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(E)-2-Hexen-4-yne is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

33625-96-6

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33625-96-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 33625-96-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,3,6,2 and 5 respectively; the second part has 2 digits, 9 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 33625-96:
(7*3)+(6*3)+(5*6)+(4*2)+(3*5)+(2*9)+(1*6)=116
116 % 10 = 6
So 33625-96-6 is a valid CAS Registry Number.

33625-96-6SDS

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 hexa-4-en-2-yne

1.2 Other means of identification

Product number -
Other names hex-2t-en-4-yne

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:33625-96-6 SDS

33625-96-6Downstream Products

33625-96-6Relevant academic research and scientific papers

Study of Methylidyne Radical (CH and CD) Reaction with 2,5-Dimethylfuran Using Multiplexed Synchrotron Photoionization Mass Spectrometry

Carrasco, Erica,Meloni, Giovanni

, p. 6118 - 6133 (2018/07/09)

At 298 K the reactions of 2,5-dimethlyfuran + CH(X2Θ) and + CD radicals were investigated using synchrotron radiation coupled with multiplexed photoionization mass spectrometry at the Lawrence Berkeley National Laboratory. Reaction products wer

METAL COMPLEXES WITH ALLYLANILINES. IV. SYNTHESIS AND REACTIVITY OF RHODIUM(I) COMPLEXES WITH 2-ALLYLANILINE AND N-ALLYLANILINE

Aresta, M.,Fazio, M. De

, p. 109 - 120 (2007/10/02)

The reaction of 2-allylaniline (2aa) with 2 (I) in toluene or benzene at room temperature affords the dimer 2 (II) in which the ligand acts as bidentate, being coordinated to the metal through the N atom and the olefinic group.II in CH2Cl2, isomerizes 2aa to trans-2-propenylaniline.This reaction goes also catalytically.Heating of II in benzene affords 2-methyl-indoline.N-Allylaniline (naa) reacts with I to give the deep violet diamagnetic complex Rh2Cl2(naa)3 (III), which is converted slowly into 2.When III is heated with an excess of naa, the ligand is catalytically transformed into propene, azobenzene, N-n-propylaniline, N-i-propylaniline, N-allylideneaniline and aniline, as the more abundant products.Moreover, III reacts with diphenylacetylene to afford 2,5-dihydro-1,2,3-triphenyl-4-methyl-pyrrole.The reaction of III with methylacetylene follows a more complex path, and products of dimerization and trimerization of the alkyne have been isolated.Carbon dioxide influences the oligomerization reaction.

SOME CATALYTIC PROPERTIES OF Rh(diphos)(η-BPh4)

Albano, P.,Aresta, M.

, p. 243 - 246 (2007/10/02)

The covalent complex Rh(diphos)(η-BPh4) (I) reacts with CO in polar solvents to afford the cationic dicarbonyl cis-(BPh4).I is an effective catalyst for methylacetylene oligomerization and allene polymerization.In the presence of CO2 and methylacetylene, I affords 4,6-dimethyl-2-pyrone.

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