Iodoform

Iodotyrosine coupled with di-iodotyrosine results in the synthesis of 3,5,3&#8242-tri-iodothyronine (T3) or 3,3&#8242,5&#8242-tri-iodothyronine (rT3). Application 3-Iodo-L-tyrosine has been used as an inhibitor for tyrosine hydroxylase enzyme in

Iodotyrosine coupled with di-iodotyrosine results in the synthesis of 3,5,3&#8242-tri-iodothyronine (T3) or 3,3&#8242,5&#8242-tri-iodothyronine (rT3). Application 3-Iodo-L-tyrosine has been used as an inhibitor for tyrosine hydroxylase enzyme in

Iodotyrosine coupled with di-iodotyrosine results in the synthesis of 3,5,3&#8242-tri-iodothyronine (T3) or 3,3&#8242,5&#8242-tri-iodothyronine (rT3). Application 3-Iodo-L-tyrosine has been used as an inhibitor for tyrosine hydroxylase enzyme in

Other Notes Please note that Sigma-Aldrich provides this product to early discovery researchers as part of a collection of rare and unique chemicals. Sigma-Aldrich does not collect analytical data for this product.

Other Notes Please note that Sigma-Aldrich provides this product to early discovery researchers as part of a collection of rare and unique chemicals. Sigma-Aldrich does not collect analytical data for this product.

3-Iodoanisole

3-Iodoanisole

3-Iodoanisole

3-Iodobenzylamine

3-Iodobenzylamine

3-Iodooxetane

Application Reactant involved in: Aerobic oxidative coupling with arenes Coupling with acetals Synthesis of inhibitors of homoserine transacetylase Boron-Heck arylation with alkenes N- arylation Heck reactions with electrophilic alkenes Other Notes