Coupling Reagents for DNA Synthesis

Application (±)-&#945:-Methoxyphenylacetic acid can be used as a reactant to synthesize:&nbsp:&nbsp:&nbsp:&nbsp:&nbsp:&nbsp: N -(Cyclohexylmethyl)-2-methoxy-2-phenylethylamine by reacting with cyclohexylmethylamine in the presence

Application (±)-&#945:-Methoxyphenylacetic acid can be used as a reactant to synthesize:&nbsp:&nbsp:&nbsp:&nbsp:&nbsp:&nbsp: N -(Cyclohexylmethyl)-2-methoxy-2-phenylethylamine by reacting with cyclohexylmethylamine in the presence

Application (±)-&#945:-Methoxyphenylacetic acid can be used as a reactant to synthesize:&nbsp:&nbsp:&nbsp:&nbsp:&nbsp:&nbsp: N -(Cyclohexylmethyl)-2-methoxy-2-phenylethylamine by reacting with cyclohexylmethylamine in the presence

Synonyms: for resolution of racemates Hill Formula: C₁₀H₁₆O₄S CAS Number: 3144-16-9 UN Number: UN3261

(4-Bromophenylethynyl)trimethylsilane can be synthesized by the palladium catalyzed reaction between 4-bromo-1-iodobenzene and trimethylsilylacetylene. It undergoes Buchwald-Hartwig coupling with para -substituted diphenylamines.

(4-Bromophenylethynyl)trimethylsilane can be synthesized by the palladium catalyzed reaction between 4-bromo-1-iodobenzene and trimethylsilylacetylene. It undergoes Buchwald-Hartwig coupling with para -substituted diphenylamines.

Application：Reactant for synthesis of:Cyclic guanidinesFive membered heterometallacycloallenesBenzimidazoles or quinazolines via nucleophilic addition and intramolecular C-C bond formationBenzoxazole and benzimidazole derivatives via cross-coupling

1-Ethyl-4-ethynylbenzene undergoes homocoupling reaction in the presence of copper chloride (catalyst) and air (oxidant) to yield symmetrical 1,4-disubstituted 1,3-diyne.

1-Ethyl-4-ethynylbenzene undergoes homocoupling reaction in the presence of copper chloride (catalyst) and air (oxidant) to yield symmetrical 1,4-disubstituted 1,3-diyne.

1-Ethyl-4-ethynylbenzene undergoes homocoupling reaction in the presence of copper chloride (catalyst) and air (oxidant) to yield symmetrical 1,4-disubstituted 1,3-diyne.

1-Ethyl-4-ethynylbenzene undergoes homocoupling reaction in the presence of copper chloride (catalyst) and air (oxidant) to yield symmetrical 1,4-disubstituted 1,3-diyne.

1-Ethyl-4-ethynylbenzene undergoes homocoupling reaction in the presence of copper chloride (catalyst) and air (oxidant) to yield symmetrical 1,4-disubstituted 1,3-diyne.