6782-00-9 Usage
General Description
Phosphinic acid, (2,6-dimethylphenyl)-, ethyl ester is a chemical compound with the molecular formula C11H17O2P. It is an ethyl ester derivative of phosphinic acid, which is commonly used in the synthesis of organophosphorus compounds. This particular derivative contains a 2,6-dimethylphenyl group, which gives it specific properties and reactivity. It is commonly used as a precursor in the production of pesticides, herbicides, and other agricultural chemicals, as well as in the synthesis of pharmaceuticals and other organic compounds. This chemical is important in the field of organic chemistry and has a wide range of industrial applications.
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 articles and documents
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.