116754-72-4

Upstream product

• 536-74-3 phenylacetylene 
• 85070-62-8 12-bromo-1-phenyl-dodec-1-yne 
• 4101-68-2 1,10-dibromodecane 
• 85070-63-9 1-bromo-12-phenyl-dodecane 
• 116754-69-9 14-phenyl-2(RS)-methyltetradecan-1-ol 
• 98-59-9 p-toluenesulfonyl chloride 
• 116754-65-5 2-Methyl-14-phenyl-tetradecanoic acid methyl ester 
• 116754-61-1 2-Methyl-14-phenyl-tetradecanoic acid 

Downstream Products

• 88336-88-3 Methyl 15-Phenyl-3(R,S)-methylpentadecanoate 
• 116754-80-4 15-Phenyl-3(R,S)-methylpentadecanoic Acid 
• 116754-75-7 14-phenyl-2(RS)-methyltetradecanenitrile 

Relevant academic research and scientific papers

Methode de synthese d'acides gras marques substitues ou non en α et en β

2-Propyn-1-ol and the dibromides Br(CH2)nBr (n = 10-12) have been used as starting materials for the synthesis of α- and β-methyl-branched fatty acids (C16) labeled with 123I at the ω-position.The methyl groups are introduced through the use of the lithium salt of either propanoic or isobutyric acid.The synthesis of *IC6H5(CH2)14COOH and *IC6H5(CH2)12CH(CH3)CH2COOH have been achieved in the same way starting from phenylacetylene.In each case, the radioactive iodine atom is introduced by an I/*I exchange reaction.