021/02/05)

Herein, an operationally simple, environmentally benign and effective method for intermolecular radical hydroacylation of unactivated substrates by employing photo-induced hydrogen atom transfer (HAT) initiation is described. The use of commercially available and inexpensive photoinitiators (Ph2CO and NHPI) makes the process attractive. The olefin hydroacylation protocol applies to a wide array of substrates bearing numerous functional groups and many complex structural units. The reaction proves to be scalable (up to 5 g). Different functionalized fatty acids, petrochemicals and naturally occurring alkanes can be synthesized with this protocol. A radical chain mechanism is implicated in the process.

Highly enantioselective Cu-catalysed allylic substitutions with Grignard reagents

Lopez, Fernando,Van Zijl, Anthoni W.,Minnaard, Adriaan J.,Feringa, Ben L.

, p. 409 - 411 (2008/02/05)

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

Shibata, Kenji,Aida, Takuzo,Inoue, Shohei

, p. 1077 - 1080 (2007/10/02)

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.

THE HYDRIDOPENTACYANOCOBALTATE ANION INDUCED DEOXYGENATION OF ALLYLIC ALCOHOLS USING β-CYCLODEXTRIN AS A PHASE TRANSFER AGENT

Lee, Jong-Tae,Alper, Howard

, p. 4101 - 4104 (2007/10/02)

β-Cyclodextrin promotes the deoxygenation of allylic alcohols to olefins using hydrogen and the in situ generated hydridopentacyanocobaltate anion.Internal olefins, of trans-stereochemistry, are the principal reaction products (i. e., no cis-products are formed).

CROSS-COUPLIN REACTIONS BETWEEN SOME ALLYL, HOMOALLYL, AND HOMOPROPARGYL SUBSTRATES AND TRIALKYLALANES OR DIALKYL- AND DIARYL-MAGNESIUM DERIVATIVES

Tolstikov, G. A.,Dzhemilev, U. M.

, p. 133 - 144 (2007/10/02)

Trialkylalanes and dilkyl- and diaryl-magnesium derivatives can be cross-coupled with allyl ethers and esters, sulphides, and quaternized allylamines.The reactions proceed uncatalyzed either with mild conditions or in the presence of copper complex catalysts to result in high yields of mono- and di-olefins of various structures.The alkylation of homoallyl or homopropargyl tosylates by trialkylalanes is accompanied by cyclization, which leads to alkyl-substituted cyclopropanes. i.e. cyclobutanes and cyclopropylidenes.

Selectivity in the Allylic Substitutions with Organometallics through Neighboring Coordination. 2-(Allyloxy)benzothiazoles as SN2' Electrophiles for Regio- and Stereoselective Olefin Syntheses

Calo, Vincenzo,Lopez, Luigi,Pesce, Giannangelo,Calianno, Antonia

, p. 4482 - 4485 (2007/10/02)

An efficient control of the regio- and stereochemistry in the allylic substitutions with organomagnesium compounds has been achieved by using 2-(allyloxy)benzothiazoles as substrates in the presence of copper bromide.The selectivity is due to the coordinative effects of the substrates toward the organometallic species.

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