Fenpentadiol

Application Refer to the product&#8242s Certificate of Analysis for more information on a suitable instrument technique. Contact Technical Service for further support.

(+)-Fenchone

(-)-Fenchone

Application Starting material for asymmetric epoxidation. Substrate employed in a synthesis of amino-substituted dienes via a bismuth-catalyzed S N i displacement of alcohols by sulfonamide nucleophiles.

Application Starting material for asymmetric epoxidation. Substrate employed in a synthesis of amino-substituted dienes via a bismuth-catalyzed S N i displacement of alcohols by sulfonamide nucleophiles.

15-Hydroxypentadecanoic acid is an &#969-hydroxy acid. One of the method reported for its synthesis is from 1,12-dodecanolide.

3,4-Pentadien-1-ol

Application Refer to the product&#8242s Certificate of Analysis for more information on a suitable instrument technique. Contact Technical Service for further support.

This certified reference material (CRM) is produced and certified in accordance with ISO/IEC 17025 and ISO 17034 . The CRM is traceable to primary material from an NMI, e.

Trans-1,3-Pentadiene spectra is recorded in the 5000-17500 cm(-1) region with conventional and intracavity laser photoacoustic spectroscopy . It can be determined by the spectrophotometric method based on the Diels-Alder reaction.

Trans-1,3-Pentadiene spectra is recorded in the 5000-17500 cm(-1) region with conventional and intracavity laser photoacoustic spectroscopy . It can be determined by the spectrophotometric method based on the Diels-Alder reaction.