172405-18-4

Basic information

• Product Name: 9H-Purine-9-acetic acid, 6-[(4-methoxybenzoyl)amino]-
• CAS NO: 172405-18-4
• Molecular Formula: C15H13N5O4
• Molecular Weight: 327.299
• Mol File: 172405-18-4.mol
• Article Data: 4

Chemical Properties

• CAS DataBase Reference: 9H-Purine-9-acetic acid, 6-[(4-methoxybenzoyl)amino]-(CAS DataBase Reference)
• NIST Chemistry Reference: 9H-Purine-9-acetic acid, 6-[(4-methoxybenzoyl)amino]-(172405-18-4)
• EPA Substance Registry System: 9H-Purine-9-acetic acid, 6-[(4-methoxybenzoyl)amino]-(172405-18-4)

Safety Data

• Hazardous Substances Data: 172405-18-4(Hazardous Substances Data)

Upstream product

• 66224-66-6 adenine 
• 100-07-2 4-methoxy-benzoyl chloride 
• 25477-96-7 ethyl 2-(9H-adenin-9-yl)acetate 
• 97025-97-3 N⁶-(4-methoxybenzoyl) adenine 
• 312613-60-8 [6-(4-methoxy-benzoylamino)-purin-9-yl]-acetic acid tert-butyl ester 
• 172405-17-3 N⁶-(4-methoxybenzoyl)-9-(methoxycarbonylmethyl)adenine 

Downstream Products

• 864288-98-2 ([2-(4,5-dimethoxy-2-nitro-benzyloxycarbonylamino)-ethyl]-{[6-(4-methoxy-benzoylamino)-purin-9-yl]-acetyl}-amino)-acetic acid tert-butyl ester 
• 673458-62-3 N-(2,5-dihydroxycyclopentyl)-2-(N⁶-(p-methoxybenzoyl)adenin-1-yl)acetamide 
• 263254-51-9 ([2-(9H-Fluoren-9-ylmethoxycarbonylamino)ethyl]-{2-[6-(4-methoxybenzoylamino)purin-9-yl]acetyl}amino)acetic acid tert-butyl ester 
• 188779-59-1 ((2-tert-Butoxycarbonylamino-ethyl)-{2-[6-(4-methoxy-benzoylamino)-purin-9-yl]-acetyl}-amino)-acetic acid tert-butyl ester 
• 188779-53-5 ((2-Hydroxy-ethyl)-{2-[6-(4-methoxy-benzoylamino)-purin-9-yl]-acetyl}-amino)-acetic acid tert-butyl ester 
• 172405-39-9 methyl N-<2-((4-methoxyphenyl)-diphenylmethylamino)ethyl>-N-<(N⁶-(4-methoxybenzoyl)-adenin-9-yl)acetyl> glycinate 

Relevant articles and documents

Utilization of a combination of weak hydrogen-bonding interactions and phase segregation to yield highly thermosensitive supramolecular polymers

Supramolecular polymerization, i.e., the self-assembly of polymer-like materials through the utilization of the noncovalent bond, is a developing area of research. In this paper, we report the synthesis and investigation of nucleobase-terminated (N6

Substituted N-ethylglycine derivatives for preparing PNA and PNA/DNA hybrids

There are described N-ethylglycine derivatives of the formula I in which PG is a urethane-type or trityl-type amino protective group which is labile to weak acids, X is NH, O or S, Y is CH2, NH or O, and B' are bases customary in nucleotide chemistry, the exocyclic amino or hydroxyl groups of which being protected by suitable, known protective groups, or are base substitute compounds, and their salts with tert-organic bases, as well as a process for their preparation. The N-ethylglycine derivatives of the formula I are used in the preparation of PNA and PNA/DNA hybrids.