Dinoprost trometamol

N-Succinimidyloxycarbonylmethyl tris(2,4,6-trimethoxyphenyl)phosphonium bromide (TMPP-Ac-OSu) is an acylating reagent, and is generally used for the selective derivatization of N-terminal a-amino group of peptide. The TMPP-acetylated peptides

(R)-(-)-2-Amino-1-propanol

(R)-(-)-2-Amino-1-propanol

Product Describtion:BOP coupling agent analogue, does not produce carcinogenic by-product HMPAProduct Application:Reagent for:Synthesis of single labeled oligonucleotides that fluoresce upon matched hybridizationGeneration of endocrine disruptor

Product Describtion:BOP coupling agent analogue, does not produce carcinogenic by-product HMPAProduct Application:Reagent for:Synthesis of single labeled oligonucleotides that fluoresce upon matched hybridizationGeneration of endocrine disruptor

Product Describtion:BOP coupling agent analogue, does not produce carcinogenic by-product HMPAProduct Application:Reagent for:Synthesis of single labeled oligonucleotides that fluoresce upon matched hybridizationGeneration of endocrine disruptor

Product Describtion:BOP coupling agent analogue, does not produce carcinogenic by-product HMPAProduct Application:Reagent for:Synthesis of single labeled oligonucleotides that fluoresce upon matched hybridizationGeneration of endocrine disruptor

Product Describtion:BOP coupling agent analogue, does not produce carcinogenic by-product HMPAProduct Application:Reagent for:Synthesis of single labeled oligonucleotides that fluoresce upon matched hybridizationGeneration of endocrine disruptor

Application 2,6-Difluoroaniline was used in the synthesis of: N -2,6-difluorophenyl-5-methoxy-1,2,4-triazolo[1,5- a ]pyrimidine-2-sulfonamide, herbicidal compound series of 2,6,9-trisubstituted purine inhibitors of p38&#945 kinase substituted

Application 2-Cyanoethyl N,N -diisopropylchlorophosphoramidite was employed: for selective monophosphorylation of carbohydrates and nucleosides for conversion of protected ribonucleosides to phosphoramidites as phosphitylating reagent for

Application 2-Cyanoethyl N,N -diisopropylchlorophosphoramidite was employed: for selective monophosphorylation of carbohydrates and nucleosides for conversion of protected ribonucleosides to phosphoramidites as phosphitylating reagent for

Application 2-Cyanoethyl N,N -diisopropylchlorophosphoramidite was employed: for selective monophosphorylation of carbohydrates and nucleosides for conversion of protected ribonucleosides to phosphoramidites as phosphitylating reagent for