CAS 55563-79-6
:(S)-2-Hydroxypent-4-ene
Description:
(S)-2-Hydroxypent-4-ene is an organic compound characterized by its hydroxyl (-OH) group and a double bond within its carbon chain. As a chiral molecule, it exists in two enantiomeric forms, with the (S) configuration indicating the specific spatial arrangement of its atoms. This compound features a five-carbon backbone with a double bond located between the fourth and fifth carbons, contributing to its unsaturation. The presence of the hydroxyl group makes it an alcohol, which can participate in various chemical reactions, including dehydration and oxidation. Its structure allows for potential applications in organic synthesis and as an intermediate in the production of more complex molecules. The compound's physical properties, such as boiling point and solubility, are influenced by the functional groups present and the overall molecular structure. Additionally, (S)-2-Hydroxypent-4-ene may exhibit specific biological activities, making it of interest in pharmaceutical and biochemical research.
Formula:C5H10O
InChI:InChI=1/C5H10O/c1-3-4-5(2)6/h3,5-6H,1,4H2,2H3/t5-/m0/s1
SMILES:C=CC[C@H](C)O
Synonyms:- (2S)-pent-4-en-2-ol
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Found 4 products.
Ref: IN-DA003CHF
1g182.00€5g566.00€10gTo inquire50gTo inquire100gTo inquire250gTo inquire100mg73.00€250mg114.00€(S)-(+)-2-Hydroxypent-4-ene
CAS:(S)-(+)-2-Hydroxypent-4-enePurity:98%Color and Shape:Colourless LiquidMolecular weight:86.13g/mol(S)-(+)-4-Penten-2-ol, 97%
CAS:(S)-(+)-4-Penten-2-ol is involved in the synthesis of goniothalamin, hexadecanolide, massoia lactone, and parasorbic acid through sequential allylboration-esterification ring-closing metathesis reactions. It is also used to prepare 2-pentanone. This Thermo Scientific Chemicals brand product was orig
Formula:C5H10OPurity:97%Color and Shape:Clear colorless, LiquidMolecular weight:86.13
