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2-thioanisyldichlorophosphine is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

253686-37-2

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253686-37-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 253686-37-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,5,3,6,8 and 6 respectively; the second part has 2 digits, 3 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 253686-37:
(8*2)+(7*5)+(6*3)+(5*6)+(4*8)+(3*6)+(2*3)+(1*7)=162
162 % 10 = 2
So 253686-37-2 is a valid CAS Registry Number.

253686-37-2Relevant academic research and scientific papers

2-Thioanisyldichlorophosphine, new starting material for the preparation of multidentate phosphine ligands: Syntheses and characterization of derivatives of 2-anisyl- and 2-thioanisyldichlorophosphines

Laitinen, Riitta H.,Heikkinen, Ville,Haukka, Matti,Koskinen, Ari M.P.,Pursiainen, Jouni

, p. 235 - 242 (2000)

A new aryldichlorophosphine, 2-thioanisyldichlorophosphine, and its anisyl analogue, 2-anisyldichlorophosphine, were prepared by using an organozinc halide reagent of 2-thioanisole or 2-anisole with ethereal solution of PCl3 in refluxing conditions. From these aryldichlorophosphines, eight new multidentate phosphine ligands containing 2-thioanisyl, 4-thioanisyl, 2-anisyl, 1-naphthyl and 9-anthracenyl groups were synthesized and characterized. Characterization was based mainly on NMR spectroscopy and X-ray crystallography. The crystal structures of six ligands are reported. The electronic effects on basicity of ligands are discussed.

Synthesis and applications to asymmetric catalysis of a series of mono- and bis(diazaphospholidine) ligands

Smyth,Tye,Eldred,Alcocka,Wills

, p. 2840 - 2849 (2007/10/03)

The synthesis of a series of closely related mono- and bis(diazaphospholidine) ligands has been achieved using the condensation of a diamine with a bis(dimethylamino)arylphosphine. The resulting ligands have given excellent results in palladium-catalysed allylic substitution reactions to form C-C bonds (up to 89% ee) and C-N bonds (up to 78% ee).

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