132076-57-4

Basic information

• Product Name: 5'-phospho-2'-deoxycytidylyl(3'-5')-3'-O-adenosine
• Synonyms: 5'-phospho-2'-deoxycytidylyl(3'-5')-3'-O-adenosine
• CAS NO: 132076-57-4
• Molecular Weight: 1022.77
• Mol File: 132076-57-4.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: 5'-phospho-2'-deoxycytidylyl(3'-5')-3'-O-adenosine(CAS DataBase Reference)
• NIST Chemistry Reference: 5'-phospho-2'-deoxycytidylyl(3'-5')-3'-O-adenosine(132076-57-4)
• EPA Substance Registry System: 5'-phospho-2'-deoxycytidylyl(3'-5')-3'-O-adenosine(132076-57-4)

Safety Data

• Hazardous Substances Data: 132076-57-4(Hazardous Substances Data)

Upstream product

• 30034-25-4 N-(4,5-dimethoxy-2-nitrobenzyloxycarbonyl)-L-phenylalanine 
• 42855-00-5 nitroveratryloxycarbonyl chloride 
• 63-91-2 L-phenylalanine 
• 127067-28-1 5'-O-phosphoryl-2'-deoxycytidylyl-(3'->5')adenosine 
• 132018-86-1 N-NVOC-L-phenylalanine cyanomethyl ester 

Relevant articles and documents

A general and efficient route for chemical aminoacylation of transfer RNAs

A general and expedient procedure for the synthesis of aminoaeyl tRNA has been developed. The preparation of aminoacyl dCpA in one step and in high yield by reaction of the cyanomethyl active esters of N-protected α-amino with pdCpA is detailed. The preparation and photodeprotection of aminoacyl pdCpA derivatives containing nitroveratryl (NVOC) N-protected amino acids is also studied. The utility of the above methods for preparing aminoacyl tRNA was confirmed by enzymatically ligating NVOC-phenylalanyl pdCpA to tRNA-COH followed by photolysis to provide unprotected phenylalanyl tRNA. The phenylalanyl tRNA shown to be competent in an in vitro protein biosynthesis system. These protocols greatly simplify the use of chemically misacylated tRNAs in the synthesis of proteins containing unnatural ainino acids, as well as in studies of protein biosynthesis.