284490-18-2

Basic information

• Product Name: 1,3,5,2,4-Trioxadisilocino7,6-bpyrrole-7(6H)-carboxylic acid, 8-(1Z)-1-cyano-2-hydroxyethenyltetrahydro-2,2,4,4-tetrakis(1-methylethyl)-, 1,1-dimethylethyl ester, (6aR,8R,9aS)-
• Synonyms: 1,3,5,2,4-Trioxadisilocino7,6-bpyrrole-7(6H)-carboxylic acid, 8-(1Z)-1-cyano-2-hydroxyethenyltetrahydro-2,2,4,4-tetrakis(1-methylethyl)-, 1,1-dimethylethyl ester, (6aR,8R,9aS)-
• CAS NO: 284490-18-2
• Molecular Formula: C25H46N2O6Si2
• Mol File: 284490-18-2.mol
• Article Data: 1

Chemical Properties

• Appearance: /
• CAS DataBase Reference: 1,3,5,2,4-Trioxadisilocino7,6-bpyrrole-7(6H)-carboxylic acid, 8-(1Z)-1-cyano-2-hydroxyethenyltetrahydro-2,2,4,4-tetrakis(1-methylethyl)-, 1,1-dimethylethyl ester, (6aR,8R,9aS)-(CAS DataBase Reference)
• NIST Chemistry Reference: 1,3,5,2,4-Trioxadisilocino7,6-bpyrrole-7(6H)-carboxylic acid, 8-(1Z)-1-cyano-2-hydroxyethenyltetrahydro-2,2,4,4-tetrakis(1-methylethyl)-, 1,1-dimethylethyl ester, (6aR,8R,9aS)-(284490-18-2)
• EPA Substance Registry System: 1,3,5,2,4-Trioxadisilocino7,6-bpyrrole-7(6H)-carboxylic acid, 8-(1Z)-1-cyano-2-hydroxyethenyltetrahydro-2,2,4,4-tetrakis(1-methylethyl)-, 1,1-dimethylethyl ester, (6aR,8R,9aS)-(284490-18-2)

Safety Data

• Hazardous Substances Data: 284490-18-2(Hazardous Substances Data)

Usage

Chemical structure

The compound consists of a siloxane ring and a pyrrole ring, as well as a carboxylic acid functional group.

Functional groups

Carboxylic acid, cyano, hydroxy, and ester groups are present in the molecule.

Stereochemistry

The compound has a specific configuration indicated by the (6aR,8R,9aS)notation, which describes the arrangement of atoms in three-dimensional space.

Substituents

The compound contains a tetrakis(1-methylethyl) group and a 1-cyano-2-hydroxyethenyl group.

Atom composition

The molecule is composed of carbon, hydrogen, oxygen, silicon, and nitrogen atoms.

Molecular complexity

The compound has a complex and long chemical name, indicating a high level of molecular complexity.

Potential applications

Due to its unique structure and functional groups, the compound may have diverse potential applications in fields such as pharmaceuticals, materials science, and chemical synthesis.

Solubility

The compound's solubility properties are not explicitly mentioned, but it may be soluble in organic solvents due to its nonpolar nature.

Stability

The stability of the compound under various conditions (e.g., temperature, pH, etc.) is not provided, but it may be sensitive to certain conditions due to the presence of functional groups.

Reactivity

The compound may exhibit reactivity with various reagents due to the presence of functional groups such as carboxylic acid, cyano, and hydroxy groups.
Please note that this list is based on the information provided and general knowledge of chemical properties. Further experimental data and analysis would be required to confirm these properties and explore the compound's potential applications.

Upstream product

• 222854-82-2 N-tert-butoxycarbonyl-2,3,6-trideoxy-4-O-[imidazole-(thiocarbonyl)]-3,6-imino-5,7-O-(1,1,3,3-tetraisopropyldisiloxa-1,3-diyl)-D-allo-heptononitrile 
• 222854-81-1 N-tert-butoxycarbonyl-2,3,6-trideoxy-3,6-imino-5,7-O-(1,1,3,3-tetraisopropyldisiloxa-1,3-diyl)-D-allo-heptononitrile 
• 222854-83-3 N-tert-butoxycarbonyl-2,3,4,6-tetradeoxy-3,6-imino-5,7-O-(1,1,3,3-tetraisopropyldisiloxa-1,3-diyl)-D-ribo-heptononitrile 
• 222631-08-5 2-((3aS,4S,6R,6aR)-6-(((tert-butyldimethylsilyl)oxy)methyl)-2,2-dimethyltetrahydro-3aH-[1,3]dioxolo [4,5-c]pyrrol-4-yl)acetonitrile 
• 222631-23-4 N-tert-butoxycarbonyl-2,3,6-trideoxy-3,6-imino-D-allo-heptononitrile 
• 24424-99-5 di-tert-butyl dicarbonate 
• 222631-20-1 2,3,6-trideoxy-3,6-imino-D-allo-heptononitrile 
• 153172-33-9 (3aR,4R,6aS)-4-(((tert-butyldimethylsilyl)oxy)methyl)-2,2-dimethyl-4,6a-dihydro-3aH-[1,3]dioxolo[4,5-c]pyrrole 
• 153172-31-7 (3aR,4R,6aS)-4-({[(tert-butyl)(dimethyl)silyl]oxy}methyl)tetrahydro-2,2-dimethyl-3aH-[1,3]dioxolo[4,5-c]pyrrole 

Downstream Products

• 222854-88-8 2-[4-(3-benzoyl-2-methyl-isothioureido)-5-ethoxycarbonyl-1H-pyrrol-3-yl]-5,5,7,7-tetraisopropyl-tetrahydro-4,6,8-trioxa-1-aza-5,7-disila-cyclopentacyclooctene-1-carboxylic acid tert-butyl ester 
• 222854-86-6 (1R)-1-[3-amino-1-N-benzyloxycarbonyl-2-ethoxycarbonylpyrrol-4-yl]-N-tert-butoxycarbonyl-1,2,4-trideoxy-1,4-imino-3,5-O-(1,1,3,3-tetraisopropyldisiloxa-1,3-diyl)-D-erythro-pentitol 
• 222854-89-9 2-(2-amino-4-oxo-4,5-dihydro-3H-pyrrolo[3,2-d]pyrimidin-7-yl)-5,5,7,7-tetraisopropyl-tetrahydro-4,6,8-trioxa-1-aza-5,7-disila-cyclopentacyclooctene-1-carboxylic acid tert-butyl ester 
• 222854-87-7 (1R)-N-tert-butoxycarbonyl-1,2,4-trideoxy-1-(9-deazahypoxanthin-9-yl)-1,4-imino-3,5-O-(1,1,3,3-tetraisopropyldisiloxa-1,3-diyl)-D-erythro-pentitol 
• 222854-85-5 (2R,3aS,9aR)-2-[(Z)-1-Cyano-2-(ethoxycarbonylmethyl-amino)-vinyl]-5,5,7,7-tetraisopropyl-tetrahydro-4,6,8-trioxa-1-aza-5,7-disila-cyclopentacyclooctene-1-carboxylic acid tert-butyl ester 

Relevant articles and documents

Synthesis of transition state analogue inhibitors for purine nucleoside phosphorylase and N-riboside hydrolases

Syntheses of the 'Immucillins', potent aza-C-nucleoside inhibitors of purine nucleoside phosphorylase are reported as well as those of 5-deoxy-, 5- deoxyfluoro- and 2-deoxy- analogues and others having modified bases. (C) 2000 Elsevier Science Ltd.