161388-91-6

Basic information

• Product Name: 9-(2-Deoxy-β-D-erythro-pentofuranosyl)-6-O-(diphenylcarbamoyl)-2-N-isobutyrylguanine
• Synonyms: 9-(2-Deoxy-β-D-erythro-pentofuranosyl)-6-O-(diphenylcarbamoyl)-2-N-isobutyrylguanine
• CAS NO: 161388-91-6
• Molecular Weight: 532.556
• Mol File: 161388-91-6.mol
• Article Data: 2

Chemical Properties

• CAS DataBase Reference: 9-(2-Deoxy-β-D-erythro-pentofuranosyl)-6-O-(diphenylcarbamoyl)-2-N-isobutyrylguanine(CAS DataBase Reference)
• NIST Chemistry Reference: 9-(2-Deoxy-β-D-erythro-pentofuranosyl)-6-O-(diphenylcarbamoyl)-2-N-isobutyrylguanine(161388-91-6)
• EPA Substance Registry System: 9-(2-Deoxy-β-D-erythro-pentofuranosyl)-6-O-(diphenylcarbamoyl)-2-N-isobutyrylguanine(161388-91-6)

Safety Data

• Hazardous Substances Data: 161388-91-6(Hazardous Substances Data)

Upstream product

• 68892-42-2 N-isobutyryl-2'-deoxyguanosine 
• 83-01-2 diphenylcarbamic chloride 
• 961-07-9 2'-deoxyguanosine 
• 68892-42-2 N-[6-Hydroxy-9-((2R,4S,5R)-4-hydroxy-5-hydroxymethyl-tetrahydro-furan-2-yl)-9H-purin-2-yl]-isobutyramide 

Downstream Products

• 166758-20-9 9-(5-O-(N-Phthalimidyl)-2-deoxy-β-D-erythro-pentofuranosyl)-6-O-(diphenylcarbamoyl)-2-N-isobutyrylguanine 
• 190849-99-1 Carbonic acid (2R,3S,5R)-5-(6-diphenylcarbamoyloxy-2-isobutyrylamino-purin-9-yl)-3-hydroxy-tetrahydro-furan-2-ylmethyl ester 1-(6-nitro-benzo[1,3]dioxol-5-yl)-ethyl ester 
• 630109-94-3 Carbonic acid (2R,3S,5R)-5-(6-diphenylcarbamoyloxy-2-isobutyrylamino-purin-9-yl)-3-hydroxy-tetrahydro-furan-2-ylmethyl ester 3-trifluoromethyl-phenyl ester 

Relevant articles and documents

Solid-Phase Oligodeoxynucleotide Synthesis: A Two-Step Cycle Using Peroxy Anion Deprotection

A novel solid-phase phosphoramidite based oligodeoxynucleotide two-step synthesis method has been developed. Keys to this method are replacement of the 5′-dimethoxytrityl blocking group with an aryloxycarbonyl and the use of N-dimethoxytrityl protection for the exocyclic amines of adenine and cytosine. With these modifications, coupling of each 2′-deoxynucleoside 3′-phosphoramidite to the growing oligodeoxynucleotide on the solid support can be followed by treatment with an aqueous mixture of peroxy anions buffered at pH 9.6. This reagent effectively removes the carbonate protecting group and simultaneously oxidizes the phosphite internucleotide linkage. As a consequence a new two-step synthesis cycle is possible. Oligodeoxynucleotides synthesized using this approach are identical to authentic samples when tested by a variety of analytical techniques.