222854-83-3

Basic information

• Product Name: 1,3,5,2,4-Trioxadisilocino7,6-bpyrrole-7(6H)-carboxylic acid, 8-(cyanomethyl)tetrahydro-2,2,4,4-tetrakis(1-methylethyl)-, 1,1-dimethylethyl ester, (6aR,8S,9aS)-
• Synonyms: 1,3,5,2,4-Trioxadisilocino7,6-bpyrrole-7(6H)-carboxylic acid, 8-(cyanomethyl)tetrahydro-2,2,4,4-tetrakis(1-methylethyl)-, 1,1-dimethylethyl ester, (6aR,8S,9aS)-
• CAS NO: 222854-83-3
• Molecular Formula: C24H46 N2 O5 Si2
• Molecular Weight: 498.8
• Mol File: 222854-83-3.mol
• Article Data: 1

Chemical Properties

• Appearance: /
• CAS DataBase Reference: 1,3,5,2,4-Trioxadisilocino7,6-bpyrrole-7(6H)-carboxylic acid, 8-(cyanomethyl)tetrahydro-2,2,4,4-tetrakis(1-methylethyl)-, 1,1-dimethylethyl ester, (6aR,8S,9aS)-(CAS DataBase Reference)
• NIST Chemistry Reference: 1,3,5,2,4-Trioxadisilocino7,6-bpyrrole-7(6H)-carboxylic acid, 8-(cyanomethyl)tetrahydro-2,2,4,4-tetrakis(1-methylethyl)-, 1,1-dimethylethyl ester, (6aR,8S,9aS)-(222854-83-3)
• EPA Substance Registry System: 1,3,5,2,4-Trioxadisilocino7,6-bpyrrole-7(6H)-carboxylic acid, 8-(cyanomethyl)tetrahydro-2,2,4,4-tetrakis(1-methylethyl)-, 1,1-dimethylethyl ester, (6aR,8S,9aS)-(222854-83-3)

Safety Data

• Hazardous Substances Data: 222854-83-3(Hazardous Substances Data)

Usage

Chemical class

Ester derivative

Explanation

The compound is an ester, which is a type of organic compound derived from an acid and an alcohol.

Explanation

The stereochemistry of the compound is specified by the (6aR,8S,9aS) notation, which indicates the spatial arrangement of the atoms in the molecule.

Explanation

These substituents are attached to the main structure of the compound, modifying its properties and reactivity.

Explanation

The compound has chiral centers, which means it can exist in different enantiomeric forms.

Explanation

This formula represents the total number of atoms of each element present in the compound.

Explanation

The molecular weight is the sum of the atomic weights of all the atoms in the molecule.

Explanation

The solubility of the compound is not provided in the material, but it can be inferred that it may be soluble in organic solvents due to its ester and hydrocarbon nature.

Explanation

The reactivity of the compound is not provided in the material, but it can be expected to undergo reactions typical of esters, such as hydrolysis and transesterification.

Explanation

The specific applications of this compound are not provided in the material, but it may have potential uses in various fields, such as pharmaceuticals, materials science, or chemical research.

Functional groups

Trioxadisilocino7,6-bpyrrole-7(6H)-carboxylic acid, cyanomethyl, tetrakis(1-methylethyl), and 1,1-dimethylethyl ester

Stereochemistry

(6aR,8S,9aS)

Substituents

Tetrakis(1-methylethyl) and cyanomethyl

Chirality

Present

Molecular weight

Approximately 529.77 g/mol

Solubility

Unknown

Reactivity

Unknown

Applications

Unknown

Upstream product

• 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 
• 222631-20-1 2,3,6-trideoxy-3,6-imino-D-allo-heptononitrile 
• 24424-99-5 di-tert-butyl dicarbonate 
• 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 
• 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 
• 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 
• 284490-18-2 (2R,3aS,9aR)-2-((Z)-1-Cyano-2-hydroxy-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.