28941-56-2

Upstream product

• 67-56-1 methanol 
• 96258-02-5 (7R,9Z)-octadec-9-en-7-ol 
• 101-34-8 castor oil acetate 

Downstream Products

• 76904-91-1 (R)-3-((R)-3,3,3-Trifluoro-2-methoxy-2-phenyl-propionyloxy)-nonanoic acid methyl ester 
• 694528-02-4 N-((3R)-3-[Boc-L-allo-Thr(TBS)-GlyO]-nonanoyl)-N-Me-L-Leu-L-allo-Ile-L-Ser(Bn)-OAllyl 
• 694528-16-0 3-demethyl-24-O-benzyl-globomycin 
• 694527-88-3 N-((3R)-3-hydroxynonanoyl)-N-Me-L-Leu-L-allo-Ile-L-Ser(Bn)-OAllyl 
• 121541-65-9 (R)-(-)-1,3-nonandiol 1 

Relevant academic research and scientific papers

Ozonolysis of alkenes and study of reactions of polyfunctional compounds: LXVIII. Investigation of transformations of peroxide products of olefins ozonolysis treated with hydroxylamine hydrochloride

Hydroxylamine hydrochloride efficiently reduces peroxide products of olefins ozonolysis into carbonyl compounds. Depending on the substrate character, solvent, and the treatment conditions the arising aldehydes transformed along the route aldehyde→aldoxime→nitrile→ester into individual compounds or their mixtures, or give the corresponding acetals.

Ozonolytic transformations of olefinic derivatives of L-menthol and ricinolic acid

Ozonolysis and reduction of olefinic derivatives of ricinolic acid and L-menthol were studied using hydroxylamine hydrochloride and sodium trisacetoxyborohydride to reduce the peroxide products.