243844-65-7

Basic information

• Product Name: O⁶-allyl-N²-[(allyloxy)carbonyl]-5'-O-(p,p'-dimethoxytrityl)-2'-O-(tert-butyldimethylsilyl)guanosine 3'-(allyl N,N'-diisorpopylphosphoramidite)
• Synonyms: O⁶-allyl-N²-[(allyloxy)carbonyl]-5'-O-(p,p'-dimethoxytrityl)-2'-O-(tert-butyldimethylsilyl)guanosine 3'-(allyl N,N'-diisorpopylphosphoramidite)
• CAS NO: 243844-65-7
• Molecular Weight: 1011.24
• Mol File: 243844-65-7.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: O⁶-allyl-N²-[(allyloxy)carbonyl]-5'-O-(p,p'-dimethoxytrityl)-2'-O-(tert-butyldimethylsilyl)guanosine 3'-(allyl N,N'-diisorpopylphosphoramidite)(CAS DataBase Reference)
• NIST Chemistry Reference: O⁶-allyl-N²-[(allyloxy)carbonyl]-5'-O-(p,p'-dimethoxytrityl)-2'-O-(tert-butyldimethylsilyl)guanosine 3'-(allyl N,N'-diisorpopylphosphoramidite)(243844-65-7)
• EPA Substance Registry System: O⁶-allyl-N²-[(allyloxy)carbonyl]-5'-O-(p,p'-dimethoxytrityl)-2'-O-(tert-butyldimethylsilyl)guanosine 3'-(allyl N,N'-diisorpopylphosphoramidite)(243844-65-7)

Safety Data

• Hazardous Substances Data: 243844-65-7(Hazardous Substances Data)

Upstream product

• 243844-61-3 O⁶-allyl-N²-[(allyloxy)carbonyl]-5'-O-(p,p'-dimethoxytrityl)guanosine 
• 243844-59-9 C₂₇H₃₁N₅O₁₂ 
• 40615-36-9 4,4'-dimethoxytrityl chloride 
• 108554-72-9 (allyloxy)bis(diisopropylamino)phosphine 
• 243844-62-4 O⁶-allyl-N²-[(allyloxy)carbonyl]-5'-O-(p,p'-dimethoxytrityl)-2'-O-(tert-butyldimethylsilyl)guanosine 
• 243844-60-2 O⁶-allyl-N²-[(allyloxy)carbonyl]guanosine 
• 243844-57-7 Acetic acid (2R,3R,4R,5R)-4-acetoxy-5-acetoxymethyl-2-(6-allyloxy-2-amino-purin-9-yl)-tetrahydro-furan-3-yl ester 
• 6979-94-8 2',3',5'-tri-O-acetyl-guanosine 

Relevant articles and documents

Improved methods for the preparation of 2'-deoxyribonucleoside and ribonucleoside 3'-phosphoramidites with allylic protectors

Improved methods of preparing 2'-deoxyribonucleoside and ribonucleoside 3'phosphoramidites with allylic protecting groups, which serve as useful building blocks, particularly for the synthesis of base-labile derivatives, are developed.