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378755

Sigma-Aldrich

Dichlorotriphenylphosphorane

95%

Synonym(s):

Triphenylphosphine dichloride

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About This Item

Linear Formula:
(C6H5)3PCl2
CAS Number:
Molecular Weight:
333.19
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22

Quality Level

Assay

95%

form

solid

mp

85 °C (dec.) (lit.)

SMILES string

ClP(Cl)(c1ccccc1)(c2ccccc2)c3ccccc3

InChI

1S/C18H15Cl2P/c19-21(20,16-10-4-1-5-11-16,17-12-6-2-7-13-17)18-14-8-3-9-15-18/h1-15H

InChI key

ASWXNYNXAOQCCD-UHFFFAOYSA-N

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General description

Dichlorotriphenylphosphorane (Triphenylphosphine dichloride, PPh3Cl2) is a phosphorous halide. Stability and reactivity of dichlorotriphenylphosphorane have been studied by solid state 31P NMR spectroscopy. It participates in the conversion of carboxylic esters to acid halides and mechanism of this cleavage has been investigated. Modified method has been proposed in which dichlorotriphenylphosphorane participates in the synthesis of tertiary amides.

Application

Dichlorotriphenylphosphorane may be used in the synthesis of the following:
  • tertiary benzanilide derivatives
  • N-phosphodipeptides
  • dialkyl phosphorochloridites based on the reaction of trialkyl phosphites
  • naphthalene ring-based calix[3]amide, via reaction with 6-amino-2-naphthoic acid
  • C2v-symmetrical cyclic tetramers of aromatic amides

Signal Word

Danger

Hazard Statements

Hazard Classifications

Carc. 1B - Eye Dam. 1 - Flam. Sol. 2 - Skin Corr. 1B

Storage Class Code

4.1B - Flammable solid hazardous materials

WGK

WGK 3

Flash Point(F)

68.0 °F - closed cup

Flash Point(C)

20 °C - closed cup


Regulatory Listings

Regulatory Listings are mainly provided for chemical products. Only limited information can be provided here for non-chemical products. No entry means none of the components are listed. It is the user’s obligation to ensure the safe and legal use of the product.

EU REACH SVHC Candidate List

CAS No.

EU REACH Annex XVII (Restriction List)

CAS No.

EU REACH Annex XIV (Authorisation List)

CAS No.

Certificates of Analysis (COA)

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The preparation of dimethyl phosphorochloridite and its homologs from trialkyl phosphites and dichlorotriphenylphosphorane.
Majewski P.
Phosph. Sulfur Relat. Elem., 33(1-2), 37-39 (1987)
Synthesis, crystal structure and dynamic behavior of naphthalene-based calix [3] amide: Cyclic trimers of 2-alkylamino-6-naphthoic acid.
Katagiri K, et al.
Journal of Molecular Structure, 891(1), 346-350 (2008)
Synthesis of N-Phosphopeptides Coupled by Dichlorotriphenylphosphorane.
Dong S-Z, et al.
Synthetic Communications, 31(13), 2067-2075 (2001)
Simple and convenient synthesis of tertiary benzanilides using dichlorotriphenylphosphorane.
Azumaya I, et al.
Tetrahedron, 59(13), 2325-2331 (2003)
Murali K Urlam et al.
MedChemComm, 4(6), 932-941 (2013-09-28)
The

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