172405-09-3

Basic information

• Product Name: N⁴-(4-methoxybenzoyl)-1-(methoxycarbonylmethyl)cytosine
• Synonyms: N⁴-(4-methoxybenzoyl)-1-(methoxycarbonylmethyl)cytosine
• CAS NO: 172405-09-3
• Molecular Weight: 317.301
• Mol File: 172405-09-3.mol
• Article Data: 2

Chemical Properties

• CAS DataBase Reference: N⁴-(4-methoxybenzoyl)-1-(methoxycarbonylmethyl)cytosine(CAS DataBase Reference)
• NIST Chemistry Reference: N⁴-(4-methoxybenzoyl)-1-(methoxycarbonylmethyl)cytosine(172405-09-3)
• EPA Substance Registry System: N⁴-(4-methoxybenzoyl)-1-(methoxycarbonylmethyl)cytosine(172405-09-3)

Safety Data

• Hazardous Substances Data: 172405-09-3(Hazardous Substances Data)

Upstream product

• 100-07-2 4-methoxy-benzoyl chloride 
• 96-32-2 bromoacetic acid methyl ester 
• 51820-70-3 N₄-(4-methoxybenzoyl)-cytosine 

Downstream Products

• 864288-96-0 ([2-(4,5-dimethoxy-2-nitro-benzyloxycarbonylamino)-ethyl]-{[4-(4-methoxy-benzoylamino)-2-oxo-2H-pyrimidin-1-yl]-acetyl}-amino)-acetic acid tert-butyl ester 
• 172405-10-6 [4-(4-Methoxybenzoylamino)-2-oxo-1,2-dihydropyrimidin-1-yl]acetic acid 

Relevant articles and documents

Synthesis of photolabile o-nitroveratryloxycarbonyl (NVOC) protected peptide nucleic acid monomers

The chemical synthesis of peptide nucleic acid (PNA) monomers was accomplished using various combinations of the o-nitroveratryloxycarbonyl (NVOC) group (N-aminoethylglycine backbone) and base labile acyl-type nucleobase protecting groups (anisoyl for ade