81741-70-0

Usage

Uses

Used in Organic Synthesis:
[1,3,2]Oxazaphospholo[2,3-b][1,3,2]oxazaphosphole-2,6(3H,5H)-dione, 8,8-dihydro-8-phenylis used as a key intermediate in the synthesis of various complex organic molecules. Its unique structure allows for the creation of a wide range of compounds with potential applications in different industries.
Used in Medicinal Chemistry:
In the field of medicinal chemistry, [1,3,2]Oxazaphospholo[2,3-b][1,3,2]oxazaphosphole-2,6(3H,5H)-dione, 8,8-dihydro-8-phenylis utilized as a building block for the development of novel pharmaceuticals. Its incorporation into drug candidates can lead to the discovery of new treatments for various diseases and conditions.
Used in Pharmaceutical Research:
[1,3,2]Oxazaphospholo[2,3-b][1,3,2]oxazaphosphole-2,6(3H,5H)-dione,
8,8-dihydro-8-phenylis also used in pharmaceutical research to study its potential interactions with biological targets, such as enzymes and receptors. Understanding these interactions can provide valuable insights into the design of new drugs with improved efficacy and selectivity.
Used in Chemical Reactivity Studies:
Due to its unique structure, [1,3,2]Oxazaphospholo[2,3-b][1,3,2]oxazaphosphole-2,6(3H,5H)-dione, 8,8-dihydro-8-phenylis employed in chemical reactivity studies to explore its potential as a catalyst or reactant in various chemical reactions. This can lead to the development of new synthetic methods and the creation of novel compounds with specific properties.

Upstream product

• 644-97-3 Dichlorophenylphosphine 
• 142-73-4 iminodiacetic acid 

Downstream Products

• 145680-31-5 6a-(2-Methyl-3-oxo-1,4,6,9-tetraoxa-5λ⁵-phospha-spiro[4.4]non-2-yl)-6a-phenyl-1,6-dioxa-3a-aza-6aλ⁵-phospha-pentalene-2,5-dione 
• 145587-40-2 C₂₆H₂₅N₂O₁₄P₃ 
• 145587-35-5 2-(2,5-Dioxo-6a-phenyl-tetrahydro-1,6-dioxa-3a-aza-6aλ⁵-phospha-pentalen-6a-yl)-2-hydroxy-propionic acid; compound with triethyl-amine 
• 81733-48-4 6a-Phenyl-6a-phenylamino-1,6-dioxa-3a-aza-6aλ⁵-phospha-pentalene-2,5-dione 
• 143490-00-0 6a-Butoxy-6a-phenyl-1,6-dioxa-3a-aza-6aλ⁵-phospha-pentalene-2,5-dione 
• 143490-02-2 6a-Isopropoxy-6a-phenyl-1,6-dioxa-3a-aza-6aλ⁵-phospha-pentalene-2,5-dione 
• 145587-37-7 2-(2,5-Dioxo-6a-phenyl-tetrahydro-1,6-dioxa-3a-aza-6aλ⁵-phospha-pentalen-6a-yl)-2-hydroxy-pentanedioic acid; compound with triethyl-amine 
• 145587-37-7 2-(2,5-Dioxo-6a-phenyl-tetrahydro-1,6-dioxa-3a-aza-6aλ⁵-phospha-pentalen-6a-yl)-2-hydroxy-pentanedioic acid; compound with triethyl-amine 
• 81733-47-3 2,5-Dioxo-6a-phenyl-tetrahydro-1,6-dioxa-3a-aza-6aλ⁵-phospha-pentalene-6a-carbodithioic acid; compound with triethyl-amine 
• 81733-45-1 6a-Benzyl-6a-phenyl-1,6-dioxa-3a-aza-6aλ⁵-phospha-pentalene-2,5-dione 
• 1754-49-0 diethyl phenylphosphonate 
• 172487-18-2 ethyl Phenylphosphinate 
• 129868-33-3 6a-Phenyl-6a-(1,3,5,7-tetramethyl-2,6-dioxo-1,3,5,7-tetraaza-4λ⁵-phospha-spiro[3.3]hept-4-yl)-1,6-dioxa-3a-aza-6aλ⁵-phospha-pentalene-2,5-dione 
• 143489-98-9 6a-Ethoxy-6a-phenyl-1,6-dioxa-3a-aza-6aλ⁵-phospha-pentalene-2,5-dione 

Relevant academic research and scientific papers

ALKOXYLATION OF HYDRIDOPHOSPHORANES

The bicyclic hydridophosphorane 3 reacted with a series of alcohols in the presence of phenyl disulfide to give the corresponding isolable alkoxyphosphoranes.The reactivities of the alcohols in this reaction were seen to be dependent on the steric hindrance of the R groups.The mechanism was suggested in terms of experimental observation.Key words: Alkoxylation; hydridophosphoranes; scission reaction; phenyl disulfide; alkoxyphosphoranes; steric size.

Acidite de Broensted des phosphoranes a liaison P-H; identification de leurs bases conjuguees; determination de leur pKa

The P-H proton of phosphoranes containing an α-hydroxy acid or iminodiacetic acid ligand is sufficiently mobile to be removed at room temperature by medium strength bases such as triethylamine.The deprotonation products identified by 31P nmr are (a) the p