82372-35-8

Usage

Uses

Used in Organic Synthesis:
N,N-Diethyl-1,5-dihydro-2,4,3-benzodioxaphosphepin-3-amine is used as a phosphitylating reagent for organic reactions, enabling the formation of various complex organic compounds.
Used in the Synthesis of Bicyclic Glycosyl Phosphites:
In the field of organic chemistry, N,N-diethyl-1,5-dihydro-2,4,3-benzodioxaphosphepin-3-amine is used as a key intermediate in the synthesis of bicyclic glycosyl phosphitepentakis(o-xylylene phosphate). N,N-DIETHYL-1,5-DIHYDRO-2,4,3-BENZODIOXAPHOSPHEPIN-3-AMINE has potential applications in the development of new pharmaceuticals and materials.
Used in the Synthesis of o-Xylylene Alkyl Phosphites:
N,N-Diethyl-1,5-dihydro-2,4,3-benzodioxaphosphepin-3-amine is also utilized in the synthesis of o-xylylene alkyl phosphites, which are important building blocks in the creation of various organic compounds and materials.

InChI:InChI=1/C12H18NO2P/c1-3-13(4-2)16-14-9-11-7-5-6-8-12(11)10-15-16/h5-8H,3-4,9-10H2,1-2H3

Upstream product

• 612-14-6 phthalyl alcohol 
• 2283-11-6 hexaethylphosphoric triamide 
• 1069-08-5 diethylphosphoramidous dichloride 

Downstream Products

• 173465-81-1 C₁₄₀H₂₁₈N₂O₂₆P₂ 
• 173465-71-9 (R)-3-Tetradecanoyloxy-tetradecanoic acid (2S,3R,4R,5S,6R)-2-allyloxy-6-benzyloxymethyl-3-(9H-fluoren-9-ylmethoxycarbonylamino)-5-(3-oxo-1,5-dihydro-3λ⁵-benzo[e][1,3,2]dioxaphosphepin-3-yloxy)-tetrahydro-pyran-4-yl ester 
• 864951-19-9 (1R,2S,3S,4R)-1-O-benzyl-2,3,4-tris-O-(3-oxo-1,4-dihydro-3λ⁵-2,4,3-benzodioxaphosphepin-3-yl)conduritol B 
• 864951-13-3 (1S,2R,3R,4S)-1-O-benzyl-2,3,4-tris-O-(3-oxo-1,4-dihydro-3λ⁵-2,4,3-benzodioxaphosphepin-3-yl)conduritol B 
• 864373-07-9 1-O-acetyl-3,6-di-O-benzyl-2,4,5-tris-O-(3-oxo-1,5-dihyldro-3λ⁵-2,4,3-benzodioxaphosphepin-3-yl)-D-myo-inositol 
• 864373-02-4 2-O-acetyl-1,4-di-O-benzyl-3,5,6-tris-O-(3-oxo-1,5-dihydro-3λ⁵-2,4,3-benzodioxaphosphepin-3-yl)-D-myo-inositol 
• 864372-86-1 2-O-acetyl-3,6-di-O-benzyl-1,4,5-tris-O-(3-oxo-1,5-dihydro-3λ⁵-2,4,3-benzodioxaphosphepin-3-yl)-D-myo-inositol 
• 864372-77-0 4,5-di-O-acetyl-3,6-di-O-benzyl-1,2-bis-O-(3-oxo-1,5-dihydro-3λ⁵-2,4,3-benzodioxaphosphepin-3-yl)-D-myo-inositol 
• 864372-98-5 5,6-di-O-acetyl-1,4-di-O-benzyl-2,3-bis-O-(3-oxo-1,5-dihydro-3λ⁵-2,4,3-benzodioxaphosphepin-3-yl)-D-myo-inositol 
• 864372-89-4 1,4,5-tri-O-acetyl-3,6-di-O-benzyl-2-O-(3-oxo-1,5-dihydro-3λ⁵-2,4,3-benzodioxaphosphepin-3-yl)-D-myo-inositol 
• 864373-00-2 2,5,6-tri-O-acetyl-1,4-di-O-benzyl-3-O-(3-oxo-1,5-dihydro-3λ⁵-2,4,3-benzodioxaphosphepin-3-yl)-D-myo-inositol 
• 864372-96-3 Acetic acid (1R,2R,3S,4S,5R,6R)-3,4-diacetoxy-2,5-bis-(bis-benzyloxy-phosphoryloxy)-6-(3-oxo-1,5-dihydro-3λ⁵-benzo[e][1,3,2]dioxaphosphepin-3-yloxy)-cyclohexyl ester 

Relevant academic research and scientific papers

Synthesis of a Tethered myo -Inositol (1,3,4,5,6)Pentakisphosphate (IP5) Derivative as a Probe for Biological Studies

There is sufficient evidence to suggest that myo-inositol pentakisphosphate is a vital intermediate species in higher inositol phosphate metabolism, however, its biological roles and physiological function in cells remain uncertain. A tethered myo-inosito

Photo-Arbuzov rearrangements of cyclic phosphite systems

The direct UV irradiation of cyclic phosphites 1-4 was carried out in argon-saturated solvents. In all cases examined, the rearranged, ring-contracted Photo-Arbuzov phosphonate was the major product formed with isolated yields ranging from 40 to 50%. Thes