56734-11-3 Usage
Uses
Used in Pharmaceutical Industry:
2-METHANESULFONYL-4-PHENYL-PYRIMIDINE is used as a chemical intermediate for the synthesis of various pharmaceuticals, leveraging its unique structure to contribute to the development of new drugs with potential therapeutic properties.
Used in Agrochemical Industry:
In the agrochemical sector, 2-METHANESULFONYL-4-PHENYL-PYRIMIDINE is employed as a precursor in the production of agrochemicals, where its chemical properties are harnessed to create compounds that can be used in agricultural applications.
Used in Organic Synthesis:
2-METHANESULFONYL-4-PHENYL-PYRIMIDINE is utilized as a building block in organic synthesis, enabling the creation of a wide range of novel organic compounds for various applications across different industries.
Check Digit Verification of cas no
The CAS Registry Mumber 56734-11-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,6,7,3 and 4 respectively; the second part has 2 digits, 1 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 56734-11:
(7*5)+(6*6)+(5*7)+(4*3)+(3*4)+(2*1)+(1*1)=133
133 % 10 = 3
So 56734-11-3 is a valid CAS Registry Number.
56734-11-3Relevant academic research and scientific papers
Regiochemistry in Pd-Catalysed Organotin Reactions with Halopyrimidines
Solberg, Jan,Undheim, Kjell
, p. 62 - 68 (2007/10/02)
Chlorines in activated pyrimidine position is replaced by carbon substituents in Pd-catalysed reactions with organotin compounds.The 4(6)-position is more reactive than the 2-position allowing for regioselective coupling in 2,4(6)-dihalopyrimidines.A bromine substituent is required for coupling in the benzenoid 5-position.In 5-bromo-2,4-dichloropyrimidine the 4-chlorine is replaced before the 5-bromine and the latter before the 2-chloro substituent, all in a regioselective manner.The methodology can be used to introduce functionalized carbon substituents into any pyrimidine position.
(Substituted-phenyl)-1,2,4-triazolo[4,3-a]-pyrimidines and (substituted-phenyl)-1,2,4-triazolo[1,5-a]pyrimidines
-
, (2008/06/13)
This disclosure describes substituted 1,2,4-triazolo[1,5-a]pyrimidines and substituted 1,2,4-triazolo[4,3-a]pyrimidines which possess anxiolytic activity.
