Dichloro(dimethylamino)phosphine, 98%
Dichloro(dimethylamino)phosphine, 98%
Dichloro(dimethylamino)phosphine, 98%
Thermo Scientific Chemicals

Dichloro(dimethylamino)phosphine, 98%

CAS: 683-85-2 | C2H6Cl2NP | 145.951 g/mol
Quantity:
5 g
25 g
Catalog number H27856.06
also known as H27856-06
Price (JPY)
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Quantity:
5 g
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Chemical Identifiers
CAS683-85-2
IUPAC Name(dichlorophosphanyl)dimethylamine
Molecular FormulaC2H6Cl2NP
InChI KeyXPWWDZRSNFSLRQ-UHFFFAOYSA-N
SMILESCN(C)P(Cl)Cl
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SpecificationsSpecification SheetSpecification Sheet
Appearance (Color)Colorless to pale yellow
FormLiquid
Assay by NMR≥97.5% (Proton NMR)
CommentProduct may contain a small amount of sediment up on standing which does not affect the overall quality of the product.
Proton NMRConforms to structure
Dimethylphosphoramidous dichloride (N,N-dimethylamidodichlorophosphite) may be used in the synthesis of the following N,N-dimethylamidotetrachlorophosphorane, O-propylchloroformimino-N,N-dimethylamidochlorophosphate, bisarylsulphonyldiazadiphosphetidines.

This Thermo Scientific Chemicals brand product was originally part of the Alfa Aesar product portfolio. Some documentation and label information may refer to the legacy brand. The original Alfa Aesar product / item code or SKU reference has not changed as a part of the brand transition to Thermo Scientific Chemicals.

Applications
Dimethylphosphoramidous dichloride (N,N-dimethylamidodichlorophosphite) may be used in the synthesis of the following N,N-dimethylamidotetrachlorophosphorane, O-propylchloroformimino-N,N-dimethylamidochlorophosphate, bisarylsulphonyldiazadiphosphetidines.

Solubility
Reacts with water.

Notes
Moisture Sensitive. Store in cool place. Keep container tightly closed in a dry and well-ventilated place. Store away from strong oxidizing agents, water, moisture, heat.
RUO – Research Use Only

General References:

  1. Sokolov VB, et al. Reaction of 1, 1-dichloro-1-nitrosobutane with N, N-dimethylamidodichlorophosphite. . Bull. Acad. Sci. USSR, Chemistry Series. 1989, 38 (6),1296-1298.
  2. Bowden FL, et al. Organophosphorus chemistry. Part XIV. Reaction of phosphorodiamidous chlorides with sulphonamides: a new route to diazadiphosphetidines.. J. Chem. Soc. Perkin Trans. I1973 , 516-520.