56577-39-0

Basic information

• Product Name: N⁴-phenoxyacetyl-2'-deoxycytidine
• CAS NO: 56577-39-0
• Molecular Weight: 361.354
• Mol File: 56577-39-0.mol

Chemical Properties

• CAS DataBase Reference: N⁴-phenoxyacetyl-2'-deoxycytidine(CAS DataBase Reference)
• NIST Chemistry Reference: N⁴-phenoxyacetyl-2'-deoxycytidine(56577-39-0)
• EPA Substance Registry System: N⁴-phenoxyacetyl-2'-deoxycytidine(56577-39-0)

Safety Data

• Hazardous Substances Data: 56577-39-0(Hazardous Substances Data)

Upstream product

• 122-59-8 2-phenoxyacetic acid 
• 951-77-9 2'-Deoxycytidine 
• 51432-42-9 4-Amino-1-((2R,4S,5R)-4-trimethylsilanyloxy-5-trimethylsilanyloxymethyl-tetrahydro-furan-2-yl)-1H-pyrimidin-2-one 
• 110009-60-4 1-(phenoxyacetyl)-1H-imidazole 
• 701-99-5 Phenoxyacetyl chloride 

Downstream Products

• 118533-21-4 5'-O-(4,4'-dimethoxytrityl)-N⁴-(phenoxyacetyl)-2'-deoxycytidine-3'-O-succinate 
• 118533-20-3 5'-O-(4,4'-dimethoxytrityl)-N⁴-phenoxyacetyl-2'-deoxycytidine 

Relevant articles and documents

A simple method for N-acylation of adenosine and cytidine nucleosides using carboxylic acids activated in-situ with carbonyldiimidazole

Carboxylic acids are activated with 1,1'-carbonyldiimidazole in acetonitrile to form N-acylimidazoles which are then treated with per-trimethylsilyl ethers of nucleosides adenosine or cytidine at ambient temperature to generate exclusively N-acylated-Aden

Improvements in Oligodeoxyribonucleotide Synthesis using Phenoxyacetyl as Amino Protecting Group

Phenoxyacetyl group has been used successfully for the protection of exocyclic amino function on purine and pyrimidine bases of 2'-deoxynucleosides.In the case of 2'-deoxycytidine, quantitative selective protection has been achieved under controlled condi