7040-58-6 Usage
Uses
Used in Organic Synthesis:
3-(3,3-dimethylbutan-2-yloxy-methyl-phosphoryl)oxy-2,2-dimethyl-butane is used as a reagent or intermediate in organic synthesis for its unique phosphorus-containing structure, which can be utilized in the formation of various complex organic molecules.
Used in Materials Science:
In the field of materials science, 3-(3,3-dimethylbutan-2-yloxy-methyl-phosphoryl)oxy-2,2-dimethyl-butane is used as a component in the development of new materials with specific properties, such as flame retardants, polymers, or other specialty materials, due to its phosphorus-based composition and potential reactivity.
Used in Pharmaceutical Industry:
3-(3,3-dimethylbutan-2-yloxy-methyl-phosphoryl)oxy-2,2-dimethyl-butane is used as a precursor or building block in the synthesis of pharmaceutical compounds, leveraging its unique structure to create novel drugs with specific therapeutic properties.
Used in Agrochemical Industry:
In the agrochemical industry, 3-(3,3-dimethylbutan-2-yloxy-methyl-phosphoryl)oxy-2,2-dimethyl-butane is used as a starting material for the synthesis of pesticides or other agrochemicals, taking advantage of its chemical reactivity and potential to form active ingredients with desired biological activity.
Check Digit Verification of cas no
The CAS Registry Mumber 7040-58-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,0,4 and 0 respectively; the second part has 2 digits, 5 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 7040-58:
(6*7)+(5*0)+(4*4)+(3*0)+(2*5)+(1*8)=76
76 % 10 = 6
So 7040-58-6 is a valid CAS Registry Number.
7040-58-6Relevant academic research and scientific papers
Visible-light C-heteroatom bond cleavage and detoxification of chemical warfare agents using titania-supported gold nanoparticles as photocatalyst
Neau, Tefan,Cojocaru, Bogdan,Parvulescu, Vasile I.,Omoghi, Vasile,Alvaro, Mercedes,Garcia, Hermenegildo
supporting information; scheme or table, p. 4050 - 4054 (2011/07/29)
Gold nanoparticles supported on TiO2 effect the detoxification of soman and VX nerve gases and yperite vesicant agent at room temperature upon visible light illumination.
STEREOCHEMISTRY OF SOME REACTIONS BETWEEN ALKYL S-METHYL METHYLPHOSPHONOTHIOATES AND CHIRAL ALKOXIDES
Hall, C. Richard,Inch, Thomas D.,Pottage, Colin,Williams, Nancy E.
, p. 4909 - 4918 (2007/10/02)
With R-(+) ethyl (or methyl) S-methyl methylphosphonothioate and (+)-pinacolyl alkoxide competitive and highly stereoselective displacements of O-alkyl and S-methyl occur, both reactions being with inversion of configuration.With the enantiomeric S-(-) ethyl (and methyl) S-methyl methylphosphonothioates and (+)-pinacolyl alkoxide the reactions, although still competitive, are no longer stereoselective.In contrast similar reactions with the sodium salt of (-)-menthol, (which might be considered to be the mirror image of (+)-pinacolyl alkoxide) occur highly stereoselectively with the S-(-) but not with R-(+) enantiomers.The displacement of O-alkyl from alkyl S-methyl methylphosphonothioates by ethoxide, pinacolyl alkoxide and menthyl alkoxide is not observed when methoxide is the nucleophile; in this case only displacement of S-alkyl group occurs.
