299916-67-9

Basic information

• Product Name: 4H-1,3-Dioxolo4,5-cpyrrole-4-methanol, tetrahydro-6-4-methoxy-5-(phenylmethoxy)methyl-5H-pyrrolo3,2-dpyrimidin-7-yl-2,2-dimethyl-, (3aR,4R,6S,6aS)-
• Synonyms: 4H-1,3-Dioxolo4,5-cpyrrole-4-methanol, tetrahydro-6-4-methoxy-5-(phenylmethoxy)methyl-5H-pyrrolo3,2-dpyrimidin-7-yl-2,2-dimethyl-, (3aR,4R,6S,6aS)-;(1S)-1-(7-N-benzyloxyMethyl-9-deaza-6-O-Methylhypoxanthin-9-yl)-1,4-dideoxy-1,4-iMino-2,3-O-isopropylidene-D-ribitol
• CAS NO: 299916-67-9
• Molecular Formula: C₂₃H₂₈N₄O₅
• Molecular Weight: 440.49
• Mol File: 299916-67-9.mol
• Article Data: 3

Chemical Properties

• Appearance: /
• CAS DataBase Reference: 4H-1,3-Dioxolo4,5-cpyrrole-4-methanol, tetrahydro-6-4-methoxy-5-(phenylmethoxy)methyl-5H-pyrrolo3,2-dpyrimidin-7-yl-2,2-dimethyl-, (3aR,4R,6S,6aS)-(CAS DataBase Reference)
• NIST Chemistry Reference: 4H-1,3-Dioxolo4,5-cpyrrole-4-methanol, tetrahydro-6-4-methoxy-5-(phenylmethoxy)methyl-5H-pyrrolo3,2-dpyrimidin-7-yl-2,2-dimethyl-, (3aR,4R,6S,6aS)-(299916-67-9)
• EPA Substance Registry System: 4H-1,3-Dioxolo4,5-cpyrrole-4-methanol, tetrahydro-6-4-methoxy-5-(phenylmethoxy)methyl-5H-pyrrolo3,2-dpyrimidin-7-yl-2,2-dimethyl-, (3aR,4R,6S,6aS)-(299916-67-9)

Safety Data

• Hazardous Substances Data: 299916-67-9(Hazardous Substances Data)

Upstream product

• 1185908-34-2 C₂₃H₂₆N₄O₅ 
• 5655-01-6 9-deazahypoxanthine 
• 364046-18-4 1S-5-O-tert-butyldimethylsilyl-1,4-dideoxy-1-C-[(4-methyoxypyrrolo[3,2-d]pyrimidin-9-N-(benzyloxomethyl)-7-yl)]-1,4-imino-2,3-O-isopropylidine-D-ribitol 
• 299916-62-4 7-N-benzyloxymethyl-9-bromo-9-deaza-6-O-methylhypoxanthine 
• 1026012-16-7 5-(benzyloxymethyl)-4-methoxy-5H-pyrrolo[3,2-d]pyrimidine 
• 84905-80-6 4-Chloro-5H-pyrrolo[3,2-d]pyrimidine 

Downstream Products

• 209799-67-7 forodesine 

Relevant articles and documents

Alternative route towards the convergent synthesis of a human purine nucleoside phosphorylase inhibitor-forodesine HCl

Forodesine HCl is being investigated as a potential target for the control of T-cell proliferation. Herein we present an alternative route for the synthesis of the target molecule with addition of lactam to the lithiated deazahypoxanthine (generated in situ). The lactam was synthesized in five steps starting from l-pyroglutamic acid.

Addition of lithiated 9-deazapurine derivatives to a carbohydrate cyclic imine: Convergent synthesis of the aza-C-nucleoside immucillins

Means have been developed for the synthesis and addition of 9-deaza-9-lithiopurine derivatives to the carbohydrate-derived cyclic imine 6 in facile convergent syntheses of biologically active aza-C-nucleosides.