85070-63-9

Upstream product

• 4101-68-2 1,10-dibromodecane 
• 112999-97-0 2-[(12-bromododecyl)oxy]tetrahydro-2H-pyran 
• 502929-61-5 12-phenyldodecyl tetrahydropyranyl ether 
• 536-74-3 phenylacetylene 
• 3344-70-5 1,12-dibromododecane 
• 100-58-3 phenylmagnesium bromide 
• 85070-62-8 12-bromo-1-phenyl-dodec-1-yne 
• 88336-80-5 12-phenyl-1-dodecanol 

Downstream Products

• 116754-61-1 2-Methyl-14-phenyl-tetradecanoic acid 
• 116754-72-4 Toluene-4-sulfonic acid 2-methyl-14-phenyl-tetradecyl ester 
• 116754-65-5 2-Methyl-14-phenyl-tetradecanoic acid methyl ester 
• 116754-75-7 14-phenyl-2(RS)-methyltetradecanenitrile 
• 116754-69-9 14-phenyl-2(RS)-methyltetradecan-1-ol 
• 88336-88-3 Methyl 15-Phenyl-3(R,S)-methylpentadecanoate 
• 116754-80-4 15-Phenyl-3(R,S)-methylpentadecanoic Acid 
• 101948-01-0 N,N-dimethyl-1-(12-phenyldodecyl)-2,4-dimethyl-3-carbamoyl pyridinium bromide 
• 105419-04-3 O-dimethyl-4-(12'-phenyldodecyl)catechol 
• 105419-06-5 3-(12'-phenyldodecyl)veratrole 
• 95690-71-4 3-(12'-phenyldodecyl)benzene-1,2-diol 
• 95690-69-0 4-(12'-phenyldodecyl)benzene-1,2-diol 
• 101948-07-6 N,N-dimethyl-1-(12-phenyldodecyl)-2,4-dimethyl-3-carbamoyl-1,6-dihydropyridine 

Relevant academic research and scientific papers

2,2-Dichloroalkanecarboxylic acids, processes for their production and pharmaceutical agents containing these

Pharmaceutical agents for treating diabetus mellitus which contain a compound of formula I STR1 as the active substance, in which A, B, A' and W have the meanings stated in the claims, new compounds of formula I as well as processes for their production.

ω-Substituted alkyl carboxylic acids as antidiabetic and lipid-lowering agents

In screening experiments certain ω-substituted alkyl carboxylic acids were found to produce an increase in insulin-stimulated 14C-acetate incorporation into triglycerides, which may indicate an improvement in the action of insulin. Antidiabetic

Synthesis of 3- and 4-(ω-Phenylalkyl)catechols, the Sap Exuded from a Burmese Lac Tree, Melanorrhoea Usitate

The presence of 3- and 4-(ω-phenylalkyl)catechols in Burmese lac has been confirmed by their synthesis. 3-(ω-Phenylalkyl)veratroles were synthesized by alkylation of ω-phenylalkyl bromide with aryl lithium derived from veratrole. 4-(ω-phenylalkyl)veratroles were similarly obtained from w-phenylalkyl bromide and 4-bromoveratrole.Demethylation of 3- and 4-(ω-phenylalkyl)veratroles with boron tribromide gave the corresponding catechols in good yields.

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.