Controlled substance analgesic amides and amines

phenylacetyl-Arg-Val-Arg-4-amidinobenzylamide.

Application PhPAd-DalPhos Ni( o -tolyl)Cl is an air stable precatalyst developed in the Stradiotto lab used for coupling of bulky primary amines with arenes. Other Notes Technology Spotlight: DalPhos ligands PhPAd-DalPhos: Ligand-Enabled,

Phthalamic acid can be synthesized from the reaction between ammonia and phthalic anhydride by a modified Auger′s method. Kinetic studies of the intramolecular carboxylic-group assisted hydrolysis of amide bond of phthalamic acid provided the value

Phthalamic acid can be synthesized from the reaction between ammonia and phthalic anhydride by a modified Auger′s method. Kinetic studies of the intramolecular carboxylic-group assisted hydrolysis of amide bond of phthalamic acid provided the value

Phthalamic acid can be synthesized from the reaction between ammonia and phthalic anhydride by a modified Auger′s method. Kinetic studies of the intramolecular carboxylic-group assisted hydrolysis of amide bond of phthalamic acid provided the value

Phthalamic acid can be synthesized from the reaction between ammonia and phthalic anhydride by a modified Auger′s method. Kinetic studies of the intramolecular carboxylic-group assisted hydrolysis of amide bond of phthalamic acid provided the value

Poly(ethylene glycol) bis(amine).

Poly(ethylene glycol) bis(amine).

Poly(ethylene glycol) bis(amine).

DescriptionPolymer architecture: DendronEnd Group Functionality: Boc-protected amineBoc :tert-ButyloxycarbonylBis-MPA : 2,2-Bis(hydroxymethyl)propionic acidBis-MPA (or 2,2-Bis(methylol)propionic acid) is an aliphatic, pro-chiral molecule comprised

Descriptioncalculated mol. wt. 1878.9Amine dendrons can be covalently attached through conjugation to carboxyl groups, primary amines, or sulfhydryl groups. Amines can also attach to oxidized carbohydrate groups (usually aldehydes) by reductive

Descriptioncalculated mol. wt. 259.3Azide dendrons can be coupled to acetylene functionalized molecules, including acetylene dendrons to form asymmetric dendrimers.