199938-73-3

Basic information

• Product Name: chloro-7-[2-deoxy-3,5-di-O-(4-toluoyl)-β-D-erythro-pentofuranosyl]-5-iodo-2-pivaloylamino-7H-pyrrolo[2,3-d]pyrimidine
• Synonyms: chloro-7-[2-deoxy-3,5-di-O-(4-toluoyl)-β-D-erythro-pentofuranosyl]-5-iodo-2-pivaloylamino-7H-pyrrolo[2,3-d]pyrimidine
• CAS NO: 199938-73-3
• Molecular Weight: 730.987
• Mol File: 199938-73-3.mol
• Article Data: 4

Chemical Properties

• CAS DataBase Reference: chloro-7-[2-deoxy-3,5-di-O-(4-toluoyl)-β-D-erythro-pentofuranosyl]-5-iodo-2-pivaloylamino-7H-pyrrolo[2,3-d]pyrimidine(CAS DataBase Reference)
• NIST Chemistry Reference: chloro-7-[2-deoxy-3,5-di-O-(4-toluoyl)-β-D-erythro-pentofuranosyl]-5-iodo-2-pivaloylamino-7H-pyrrolo[2,3-d]pyrimidine(199938-73-3)
• EPA Substance Registry System: chloro-7-[2-deoxy-3,5-di-O-(4-toluoyl)-β-D-erythro-pentofuranosyl]-5-iodo-2-pivaloylamino-7H-pyrrolo[2,3-d]pyrimidine(199938-73-3)

Safety Data

• Hazardous Substances Data: 199938-73-3(Hazardous Substances Data)

Upstream product

• 104291-20-5 (2R,3S,5R)-5-(2-amino-4-chloro-7H-pyrrolo[2,3-d]pyrimidin-7-yl)-2-(((4-methylbenzoyl)oxy)methyl)tetrahydrofuran-3-yl 4-methylbenzoate 
• 3282-30-2 pivaloyl chloride 
• 149765-15-1 N-(4-chloro-7H-pyrrolo[2,3-d]pyrimidin-2-yl)-2,2-dimethyl-propionamide 
• 84955-31-7 4-chloro-7H-pyrrolo[2,3-d]pyrimidin-2-amine 
• 3601-89-6 Hoffer's chlorosugar 
• 149765-16-2 N-(4-chloro-5-iodo-7H-pyrrolo[2,3-d]pyrimidin-2-yl)-2,2-dimethyl-propionamide 
• 4330-21-6 2-deoxy-3,5-di-O-p-toluoyl-α-D-erythro-pentofuranosyl chloride 

Downstream Products

• 213823-27-9 C₄₉H₄₃N₅O₇ 
• 213823-23-5 C₄₆H₄₀IN₅O₇ 
• 213823-33-7 N-[7-{(2R,4S,5R)-5-[Bis-(4-methoxy-phenyl)-phenyl-methoxymethyl]-4-hydroxy-tetrahydro-furan-2-yl}-5-cyano-2-(2,2-dimethyl-propionylamino)-7H-pyrrolo[2,3-d]pyrimidin-4-yl]-2,2-dimethyl-propionamide 
• 213823-30-4 C₃₈H₄₂N₆O₇ 
• 199938-84-6 C₂₈H₂₅N₅O₅ 
• 199938-77-7 C₂₅H₂₂IN₅O₅ 

Relevant articles and documents

Nucleoside heterocycle that binds to both thymidine and cytidine

This application discloses nucleoside analogs that when incorporated into a oligonucleotide, forms a nucleobase pair with either thymidine or cytidine that are present in a complementary strand at the paired position. These analogs are called “purine bive

Regioselective syntheses of 7-halogenated 7-deazapurine nucleosides related to 2-amino-7-deaza-2′-deoxyadenosine and 7-deaza-2′- deoxyisoguanosine

The syntheses of 7-halogenated derivatives 3b-e of 2-amino-7-deaza- 2′-deoxyadenosine as well as 7-bromo and 7-chloro-7-deaza-2′- deoxyisoguanosines 4b-c are described. Nucleobase anion glycosylation was employed for the convergent nucleoside synthesis. T