172294-15-4

Upstream product

• 139258-85-8 9-(tert-butyldiphenylsilyloxy)-nonan-1-ol 
• 3937-56-2 1,9-Nonanediol 
• 58479-61-1 tert-butylchlorodiphenylsilane 
• 55362-80-6 9-bromononan-1-ol 

Downstream Products

• 1391985-67-3 tert-butyl(9-iodononyloxy)diphenylsilane 
• 1391985-73-1 11-(tert-butyldiphenylsilyloxy)-N-methoxy-N-methyl-2-(prop-1-en-2-yl)undecanamide 
• 55362-80-6 9-bromononan-1-ol 

Relevant academic research and scientific papers

Synthesis of the esterified cerebroside in the epidermis of guinea pigs.

(2S,3R,4E,23'Z)-1-O-(beta-D-Glucopyranosyl)-N-(32'-linoleoyloxy -23'-dotriacontenoyl)-4-sphingenine (1), a component of the esterified cerebrosides in the epidermis of guinea pigs, was synthesized by selective N-acylation of (2S,3R,4E)-1-O-(beta-D-glucopy

Efficient macrocyclization by a novel oxy-oxonia-cope reaction: Synthesis and olfactory properties of new macrocyclic musks

Musk made to odor: A new oxy-oxonia-Cope macrocyclization to (3Z)-configured cycloalk-3-en-1-yl formates is reported, which is useful in the synthesis of unsaturated and saturated macrocyclic ketones (see scheme). The synthesized structures provide new insight into the structure-odor correlation of musks, making it likely for macrocyclic and linear alicyclic musks to address the same olfactory receptors.