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(3E)-hex-3-ene-1,5-diyne is an organic compound with the molecular formula C8H8. It is a conjugated diene-yne, characterized by the presence of two triple bonds (one in the 1-position and the other in the 5-position) and a double bond in the 3-position. This molecule is known for its unique electronic structure and reactivity, which can participate in various chemical reactions such as Diels-Alder reactions and other cycloadditions. The (3E)-configuration indicates that the double bond has a trans (E) geometry, which can influence the molecule's physical properties and reactivity. (3E)-hex-3-ene-1,5-diyne is a versatile building block in organic synthesis and is used in the preparation of various complex organic molecules.

6929-94-8

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6929-94-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 6929-94-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,9,2 and 9 respectively; the second part has 2 digits, 9 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 6929-94:
(6*6)+(5*9)+(4*2)+(3*9)+(2*9)+(1*4)=138
138 % 10 = 8
So 6929-94-8 is a valid CAS Registry Number.

6929-94-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name hex-3-ene-1,5-diyne

1.2 Other means of identification

Product number -
Other names 3-Hexen-1,5-diin

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:6929-94-8 SDS

6929-94-8Downstream Products

6929-94-8Relevant academic research and scientific papers

UV laser photodeposition of nanomagnetic soot from gaseous benzene and acetonitrile-benzene mixture

Pola, Josef,Ouchi, Akihiko,Mary?ko,Vorlí?ek,?ubrt, Jan,Bakardjieva,Bastl, Zdeněk

experimental part, p. 188 - 194 (2012/02/02)

Megawatt KrF laser gas-phase photolysis of benzene and acetonitrile-benzene mixture was studied by using mass spectroscopy-gas-chromatography and Fourier transform infrared spectroscopy for analyses of volatile products, and by Fourier transform infrared, Raman and X-ray photoelectron spectroscopy, electron microscopy and magnetization measurements for analyses of solid products deposited from the gas-phase. The results are consistent with carbonization of benzene and decomposition of non-absorbing acetonitrile in carbonizing benzene through collisions with excited benzene and/or its fragments. The solid products from benzene and acetonitrile-benzene mixture have large surface area and are characterized as nanomagnetic amorphous carbonaceous soot containing unsaturated C centers prone to oxidation. The nanosoot from acetonitrile-benzene mixture incorporates CN groups, confirms reactions of benzene fragments with CN radical and has a potential for modification by reactions at the CN bonds.

Highly Efficient Photochemical Synthesis of the Enediyne Functionality via a Norrish Type II Reaction

Nuss, John M.,Murphy, Martin M.

, p. 37 - 40 (2007/10/02)

A photochemical synthesis of enediynes utilizing the Norrish Type II reaction is described.The application of this strategy to the synthesis of cyclic and acyclic enediynes from readily available precursors is discussed.

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