112233-75-7

Basic information

• Product Name: Guanosine, N-acetyl-, 2',3',5'-triacetate 6-(diphenylcarbamate)
• CAS NO: 112233-75-7
• Molecular Formula: C31H30N6O10
• Molecular Weight: 646.613
• Mol File: 112233-75-7.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: Guanosine, N-acetyl-, 2',3',5'-triacetate 6-(diphenylcarbamate)(CAS DataBase Reference)
• NIST Chemistry Reference: Guanosine, N-acetyl-, 2',3',5'-triacetate 6-(diphenylcarbamate)(112233-75-7)
• EPA Substance Registry System: Guanosine, N-acetyl-, 2',3',5'-triacetate 6-(diphenylcarbamate)(112233-75-7)

Safety Data

• Hazardous Substances Data: 112233-75-7(Hazardous Substances Data)

Usage

General Description

Guanosine, N-acetyl-, 2',3',5'-triacetate 6-(diphenylcarbamate) is a chemical compound that is a modified form of guanosine, a nucleoside involved in the construction of DNA and RNA. This specific derivative has three acetate groups attached to the 2', 3', and 5' hydroxyl groups of the guanosine molecule, as well as a diphenylcarbamate group. The addition of these groups alters the properties and function of the guanosine molecule, potentially affecting its role in cellular processes such as signaling, metabolism, and gene expression. Guanosine, N-acetyl-, 2',3',5'-triacetate 6-(diphenylcarbamate) may have applications in medicinal chemistry, biotechnology, and biochemical research due to its modified structure and potential biological activities.

Upstream product

• 112233-74-6 N₂-acetyl-O₆-(diphenylcarbamoyl)guanine 
• 13035-61-5 1,2,3,5-tetraacetylribose 
• 30747-23-0 Acetic acid (2R,3R,4R,5R)-4-acetoxy-5-acetoxymethyl-2-(2-acetylamino-6-oxo-1,6-dihydro-purin-9-yl)-tetrahydro-furan-3-yl ester 
• 83-01-2 diphenylcarbamic chloride 
• 185610-61-1 Acetic acid (2R,3R,4R,5R)-4-acetoxy-5-acetoxymethyl-2-(2-acetylamino-6-diphenylcarbamoyloxy-purin-7-yl)-tetrahydro-furan-3-yl ester 
• 3056-33-5 2,9-diacetylguanine 
• 73-40-5 2-amino-1,9-dihydro-6H-purin-6-one 
• 118-00-3 G 

Downstream Products

• 118-00-3 G 
• 1092359-47-1 2-[acetyl(2-bromobenzyl)amino]-6-(diphenylcarbamoyloxy)-9-(β-D-tri-O-acetylribofuranosyl)-9H-purine 
• 30747-23-0 Acetic acid (2R,3R,4R,5R)-4-acetoxy-5-acetoxymethyl-2-(2-acetylamino-6-oxo-1,6-dihydro-purin-9-yl)-tetrahydro-furan-3-yl ester 

Relevant articles and documents

The determinative influence of the O6-(diphenylcarbamoyl) group on the exocyclic nitrogen benzylation in 2-amino-6-oxopurine derivatives

A series of novel 2-(benzylamino)-6-oxopurine derivatives has been synthesized by arylalkylation of the corresponding 2-(acetylamino)-6- (diphenylcarbamoyloxy)purines. The decisive role of the temporary O 6-(diphenylcarbamoyl) protection on the benzylation of the exocyclic amino group in 2-(acetylamino)-6-oxopurines has been demonstrated. Georg Thieme Verlag Stuttgart.

High-yield regioselective synthesis of 9-glycosyl guanine nucleosides and analogues via coupling with 2-N-acetyl-6-O-diphenylcarbamoylguanine

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