6554-65-0 Usage
Uses
Used in Pharmaceutical Industry:
PyriMidine, 2,4-dichloro-6-ethylis used as a chemical intermediate for the synthesis of various pharmaceutical compounds. Its unique structure allows for the development of new drugs with potential therapeutic applications.
Used in Agrochemical Industry:
In the agrochemical sector, PyriMidine, 2,4-dichloro-6-ethylserves as a key intermediate in the production of agrochemicals. Its incorporation into these products can enhance their effectiveness in agricultural applications.
Used in Organic Synthesis:
PyriMidine, 2,4-dichloro-6-ethylis utilized as a building block in organic synthesis, contributing to the creation of a wide range of organic compounds for various industrial applications. Its presence in these compounds can improve their performance and properties.
Check Digit Verification of cas no
The CAS Registry Mumber 6554-65-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,5,5 and 4 respectively; the second part has 2 digits, 6 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 6554-65:
(6*6)+(5*5)+(4*5)+(3*4)+(2*6)+(1*5)=110
110 % 10 = 0
So 6554-65-0 is a valid CAS Registry Number.
InChI:InChI=1/C6H6Cl2N2/c1-2-4-3-5(7)10-6(8)9-4/h3H,2H2,1H3
6554-65-0Relevant academic research and scientific papers
Pyrimidine derivatives and processes for the preparation thereof
-
, (2008/06/13)
The present invention relates to novel pyrimidine derivatives of the formulae (I-1) and (I-2) and pharmaceutically acceptable salts thereof which possess an excellent anti-secretory activity, pharmaceutical compositions containing same as an active ingredient, their novel intermediates, and processes for the preparation thereof: STR1 wherein: R4 and R5, which may be the same or different, are independently hydrogen or a C1 -C3 alkyl group, or jointly form a cyclopentyl or cyclohexyl ring; A is a group of formula(II): STR2 wherein R1 and R2 are, independently of each other, hydrogen or a C1 -C3 alkyl group, and R3 is hydrogen, a C1 -C3 alkyl group or a halogen; and B is 1-(substituted)-1,2,3,4-tetrahydroisoquinolin-2-yl of formula (III-1) or 7-(substituted)-4,5,6,7-tetrahydrothieno?2,3-c!pyridin-6-yl of formula (III-2) STR3 wherein R6 is hydrogen or a C1 -C3 alkyl group.
