6782-00-9 Usage
Uses
Used in Agricultural Chemicals:
Phosphinic acid, (2,6-dimethylphenyl)-, ethyl ester is used as a precursor in the production of pesticides and herbicides. Its unique structure and reactivity contribute to the development of effective agricultural chemicals that protect crops from pests and enhance crop yields.
Used in Pharmaceutical Synthesis:
This ethyl ester derivative of phosphinic acid is also employed in the synthesis of pharmaceuticals. Its specific properties make it a valuable intermediate in the development of new drugs, potentially leading to advancements in medicine and healthcare.
Used in Organic Chemistry Research:
Phosphinic acid, (2,6-dimethylphenyl)-, ethyl ester is utilized in the field of organic chemistry for research purposes. Its unique structure and reactivity provide opportunities for exploring new chemical reactions and mechanisms, contributing to the advancement of organic chemistry knowledge.
Used in Industrial Applications:
This chemical compound has a wide range of industrial applications beyond agriculture and pharmaceuticals. Its versatility in synthesis and reactivity makes it a valuable component in the development of various organic compounds and materials, further expanding its utility in diverse industries.
Check Digit Verification of cas no
The CAS Registry Mumber 6782-00-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,7,8 and 2 respectively; the second part has 2 digits, 0 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 6782-00:
(6*6)+(5*7)+(4*8)+(3*2)+(2*0)+(1*0)=109
109 % 10 = 9
So 6782-00-9 is a valid CAS Registry Number.
6782-00-9Relevant academic research and scientific papers
REACTIVITY OF PHOSPHAALKENES
Knaap, Theodorus A. van der,Bickelhaupt, Friedrich
, p. 47 - 50 (2007/10/02)
The reaction of triarylphosphaalkenes with oxidants (O2, S8, Se, Te, H2O2), with orthoquinones, and with Pt(O)- and Ni(O)-complexes is described.
OXIDATION REACTIONS OF PHOSPHAALKENES.
van der Knaap,Klebach,Lournes,Vos,Bickelhaupt
, p. 4026 - 4032 (2007/10/02)
Phosphaalkenes such as left bracket (2,6-dimethylphenyl) (diphenylmethylene)phosphine right bracket are quite reactive in many respects but are rather sluggish in their reaction with oxygen and sulfur. Primary intermediates in the reactions are the oxide, the phosphene and the phosphinidene oxide which together with (thio)benzophenone is formed by oxidative cleavage of the P equals C bond. The occurrence of these unstable intermediates is concluded from their interception by ethanol or water in the oxygen reactions and by ethanol in the sulfur reaction. The mechanism of these reactions and the competition between various reactants are discussed. The structure of the reaction products is determined from their spectral properties and by alternative synthesis along unequivocal routes.
