72587-79-2

Upstream product

• 65492-28-6 o-benzoquinone bis(dimethyl acetal) 
• 82895-26-9 C₁₇H₃₅Li 
• 54636-77-0 2,3-dimethoxybenzyl bromide 
• 5653-67-8 2,3-dimethoxybenzyl alcohol 
• 872-26-4 hexadecylmagnesium bromide 
• 859977-30-3 1-(2,3-dimethoxy-phenyl)-heptadecan-1-ol 

Downstream Products

• 75776-33-9 3-heptadecylbenzoquinone 
• 75776-35-1 3-heptadecyl-5-(pentylamino)-1,2-benzoquinone 
• 75776-36-2 3-Heptadecyl-5-pentylamino-benzene-1,2-diol 
• 75785-50-1 N-acetyl-S-(2,3-dihydroxy-4-heptadecylphenyl)cysteine 
• 75776-37-3 Acetic acid 2-acetoxy-5-(acetyl-pentyl-amino)-3-heptadecyl-phenyl ester 
• 87328-79-8 (S)-2-tert-Butoxycarbonylamino-propionic acid 2-((S)-2-tert-butoxycarbonylamino-propionyloxy)-6-heptadecyl-phenyl ester 
• 76619-72-2 diacetyl-3-n-heptadecylcatechol 
• 5862-27-1 3-heptadecylbenzene-1,2-diol (hydrolaccol) 

Relevant academic research and scientific papers

Compositions for prevention/prophylactic treatment of poison ivy dermatitis

The present invention, in one or more embodiments, comprises water-soluble derivatives of 3-n-pentadecylcatechol (poison ivy urushiol saturated congener) and/or 3-n-heptadecylcatechol (poison oak urushiol saturated congener) as compositions for the prevention and/or prophylactic treatment of contact dermatitis caused by poison ivy and poison oak. The present invention is also directed towards processes for making such compounds. Disclosed are compounds which are effective for tolerizing and desensitizing a subject against allergens contained in plants of the Anacardiaceae and Ginkgoaceae families comprising water soluble urushiol esters of general formula (I) tolerizing and desensitizing mammals, including humans, to allergens contained in plants of the Anacardiaceae and Ginkgoaceae families is attained by administering a composition containing at least one water soluble urushiol ester compound.

Synthesis and antiallergenic properties of 3-n-pentadecyl- and 3-n-heptadecylcatechol esters

A synthetic procedure is described for the preparation of 3-n-pentadecyl- and 3-n-heptadecylcatechols and their acetate and alaninate esters. The Wittig reagent prepared from 2,3-dimethoxybenzyltriphenylphosphonium bromide (III) was coupled with 1-tetrade

REACTION OF o-BENZOQUINONE BISACETALS WITH ORGANOLITHIUMS. A NOVEL ROUTE TO SUBSTITUTED VERATROLES

Substituted veratroles were easily obtained by the reaction of o-benzquinone bisacetals with organolithiums.