1006-83-3

Basic information

• Product Name: 1,3,2-Dioxaphospholane, 2-phenyl-
• CAS NO: 1006-83-3
• Molecular Formula: C8H9O2P
• Molecular Weight: 168.132
• Mol File: 1006-83-3.mol
• Article Data: 5

Chemical Properties

• CAS DataBase Reference: 1,3,2-Dioxaphospholane, 2-phenyl-(CAS DataBase Reference)
• NIST Chemistry Reference: 1,3,2-Dioxaphospholane, 2-phenyl-(1006-83-3)
• EPA Substance Registry System: 1,3,2-Dioxaphospholane, 2-phenyl-(1006-83-3)

Safety Data

• Hazardous Substances Data: 1006-83-3(Hazardous Substances Data)

Usage

Structure

Cyclic dioxaphospholane with a phenyl group attached to the second carbon atom in the ring

Functionality

Used as a reagent in organic synthesis

Application

Formation of phosphorus-containing compounds

Potential uses

Studied for its potential application in medicine and materials science

Unique properties

Due to its unique structure and properties

Building block

Can serve as a building block for the synthesis of more complex organic molecules

Upstream product

• 71-43-2 benzene 
• 5865-67-8 dimethyl-2,2 germa-2 dioxolane-1,3 
• 644-97-3 Dichlorophenylphosphine 
• 86853-79-4 2-phenylspiro<1,3,2-dioxaphospholane-2,2'-naphtho<1,8-d,e><1,3,2>dithiaphosphorin> 
• 107-21-1 ethylene glycol 
• 6143-71-1 bis(dimethylamino)phenyl phosphine 

Downstream Products

• 34736-73-7 5-phenyl-1,4,6,9-tetraoxa-5-phosphaspiro<4.4>nonane 
• 17986-57-1 β-chloroethyl phenylphosphinate 
• 13547-39-2 di(β-chloroethyl) phenylphosphonate 
• 13468-89-8 2-phenyl-[1,3,2]dioxaphospholane-2-oxide 
• 638-21-1 phenylphosphane 
• 1779-48-2 phenylphosphinic acid 
• 62620-01-3 Methyl-2,4-diphenyl-1,3,2-dioxaphosphorinan-4-carboxylat-2-oxid 
• 62620-00-2 2-methoxy-3,5-diphenyl-1,4,6,9-tetraoxa-5λ⁵-phospha-spiro[4.4]non-2-ene 
• 33326-01-1 1-(2-hydroxy-ethoxy)-3-methyl-1-phenyl-2,5-dihydro-1H-1λ⁵-phosphol-1-ol 
• 37521-34-9 2,2-Dimethyl-propionic acid 1-[(2-iodo-ethoxy)-phenyl-phosphinoyl]-2-methyl-propenyl ester 
• 37521-33-8 Isobutyric acid 1-[(2-hydroxy-ethoxy)-phenyl-phosphinoyl]-2-methyl-propenyl ester 
• 74-85-1 ethene 
• 57156-84-0 2,4,6-triphenyl-1,3,5-trioxa-3,4,6-triphosphinane-2,4,6-trioxide 
• 75631-05-9 2-oxo-5-phenyl-1,4,6,9-tetraoxa-5-phosphaspiro<4.4>nonane 

Relevant articles and documents

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Preparation method for catalytically compounding benzyl phosphonate by using basic ionic liquid

The invention belongs to the technical field of organic synthesis and relates to a preparation method for benzyl phosphonate as a key intermediate of an acyl phosphine oxide type photoinitiator. According to the method, benzene, phosphorus trichloride and alkyl alcohol are taken as main raw materials and are compounded into benzyl phosphonate through two-step reaction. The preparation method is characterized in that a target product is generated through the low-temperature reaction of the dichlorophenyl phosphine and alcohol under the condition of a gemini basic ionic liquid catalyst in the second step reaction, the reaction temperature is controlled within -10 DEG C to 10 DEG C, the dichlorophenyl phosphine is dropwise added and then the mixture reacts for 0.5-7 hours under a stirring condition after the temperature is increased to 30-50 DEG C. The preparation method has the advantages of low cost, simple and convenient after-treatment, high yield, and the like, and is suitable for industrial production.

Reversible Reaction between Cyclic Phosphonite and Aromatic Cyclic Disulfide To Form a Spiro Dithiolophosphorane. Observation of Reductive Elimination of a Phosphorus(V) Compound

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