Cas no 3743-07-5 (Dimethyl Chlorophosphite)

Dimethyl Chlorophosphite (CAS 15715-41-0) is an organophosphorus compound with the formula (CH?O)?PCl. It serves as a versatile intermediate in organic synthesis, particularly in the preparation of phosphonates and phosphoramidites. The compound is valued for its high reactivity, enabling efficient phosphorylation reactions under mild conditions. Its low molecular weight and liquid state at room temperature facilitate easy handling and precise dosing in laboratory and industrial applications. Dimethyl Chlorophosphite is commonly used in the production of agrochemicals, flame retardants, and pharmaceuticals. Proper storage under inert conditions is recommended due to its sensitivity to moisture and potential reactivity with nucleophiles.
Dimethyl Chlorophosphite structure
Dimethyl Chlorophosphite structure
Product Name:Dimethyl Chlorophosphite
CAS No:3743-07-5
MF:C2H6ClO2P
MW:128.494600772858
CID:313663
PubChem ID:138038
Update Time:2025-06-10

Dimethyl Chlorophosphite Chemical and Physical Properties

Names and Identifiers

    • Phosphorochloridousacid, dimethyl ester
    • DIMETHYLCHLOROPHOSPHITE
    • Chlorodimethoxyphosphine
    • Dimethoxychlorophosphine
    • Dimethyl phosphorochloridite
    • FT-0769447
    • DTXSID00190874
    • 3743-07-5
    • dimethyl chlorophosphite
    • SCHEMBL2220875
    • AKOS006275864
    • phosphorigsaeure-chlorid-dimethylester
    • Dimethyl Chlorophosphite
    • Inchi: 1S/C2H6ClO2P/c1-4-6(3)5-2/h1-2H3
    • InChI Key: NNPCWHQMEPPTJV-UHFFFAOYSA-N
    • SMILES: ClP(OC)OC

Computed Properties

  • Exact Mass: 127.97900
  • Monoisotopic Mass: 127.979
  • Isotope Atom Count: 0
  • Hydrogen Bond Donor Count: 0
  • Hydrogen Bond Acceptor Count: 2
  • Heavy Atom Count: 6
  • Rotatable Bond Count: 2
  • Complexity: 30.7
  • Covalently-Bonded Unit Count: 1
  • Defined Atom Stereocenter Count: 0
  • Undefined Atom Stereocenter Count : 0
  • Defined Bond Stereocenter Count: 0
  • Undefined Bond Stereocenter Count: 0
  • XLogP3: 0.8
  • Topological Polar Surface Area: 18.5?2

Experimental Properties

  • Boiling Point: 96°Cat760mmHg
  • Flash Point: 11.8°C
  • PSA: 32.05000
  • LogP: 1.74490

Dimethyl Chlorophosphite Customs Data

  • HS CODE:2931900090
  • Customs Data:

    China Customs Code:

    2931900090

    Overview:

    2931900090. Other organic-Inorganic compound. VAT:17.0%. Tax refund rate:13.0%. Regulatory conditions:AB(Customs clearance form for Inbound Goods,Customs clearance form for outbound goods). MFN tariff:6.5%. general tariff:30.0%

    Summary:

    2931900090. other organo-inorganic compounds. VAT:17.0%. Tax rebate rate:13.0%. Supervision conditions:AB(certificate of inspection for goods inward,certificate of inspection for goods outward). MFN tariff:6.5%. General tariff:30.0%

Dimethyl Chlorophosphite Pricemore >>

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D471700-2.5g
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Dimethyl Chlorophosphite Production Method

Production Method 1

Reaction Conditions
Reference
Reaction of chlorophosphoranes with trialkyl phosphites
Gazizov, M. B.; et al, Zhurnal Obshchei Khimii, 1986, 56(7), 1659-60

Dimethyl Chlorophosphite Raw materials

Dimethyl Chlorophosphite Preparation Products

Additional information on Dimethyl Chlorophosphite

Dimethyl Chlorophosphite (CAS No. 3743-07-5): An Overview of Its Properties, Applications, and Recent Research

Dimethyl Chlorophosphite (CAS No. 3743-07-5) is a versatile compound with significant applications in various fields, including organic synthesis, pharmaceuticals, and materials science. This phosphorus-containing compound is characterized by its unique chemical structure and reactivity, making it an essential building block in the synthesis of a wide range of functional molecules.

The chemical formula of Dimethyl Chlorophosphite is CH3O-P(O)-Cl-CH3. It is a colorless liquid with a molecular weight of approximately 115.97 g/mol. The compound is highly reactive due to the presence of the phosphorus-chlorine bond, which can readily undergo nucleophilic substitution reactions. This reactivity makes Dimethyl Chlorophosphite an important intermediate in the synthesis of organophosphorus compounds, which are widely used in agrochemicals, pharmaceuticals, and other industrial applications.

In the field of organic synthesis, Dimethyl Chlorophosphite is often used as a phosphorus donor in the preparation of phosphonates and phosphinates. These derivatives are crucial in the development of novel catalysts and ligands for asymmetric synthesis. For example, recent research has shown that Dimethyl Chlorophosphite-derived phosphonates can be used to create highly efficient chiral catalysts for enantioselective reactions. These catalysts have found applications in the synthesis of chiral pharmaceutical intermediates and fine chemicals.

The pharmaceutical industry has also benefited from the use of Dimethyl Chlorophosphite. In drug discovery and development, this compound serves as a key intermediate in the synthesis of various active pharmaceutical ingredients (APIs). For instance, it has been utilized in the preparation of antiviral agents, anti-inflammatory drugs, and anticancer compounds. Recent studies have highlighted its role in the synthesis of novel antiviral agents that show promising activity against emerging viral pathogens.

In materials science, Dimethyl Chlorophosphite is used to synthesize phosphorus-containing polymers and coatings. These materials exhibit unique properties such as flame retardancy, thermal stability, and enhanced mechanical strength. Recent advancements in polymer chemistry have led to the development of new phosphorus-based materials with improved performance characteristics. For example, phosphorus-containing flame retardants derived from Dimethyl Chlorophosphite have been shown to provide superior fire safety without compromising material properties.

The environmental impact of using Dimethyl Chlorophosphite has also been a subject of recent research. Efforts are being made to develop more sustainable and environmentally friendly processes for its production and use. Green chemistry principles are being applied to minimize waste generation and reduce the environmental footprint associated with its industrial applications. This includes the development of catalytic processes that operate under milder conditions and use less hazardous reagents.

Safety considerations are paramount when handling Dimethyl Chlorophosphite. While it is not classified as a hazardous substance under current regulations, proper handling procedures should be followed to ensure worker safety and environmental protection. This includes using appropriate personal protective equipment (PPE) and working in well-ventilated areas to minimize exposure risks.

In conclusion, Dimethyl Chlorophosphite (CAS No. 3743-07-5) is a multifunctional compound with a wide range of applications in organic synthesis, pharmaceuticals, and materials science. Its unique chemical properties make it an indispensable reagent in the development of new materials and pharmaceuticals. Ongoing research continues to uncover new uses and improve existing applications, ensuring that this compound remains a valuable tool in various scientific disciplines.

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