73591-22-7

Basic information

• Product Name: 3'-Cytidylic acid,5'-O-[bis(4-methoxyphenyl)phenylmethyl]-P-(4-chlorophenyl)-2'-deoxy-N-(2-methyl-1-oxopropyl)guanylyl-(3'®5')-N-benzoyl-2'-deoxy-,4-chlorophenyl 2-cyanoethyl ester (9CI)
• CAS NO: 73591-22-7
• Molecular Formula: C66H63 Cl2 N9 O17 P2
• Molecular Weight: 1387.13
• Mol File: 73591-22-7.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: 3'-Cytidylic acid,5'-O-[bis(4-methoxyphenyl)phenylmethyl]-P-(4-chlorophenyl)-2'-deoxy-N-(2-methyl-1-oxopropyl)guanylyl-(3'®5')-N-benzoyl-2'-deoxy-,4-chlorophenyl 2-cyanoethyl ester (9CI)(CAS DataBase Reference)
• NIST Chemistry Reference: 3'-Cytidylic acid,5'-O-[bis(4-methoxyphenyl)phenylmethyl]-P-(4-chlorophenyl)-2'-deoxy-N-(2-methyl-1-oxopropyl)guanylyl-(3'®5')-N-benzoyl-2'-deoxy-,4-chlorophenyl 2-cyanoethyl ester (9CI)(73591-22-7)
• EPA Substance Registry System: 3'-Cytidylic acid,5'-O-[bis(4-methoxyphenyl)phenylmethyl]-P-(4-chlorophenyl)-2'-deoxy-N-(2-methyl-1-oxopropyl)guanylyl-(3'®5')-N-benzoyl-2'-deoxy-,4-chlorophenyl 2-cyanoethyl ester (9CI)(73591-22-7)

Safety Data

• Hazardous Substances Data: 73591-22-7(Hazardous Substances Data)

Upstream product

• 67219-55-0 4-N-Benzoyl-2'-deoxy-5'-O-(4,4'-dimethoxytrityl)cytidine 
• 62420-37-5 (p-chlorophenyl) di(1,2,4-triazolido)phosphate 
• 57777-87-4 N⁴-benzoyl-5'-O-(p,p'-dimethoxytrityl)deoxycytidine 3'-<(p-chlorophenyl)(β-cyanoethyl)phosphate> 
• 69507-62-6 (p-chlorophenyl) (β-cyanoethyl) phosphorochloridate 
• 68892-41-1 5'-O-dimethoxytrityl-N-isobutyryldeoxyguanosine 
• 71100-63-5 C₄₁H₄₀ClN₅O₁₀P^(1-) 
• 67473-53-4 dbzCp(ClPh,CNEt) 

Downstream Products

• 74930-93-1 C₄₅H₄₅Cl₂N₉O₁₅P₂ 

Relevant articles and documents

Synthesis of Deoxyoligonucleotide Linker Fragments for Genetic Engineering Using Improved Preparative and Analytical Techniques

For studies on the expression of recombinant DNA, linker fragments have been prepared which serve to introduce specific points of cleavage on the DNA as well as the protein level.Such linkers were designed for cyanogen bromide as well as for collagenase cleavage of fused proteins.The preparation was done according to the triester synthesis scheme using improved and simpler routes to functionalized dinucleotide building blocks.Field desorption mass spectrometry was used as a routine tool for the identification and control of the purity of these units.