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(S)-(+)-4-Penten-2-ol, 97%, Thermo Scientific Chemicals
Catalog number: B25728.03
1 g, Each
Thermo Scientific Chemicals
(S)-(+)-4-Penten-2-ol, 97%, Thermo Scientific Chemicals
Catalog number: B25728.03
1 g, Each
Quantity
Catalog number: B25728.03
also known as B25728-03
Price (USD)
Price: 169.00
Online price: 145.65
Your price:
Quantity
-
Chemical Identifiers
CAS
55563-79-6
IUPAC Name
pent-4-en-2-ol
Molecular Formula
C5H10O
InChI Key
ZHZCYWWNFQUZOR-UHFFFAOYNA-N
SMILES
CC(O)CC=C
Specifications
Specification SheetAppearance (Color)
Clear colorless
Assay (GC)
≥96.0%
Refractive Index
1.4215-1.4265 @ 20?C
Form
Liquid
Optical Rotation
5.1 ± 0.2? ( C = 1 in chloroform )
Description
(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 originally part of the Alfa Aesar product portfolio. Some documentation and label information may refer to the legacy brand. The original Alfa Aesar product / item code or SKU reference has not changed as a part of the brand transition to Thermo Scientific Chemicals.
Applications
(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.
Notes
Incompatible with strong oxidizing agents.
(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.
Notes
Incompatible with strong oxidizing agents.
RUO – Research Use Only
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