138548-34-2 Usage
Uses
Used in Pharmaceutical Synthesis:
2,4,6(1H,3H,5H)-Pyrimidinetrione, 5-methyl-1-[(1-oxopropoxy)methyl]-5-phenyl-, (R)is used as an intermediate in the synthesis of pharmaceutical drugs. Its unique structure allows for the development of new drugs with improved efficacy and selectivity.
Used in Agrochemical Synthesis:
In the agrochemical industry, 2,4,6(1H,3H,5H)-Pyrimidinetrione, 5-methyl-1-[(1-oxopropoxy)methyl]-5-phenyl-, (R)is used as a building block for the synthesis of agrochemicals. Its chiral nature and unique functional groups enable the creation of novel agrochemicals with enhanced performance and selectivity.
Used in Specialty Chemicals Production:
2,4,6(1H,3H,5H)-Pyrimidinetrione, 5-methyl-1-[(1-oxopropoxy)methyl]-5-phenyl-, (R)is also used as a starting material for the preparation of specialty chemicals. Its versatile structure allows for the synthesis of a wide range of complex organic molecules, which can be utilized in various industries, such as fragrances, dyes, and coatings.
Check Digit Verification of cas no
The CAS Registry Mumber 138548-34-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,8,5,4 and 8 respectively; the second part has 2 digits, 3 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 138548-34:
(8*1)+(7*3)+(6*8)+(5*5)+(4*4)+(3*8)+(2*3)+(1*4)=152
152 % 10 = 2
So 138548-34-2 is a valid CAS Registry Number.
138548-34-2Relevant academic research and scientific papers
Lipase-catalyzed enantioselective synthesis of optically active mephrobarbital, hexobarbital and febarbamate
Murata,Uchida,Achiwa
, p. 2605 - 2609 (2007/10/02)
Chiral 5,5-disubstituted N-acyloxymethylbarbiturates have been obtained in 40-99% optical yields by lipase-catalyzed hydrolyses of 5,5-disubstituted N,N'-bisacyloxymethylbarbiturates in H2O-saturated diisopropyl ether. These chiral barbiturates
Lipase-catalyzed Enantioselective Hydrolysis of N-Acyloxymethyl Groups in Organic Solvent: Syntheses of Chiral 5,5-Disubstituted 1-Methylbarbiturates
Murata, Masakazu,Achiwa, Kazuo
, p. 6763 - 6766 (2007/10/02)
Chiral 5,5-disubstituted N-acyloxymethylbarbiturates have been obtained in 40-99percent optical yields by lipase-catalyzed hydrolyses of 5,5-disubstituted bisacyloxymethylbarbiturates in H2O-saturated diisopropyl ether.These chiral barbiturates were readi
