170871-03-1

Basic information

• Product Name: {3-[(2R,4S,5R)-4-(tert-Butyl-dimethyl-silanyloxy)-5-(tert-butyl-dimethyl-silanyloxymethyl)-tetrahydro-furan-2-yl]-5-carbamoyl-3H-imidazol-4-yl}-carbamic acid benzyl ester
• Synonyms: {3-[(2R,4S,5R)-4-(tert-Butyl-dimethyl-silanyloxy)-5-(tert-butyl-dimethyl-silanyloxymethyl)-tetrahydro-furan-2-yl]-5-carbamoyl-3H-imidazol-4-yl}-carbamic acid benzyl ester
• CAS NO: 170871-03-1
• Molecular Weight: 604.894
• Mol File: 170871-03-1.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: {3-[(2R,4S,5R)-4-(tert-Butyl-dimethyl-silanyloxy)-5-(tert-butyl-dimethyl-silanyloxymethyl)-tetrahydro-furan-2-yl]-5-carbamoyl-3H-imidazol-4-yl}-carbamic acid benzyl ester(CAS DataBase Reference)
• NIST Chemistry Reference: {3-[(2R,4S,5R)-4-(tert-Butyl-dimethyl-silanyloxy)-5-(tert-butyl-dimethyl-silanyloxymethyl)-tetrahydro-furan-2-yl]-5-carbamoyl-3H-imidazol-4-yl}-carbamic acid benzyl ester(170871-03-1)
• EPA Substance Registry System: {3-[(2R,4S,5R)-4-(tert-Butyl-dimethyl-silanyloxy)-5-(tert-butyl-dimethyl-silanyloxymethyl)-tetrahydro-furan-2-yl]-5-carbamoyl-3H-imidazol-4-yl}-carbamic acid benzyl ester(170871-03-1)

Safety Data

• Hazardous Substances Data: 170871-03-1(Hazardous Substances Data)

Upstream product

• 37642-56-1 5-Amino-1-(2'-deoxy-β-D-ribofuranosyl)imidazole-4-carboxamide 
• 18162-48-6 tert-butyldimethylsilyl chloride 
• 501-53-1 benzyl chloroformate 
• 170871-02-0 5-amino-1-(3,5-di-O-tert-butyldimethylsilyl-2-deoxy-β-D-ribofuranosyl)imidazole-4-carboxamide 

Downstream Products

• 170871-10-0 (3-{(2R,4S,5R)-5-[Bis-(4-methoxy-phenyl)-phenyl-methoxymethyl]-4-[(2-chloro-phenoxy)-(2-cyano-ethoxy)-phosphoryloxy]-tetrahydro-furan-2-yl}-5-carbamoyl-3H-imidazol-4-yl)-carbamic acid benzyl ester 
• 170871-08-6 5-(benzyloxycarbonyl)amino-1-(5-O-dimethoxytrityl-2-deoxy-β-D-ribofuranosyl)imidazole-4-carboxamide 
• 29049-22-7 2'-deoxyxanthosine 
• 170871-05-3 5-(benzyloxycarbonyl)amino-1-(2-deoxy-β-D-ribofuranosyl)imidazole-4-carboxamide 

Relevant articles and documents

Oligodeoxynucleotides embodying the ambiguous base Z, 5-amino-imidazole- 4-carboxamide

Short oligomers containing 5-amino-1-(2-deoxy-β-D- ribofuranosyl)imidazole -4-carboxamide (dZ) were synthesized in solution using the phosphotriester methodology. Usual acyl groups were used for the canonical bases. For the exocyclic amino function of Z residue, the hydrogenolyzable benzyloxycarbonyl group was introduced.