2221-10-5 Usage
General Description
2,4-Imidazolidinedione, 1,5-dimethyl-3-phenyl- is a chemical compound with the molecular formula C11H13N3O2. It is a white, crystalline powder that is commonly used as a reagent in organic synthesis and pharmaceutical manufacturing. This chemical is known for its ability to act as a versatile building block in the production of various pharmaceutical compounds, including antiepileptic drugs and antihypertensive medications. It possesses both antibacterial and antifungal properties, making it a valuable component in the development of antimicrobial agents. The compound also exhibits promising potential in the field of agricultural chemistry, particularly in the formulation of pesticides. Overall, 2,4-Imidazolidinedione, 1,5-dimethyl-3-phenyl- is a valuable chemical with diverse applications in the pharmaceutical, agricultural, and chemical industries.
Check Digit Verification of cas no
The CAS Registry Mumber 2221-10-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,2,2 and 1 respectively; the second part has 2 digits, 1 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 2221-10:
(6*2)+(5*2)+(4*2)+(3*1)+(2*1)+(1*0)=35
35 % 10 = 5
So 2221-10-5 is a valid CAS Registry Number.
2221-10-5Relevant articles and documents
Changes in the relative contribution of specific and general base catalysis in cationic micelles. The cyclization of substituted ethyl hydantoates
Blagoeva,Toteva,Ouarti,Ruasse
, p. 2123 - 2130 (2007/10/03)
The rate-surfactant profiles for the HO-- and AcO--catalyzed ring closure of two ethyl hydantoates, E2 and E3, to hydantoins with three cetyltrimethylammonium salts (CTAX, X = Br-, Cl-, or AcO-) are m
Change of Rate Determining Step Induced by the gem-Dimethyl Effekt
Blagoeva, Iva B.,Tashev, Denis T.,Kirby, Anthony J.
, p. 1157 - 1158 (2007/10/02)
The base-catalysed cyclisation to the hydantoin of 2,2,3-trimethyl-5-phenylhydantoate (2; R1 = R2 = Me) is slower than that of the 2,3-dimethyl compound, even though the acceleration expected from the gem-dimethyl effect is observed for the acid-catalysed
Photochemical decomposition of phenazone derivatives. Part 7: Mechanism of decomposition in aqueous solutions
Marciniec
, p. 180 - 182 (2007/10/02)
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