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(R)-(+)-O-Ethyl hydrogen phenylphosphonothioate dicyclohexylammonium salt is a complex organic compound with the chemical formula C20H30NO2PS. It is a chiral molecule, meaning it has a non-superimposable mirror image, and it belongs to the class of phosphonothioates. (R)-(+)-O-Ethyl hydrogen phenylphosphonothioate dicyclohexylammonium salt is characterized by the presence of a phosphorus atom bonded to a sulfur atom, an oxygen atom, and an ethyl group. The dicyclohexylammonium salt part of the molecule consists of two cyclohexyl groups attached to an ammonium ion, which contributes to its overall structure and properties. It is used in various applications, including as a reagent in organic synthesis and as a precursor in the production of certain pharmaceuticals. Due to its specific stereochemistry and unique structure, it plays a role in asymmetric synthesis and has potential applications in the development of enantiomerically pure compounds.

6230-64-4

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6230-64-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 6230-64-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,2,3 and 0 respectively; the second part has 2 digits, 6 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 6230-64:
(6*6)+(5*2)+(4*3)+(3*0)+(2*6)+(1*4)=74
74 % 10 = 4
So 6230-64-4 is a valid CAS Registry Number.

6230-64-4Relevant academic research and scientific papers

Phosphonothioate hydrolysis by molybdocene dichlorides: Importance of metal interaction with the sulfur of the thiolate leaving group

Kuo, Louis Y.,Baker, Devon C.,Dortignacq, Adria K.,Dill, Kristina M.

, p. 4759 - 4765 (2013/09/24)

The metallocene bis(cyclopentadienyl)molybdenum(IV) dichloride Cp 2MoCl2 hydrolyzes O,S-diethyl phenylphosphonothioate (1) with only P-S scission to yield a phosphonate under mild aqueous conditions. In terms of degrading phosphonoth

Stereochemical inversion of phosphonothioate methanolysis by La(III) and Zn(II): Mechanistic implications for the degradation of organophosphate neurotoxins

Kuo, Louis Y.,Glazier, Sara K.

experimental part, p. 328 - 335 (2012/03/12)

The utility of phosphonothioate methanolysis to degrade organophosphate neurotoxins has prompted the stereochemical investigation of this useful transformation. The methanolysis of enantiomerically pure O,S-diethyl phenylphosphonothioate (5) was studied b

Kinetic Facial Selectivity in Nucleophilic Displacements at Tetracoordinate Phosphorus: Kinetics and Stereochemistry in the Reaction of Sodium Ethoxide with O,S-Dimethyl Phenylphosphonothioate

DeBruin, Kenneth E.,Tang, Chen-lan W.,Johnson, David M.,Wilde, Ronnie L.

, p. 5871 - 5879 (2007/10/02)

The reaction of ethoxide ion with O,S-dimethyl phenylphosphonothioate (1a) proceeds with competitive displacements of the methylthio and methoxy ligands.Each displacement occurs with complete inversion of configuration.The two products, ethyl methyl pheny

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