5394-77-4

Upstream product

• 50423-29-5 O-dimethyl-4-pentadecylcatechol 
• 116082-33-8 5-pentadecyl-benzo[1,3]dioxole 
• 112-71-0 1-Bromotetradecane 
• 5447-02-9 3,4-dibenzyloxybenzaldehyde 
• 120-14-9 3,4-dimethoxy-benzaldehyde 
• 100486-23-5 1-(3,4-dimethoxyphenyl)pentadecan-1-ol 
• 52122-74-4 3-pentadecylphenyl acetate 
• 15071-57-5 Methyl 3-n-pentadecylphenyl ether 
• 501-24-6 3-n-Pentadecylphenol 
• 7647-01-0 hydrogenchloride 
• 10035-10-6 hydrogen bromide 
• 265310-64-3 4-n-pentadecyl-1,2-benzoquinone 
• 133950-57-9 1-(3,4-Bis-benzyloxy-phenyl)-pentadecan-1-ol 

Downstream Products

• 57-10-3 1-hexadecylcarboxylic acid 

Relevant academic research and scientific papers

A new and efficient synthesis of ortho- and para-benzoquinones of cardanol derivatives by the catalytic system MeReO3-H2O2

A novel and efficient synthesis of ortho- and para-benzoquinones of cardanol derivatives was carried using catalytic system MeReO3-H2O2. The effect of the presence of bromine atoms on the selectivity of the oxidation was also studied. It was observed that the regio-selectivity of the reaction depends on the nature and on the substitution pattern of the substituents.

Analogues of Poison Ivy Urushiol. Synthesis and Biological Activity of Disubstituted n-Alkylbenzenes

The total synthesis of different isomers and analogues of poison ivy urushiol is described.These include the positional isomers 1-5 and the nitrogen-containing analogues 6 and 8 and their mesylamino derivatives 7 and 9. 3,4-Dimethoxybenzaldehyde, m-dimeth