CAS 50639-00-4
:2-Ethyl-2-hexen-1-ol
Description:
2-Ethyl-2-hexen-1-ol, with the CAS number 50639-00-4, is an organic compound classified as an alcohol due to the presence of a hydroxyl (-OH) functional group. It features a branched carbon chain, specifically a hexene structure with an ethyl group at the second carbon position, contributing to its unique properties. This compound is typically a colorless liquid at room temperature and possesses a characteristic odor. It is soluble in organic solvents and exhibits limited solubility in water, which is common for larger alcohols. 2-Ethyl-2-hexen-1-ol can participate in various chemical reactions, including dehydration and oxidation, making it useful in organic synthesis and as a potential intermediate in the production of other chemicals. Its applications may extend to the fragrance and flavor industry, as well as in the formulation of certain polymers. Safety data should be consulted for handling and exposure guidelines, as with any chemical substance.
Formula:C8H16O
InChI:InChI=1S/C8H16O/c1-3-5-6-8(4-2)7-9/h6,9H,3-5,7H2,1-2H3
InChI key:InChIKey=JSRFYJBJQPGAAA-UHFFFAOYSA-N
SMILES:C(=CCCC)(CC)CO
Synonyms:- (2E)-2-ethylhex-2-en-1-ol
- 2-Ethyl-2-hexen-1-ol
- 2-Ethyl-2-hexenol
- 2-Ethylhex-2-En-1-Ol
- 2-Hexen-1-ol, 2-ethyl-
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Found 4 products.
2-Ethyl-2-hexenol (~85%)
CAS:Controlled Product<p>Applications 2-Ethyl-2-hexenol is an intermediate in the synthesis of 2-(Chloromethyl)-1-butene (C368570). 2-(Chloromethyl)-1-butene is a useful reagent for palladium(II)-catalyzed intramolecular tandem aminoalkylation. It can also be used to prepare (±)-Stemonamine and (±)-Cephalotaxine.<br>References Du, W., etal.: J. Am. Chem. Soc. 137, 1130 (2015); Zhao, Y., et al.: J. Org. Chem 74, 3211 (2009)<br></p>Formula:C8H16OPurity:>85%Color and Shape:NeatMolecular weight:128.21
