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3-Octene, 2-methyl-, (Z)-, also known as (Z)-2-Methyl-3-octene, is an organic compound with the molecular formula C9H18. It is a colorless liquid with a strong, pungent odor. This unsaturated hydrocarbon belongs to the class of alkenes, characterized by the presence of a carbon-carbon double bond. The double bond in 3-Octene, 2-methyl-, (Z)- is located between the third and fourth carbon atoms, and the molecule has a Z (cis) configuration, indicating that the two highest priority groups are on the same side of the double bond. 3-Octene, 2-methyl-, (Z)- is used as a fragrance ingredient and a chemical intermediate in the synthesis of various organic compounds. It is also found in trace amounts in some natural products, such as essential oils.

62862-21-9

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62862-21-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 62862-21-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,2,8,6 and 2 respectively; the second part has 2 digits, 2 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 62862-21:
(7*6)+(6*2)+(5*8)+(4*6)+(3*2)+(2*2)+(1*1)=129
129 % 10 = 9
So 62862-21-9 is a valid CAS Registry Number.

62862-21-9Downstream Products

62862-21-9Relevant academic research and scientific papers

Unique variations of the distribution coefficients of homologues in the perfluorodecalin-acetonitrile heterophase system

Zenkevich,Kushakova

experimental part, p. 337 - 344 (2011/06/27)

The properties of the heterophase system perfluorodecalin-acetonitrile differ significantly from those of other combinations of the organic solvents limitedly soluble in each other. While for the most of such combinations the distribution coefficients (K d) of homologues increase in going from the simplest to next members of the series, in the case of perfluorodecalin- acetonitrile they remain almost constant. This provides a possibility to use the values of K d directly for the group identification of analytes, and first of all allows distinguishing isomeric alkenes and cycloalkanes, as well as the isomers of the hydrocarbons with greater formal unsaturation.

Reactions of α-epoxysilanes with organocopper reagents. A stereoselective route to alkenes

Chauret, Denise C.,Chong, J. Michael

, p. 3695 - 3698 (2007/10/02)

Reactions of α-epoxysilanes with cuprate reagents can be controlled to give β-silyl alcohols as major products. An oxidation, Grignard addition, and elimination sequence then provides alkenes with up to 98% de.

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