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(γ,γ-Dimethyl-α-carboxy-butyl)-diphenyl-phosphin-sulfid is a complex organic compound characterized by its unique structure. It features a phosphorus atom bonded to a sulfur atom, forming a phosphin-sulfid group. The molecule also includes a diphenyl group, which consists of two phenyl rings attached to the phosphorus. The γ,γ-dimethyl-α-carboxy-butyl moiety adds to the complexity, with two methyl groups at the γ position and a carboxylic acid group at the α position of a butyl chain. (γ,γ-Dimethyl-α-carboxy-butyl)-diphenyl-phosphin-sulfid is known for its potential applications in various chemical and pharmaceutical industries, particularly in the synthesis of certain drugs and as a ligand in coordination chemistry. Its specific properties and reactivity make it a subject of interest for researchers in organic synthesis and material science.

7087-70-9

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7087-70-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 7087-70-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,0,8 and 7 respectively; the second part has 2 digits, 7 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 7087-70:
(6*7)+(5*0)+(4*8)+(3*7)+(2*7)+(1*0)=109
109 % 10 = 9
So 7087-70-9 is a valid CAS Registry Number.

7087-70-9Downstream Products

7087-70-9Relevant academic research and scientific papers

Reactivite carbanionique de l'enchainement PV-CH2-CH2-S-. Application a la synthese d'un nouveau type de coordinats phosphoryles tetradentes

Savignac, Monique,Cadiot, Paul,Mathey, Francois

, p. 840 - 844 (2007/10/02)

The tert-butyllithium metallation of compounds containing the group PV-CH2-CH2-SR proceeds by elimination of the group SR (R = H, CH3) followed by addition of tert-BuLi.Application of this addition-elimination reaction to functionalized phosphine-oxides Φ2P(O)CH2Z (Z = CN, COOEt) leads to the synthesis of γ-diphosphorylated compounds.These dissociate in basic medium following a mechanism which is the reverse of their formation as shown by treatment of the reaction mixture with p-chlorobenzaldehyde to give ethyl p-chlorocinnamate.

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