92829-72-6

Usage

Uses

Used in Perfumery Industry:
Magnaldehyde B is used as a fragrance ingredient for its sweet, floral, and slightly balsamic odor, contributing to the overall scent profile of perfumes and colognes.
Used in Cosmetic Products:
Magnaldehyde B is used as a scent enhancer in cosmetic products to provide a pleasant and long-lasting aroma, improving the sensory experience for users.
Used in Fragrance Creation:
Magnaldehyde B is used as a valuable component in the creation of perfumes and colognes, enhancing the longevity and scent profile of these fragrances.

Upstream product

• 2973-78-6 3-bromo-4-hydroxybenzylaldehyde 
• 123-08-0 4-hydroxy-benzaldehyde 
• 112996-33-5 4-allyloxy-2'-benzyloxy-5'-(E)-(2-formylethenyl)biphenyl 
• 4572-26-3 1-oxaspiro[4,5]deca-6,9-dien-2,8-dione 
• 113016-76-5 4-allyloxy-2'-benzyloxy-5'-(2-methoxycarbonylethyl)biphenyl 
• 112996-32-4 4-allyloxy-2'-benzyloxy-5'-(E)-(2-methoxycarbonylethyl)biphenyl 
• 112639-29-9 4-allyloxy-2'-hydroxy-5'-(2-methoxycarbonylethyl)biphenyl 

Relevant academic research and scientific papers

Synthesis of magnaldehydes B and e and dictyobiphenyl B by microwave-promoted cross-coupling of boronophenols

Magnaldehydes B and E along with their 4′-methylated derivatives are naturally occurring 2,4′-biphenols that have been isolated from the Magnoliaceae. Herein, these natural products have been synthesized from a common intermediate, which was obtained by a microwave-promoted, heterogeneously catalyzed, and protecting-group-free Suzuki-Miyaura coupling reaction in an aqueous medium. These reaction conditions were also successfully applied to a one-step synthesis of the slime mold metabolite dictyobiphenyl B. A protecting-group-free Suzuki-Miyaura cross-coupling reaction of halophenols and boronophenols by using Pd/C as the catalyst and water as the solvent under microwave irradiation has been used for the synthesis of five biphenol-type natural products.

An Approach for General Synthesis of Biphenyl Neolignans by the Reaction of 1-Oxaspirodeca-6,9-diene-2,8-dione with the Grignard Reagent and Synthesis of Magnaldehyde B

An approach for general synthesis of biphenyl neolignans by the reactionof 1-oxaspiro-deca -6,9-diene-2,8-dione (3) (quinol-lactone) with the Grignard reagent 4 was explored.Among the biphenyl derivatives 6,8 and 9 thus obtained, 6 was transformed to magnaldehyde B (2b) in three steps.Keywords---biphenyl neolignan; synthesis; magnaldehyde B; quinol-lactone; Grignard reagent