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Neohexene

Index Neohexene

Neohexene is the organic compound with the formula (CH3)3CCH. [1]

10 relations: Carbon–hydrogen bond activation, Ethenolysis, Hexene, Journal of the American Chemical Society, Olefin metathesis, Organic compound, P-Cymene, Synthetic musk, Terbinafine, Wiley-VCH.

Carbon–hydrogen bond activation

Carbon–hydrogen bond functionalization (C–H functionalization) is a type of reaction in which a carbon–hydrogen bond is cleaved and replaced with a carbon-X bond (where X is usually carbon, oxygen, or nitrogen).

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Ethenolysis

Ethenolysis is a chemical process in which internal olefins are degraded using ethylene as the reagent.

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Hexene

Hexene is an alkene with a molecular formula C6H12.

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Journal of the American Chemical Society

The Journal of the American Chemical Society (also known as JACS) is a weekly peer-reviewed scientific journal that was established in 1879 by the American Chemical Society.

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Olefin metathesis

Olefin metathesis is an organic reaction that entails the redistribution of fragments of alkenes (olefins) by the scission and regeneration of carbon-carbon double bonds.

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Organic compound

In chemistry, an organic compound is generally any chemical compound that contains carbon.

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P-Cymene

p-Cymene is a naturally occurring aromatic organic compound.

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Synthetic musk

Synthetic musks, known as white musks in the perfume industry, are a class of synthetic aroma compounds to emulate the scent of deer musk and other animal musks (ambergris, castoreum and civet).

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Terbinafine

Terbinafine, sold under the brand name Lamisil among others, is an antifungal medication used to treat ringworm, pityriasis versicolor, and fungal nail infections.

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Wiley-VCH

Wiley-VCH is a German publisher owned by John Wiley & Sons.

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Redirects here:

2,2-Dimethylbutene, 3.3-Dimethylbutene, T-butylethylene, Tert-butylethylene.

References

[1] https://en.wikipedia.org/wiki/Neohexene

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