82264-50-4 Usage
Description
[(AMINOCARBONYL)AMINO](PHENYL)ACETIC ACID, also known as C4, is a chemical compound with the formula C9H11NO3. It is a derivative of acetic acid and contains both an amino and a carboxyl group. [(AMINOCARBONYL)AMINO](PHENYL)ACETIC ACID is a white to off-white solid at room temperature and is soluble in organic solvents, making it a versatile component in chemical reactions and processes.
Uses
Used in Pharmaceutical Industry:
[(AMINOCARBONYL)AMINO](PHENYL)ACETIC ACID is used as a building block for the synthesis of various pharmaceuticals. Its presence of both amino and carboxyl groups allows for the creation of a wide range of organic molecules, making it a valuable intermediate in drug development.
Used in Agrochemical Industry:
In the agrochemical industry, [(AMINOCARBONYL)AMINO](PHENYL)ACETIC ACID is used as a starting material for the production of herbicides and insecticides. Its chemical properties and reactivity contribute to the development of effective and targeted agricultural chemicals.
Used in Chemical Reactions and Processes:
Due to its solubility in organic solvents and the presence of functional groups, [(AMINOCARBONYL)AMINO](PHENYL)ACETIC ACID is used as a versatile component in various chemical reactions and processes, facilitating the synthesis of a broad spectrum of organic molecules for different applications.
Check Digit Verification of cas no
The CAS Registry Mumber 82264-50-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,2,2,6 and 4 respectively; the second part has 2 digits, 5 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 82264-50:
(7*8)+(6*2)+(5*2)+(4*6)+(3*4)+(2*5)+(1*0)=124
124 % 10 = 4
So 82264-50-4 is a valid CAS Registry Number.
82264-50-4Relevant articles and documents
Palladium-catalyzed synthesis of substituted hydantoins - A new carbonylation reaction for the synthesis of amino acid derivatives
Beller, Matthias,Eckert, Markus,Moradi, Wahed A.,Neumann, Helfried
, p. 1454 - 1457 (2007/10/03)
One-step synthesis of substituted hydantoins can be achieved by the palladium-catalyzed 'ureidocarbonylation' of aldehydes with urea derivatives and carbon monoxide [Eq. (1)]. This surprisingly selective protocol converts substituted ureas into 1,5- and 1,3,5-substituted hydantoins in yields of up to 93 %.
