516-12-1(N-Iodosuccinimide) Product Description

1-iodo-5-pyrrolidinedione N-IODOSUCCINIMIDE N-Iodosuccinimide, 98+% N-Iodosuccinimide ,99% N-Iodosuccinimide , (1-Iodo-2,5-pyrrolidinedione) 1-Iodopyrrolidine-2,5-dione, 2,5-Dioxo-1-iodopyrrolidine N-IodosucciniMide, 98% 100GR N-IodosucciniMide, 98% 10GR N-iodobutanimide/NIS N-IodosucciniMide / N-IodobutaniMide N-iodoDing twoiMide N - butyl diiMide iodine generation N-Iodosuccinimide 2,5-Pyrrolidinedione, 1-iodo- N-Iodosuccinimide, 97+% n-iodo-succinimid Succinimide,N-iodo- succiniodimide N-Iodosuccinimide≥ 99.9% (Iodometry) N-Iodosuccinimide, 97%, for synthesis N-Iodosuccinimide> N-IODOSUCCINIMIDE FOR SYNTHESIS N-succinimide (NIS) N-iododiimide N-iodosuccinimideb Big Discount Purity 99% N-Iodosuccinimide CAS 516-12-1 with Best Quality Intermediate Material N-Iodosuccinimide (NIS) CAS?516-12-1 N-Iodosuccinimide 5GM N-Iodosuccinimide extrapure, 99% IODOSUCCINIMIDE For Synthesis 1-IODO-2,5-PYRROLIDINEDIONE NIS N-IodosucciniMide (NIS) 1-iodopyrrolidine-2,5-dione Iodosuccinimide N-lodosuccinimide Ripretinib Impurity 39 N-Iodosuccinimide (1-Iodopyrrolidine-2,5-Dione) 516-12-1 208-221-6 512-12-1 C4H4INO2 C4H4O2NI Reagents for Oligosaccharide Synthesis Iodination N-Substituted Succinimides N-Substituted Maleimides, Succinimides & Phthalimides Halogenation C-X Bond Formation (Halogen) Synthetic Reagents C-X Bond Formation (Halogen) Synthetic Reagents Aromatic Carboxylic Acids, Amides, Anilides, Anhydrides & Salts API intermediates Biochemistry Halogenation Iodination N-Substituted Maleimides, Succinimides & Phthalimides