174221-87-5

Basic information

• Product Name: Cytidine, 2'-amino-5'-O-[bis(4-methoxyphenyl)phenylmethyl]-2'-deoxy-
• CAS NO: 174221-87-5
• Molecular Formula: C30H32N4O6
• Molecular Weight: 544.607
• Mol File: 174221-87-5.mol
• Article Data: 2

Chemical Properties

• CAS DataBase Reference: Cytidine, 2'-amino-5'-O-[bis(4-methoxyphenyl)phenylmethyl]-2'-deoxy-(CAS DataBase Reference)
• NIST Chemistry Reference: Cytidine, 2'-amino-5'-O-[bis(4-methoxyphenyl)phenylmethyl]-2'-deoxy-(174221-87-5)
• EPA Substance Registry System: Cytidine, 2'-amino-5'-O-[bis(4-methoxyphenyl)phenylmethyl]-2'-deoxy-(174221-87-5)

Safety Data

• Hazardous Substances Data: 174221-87-5(Hazardous Substances Data)

Upstream product

• 213487-23-1 2'-azido-5'-O-(4,4'-dimethoxytrityl)-2'-deoxycytidine 
• 58-96-8 uridine 
• 174221-83-1 1-{(3aR,4R,6R,6aS)-6-[Bis-(4-methoxy-phenyl)-phenyl-methoxymethyl]-2-trichloromethyl-3a,4,6,6a-tetrahydro-furo[3,4-d]oxazol-4-yl}-4-[1,2,4]triazol-1-yl-1H-pyrimidin-2-one 
• 174221-82-0 5'-O-(4,4'-dimethoxytrityl)-2'-N,3'-O-(2-(trichloromethyl)oxazolino)-2'-deoxy-1-(β-D-ribofuranosyl)uracil 
• 173170-12-2 2,2'-O-anhydro-1-<5'-O-(4,4'-dimethoxytrityl)-β-D-arabinofuranosyl>uracil 
• 3736-77-4 2,2'-Anhydrouridine 
• 807370-67-8 1-{(2R,3R,4S,5R)-3-Azido-5-[bis-(4-methoxy-phenyl)-phenyl-methoxymethyl]-4-trimethylsilanyloxy-tetrahydro-furan-2-yl}-4-[1,2,4]triazol-1-yl-1H-pyrimidin-2-one 
• 807370-61-2 2'-azido-5'-O-(4,4'-dimethoxytrityl)-3'-O-trimethylsilyl-2'-deoxyuridine 
• 26929-65-7 2'-azido-2'-deoxyuridine 
• 177980-10-8 2'-azido-5'-O-(4,4'-dimethoxytrityl)-2'-deoxyuridine 
• 40615-36-9 4,4'-dimethoxytrityl chloride 
• 174221-84-2 5'-O-(4,4'-dimethoxytrityl)-2'-N,3'-O-(2-(trichloromethyl)oxazolino)-2'-deoxycytidine 

Downstream Products

• 807370-92-9 N⁴-benzoyl-5'-O-(4,4'-dimethoxytrityl)-2'-methoxyoxalylamino-2'-deoxycytidine 
• 174221-88-6 5'-O-(4,4'-dimethoxytrityl)-2'-trifluoroacetamido-2'-deoxycytidine 

Relevant articles and documents

Monomers for oligonucleotide synthesis with linkers carrying reactive residues: II. The synthesis of phosphoamidites on the basis of uridine and cytosine and containing a linker with methoxyoxalamide groups in position 2′

A convenient preparative synthesis of 2′-amino-2′-deoxyuridine was developed. Starting from 2′-amino-2′-deoxyuridine and 2′-amino-2′-deoxycytidine, monomers for the phosphoamidite oligonucleotide synthesis were obtained that carry a linker with methoxyoxalamide groups in position 2′.