3 Hexyne
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3 hexyne is the organic compound with the formula c 2 h 5 ccc 2 h 5.
3 hexyne. Structure of the coordination complex nbcl 3 dimethoxyethane 3 hexyne. This reaction will need catelyst rh 2 oac 4 and the menstruum ch 2 cl 2. Use of the information documents and data from the echa website is subject to the terms and conditions of this legal notice and subject to other binding limitations provided for under applicable law the information documents and data made available on the echa website may be reproduced distributed and or used totally or in part for non commercial purposes provided that echa is. It is a reagent in organometallic chemistry.
Packaging 5 25 g in glass bottle. C 2 h 5 c cc 2 h 5. It can react with diazoacetic acid ethyl ester to produce 1 2 diaethyl 3 aethoxycarbonyl cycloprop 1 en. 3 hexyne was used in the synthesis of fused hetero hydropyridyl ligands bonded to the ru p cymene organometallic moiety by reacting with ruthenacycles.
Validated by experts validated by users non validated removed by users. A chemical structure of a molecule includes the arrangement of atoms and the chemical bonds that hold the atoms together. 3 hexyne forms with 5 decyne 4 octyne and 2 butyne a series of symmetric alkynes. It was also used in the preparation of 4 2 cycloaddition product by reacting with borole.
Concentration information is not available for this spectrum and therefore molar absorptivity values cannot be derived. Images of the chemical structure of 3 hexyne are given below. 3 hexyne french acd index name acd iupac name 928 49 4 rn diethylacetylene. You should be cautious while dealing with this chemical.
3 hexyne 2 5 dimethyl c8h14 cid 136716 structure chemical names physical and chemical properties classification patents literature biological activities. Mfcd00009381 mdl number 1 2 diethylacetylene. The reaction time is 3 hours and the yield is about 68. This colorless liquid is one of three isomeric hexynes.
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