58289-29-5 Usage
Uses
Used in Agrochemicals and Pharmaceuticals:
2,6-Dichloro-4-isopropyl-5-nitropyrimidine is used as an intermediate in the synthesis of various agrochemicals and pharmaceuticals. Its unique structure and functional groups make it a valuable component in the development of new and effective compounds for agricultural and medicinal applications.
Used in Organic Synthesis:
2,6-Dichloro-4-isopropyl-5-nitropyrimidine serves as a building block in organic synthesis, allowing chemists to create a wide range of molecules with diverse properties and applications. Its versatility in chemical reactions makes it a valuable tool in the synthesis of complex organic molecules.
Used as a Precursor for Chemical Production:
2,6-Dichloro-4-isopropyl-5-nitropyrimidine is also used as a precursor for the production of other chemicals. Its ability to be modified and transformed into different compounds makes it an essential component in the chemical industry.
Safety Precautions:
It is important to handle 2,6-Dichloro-4-isopropyl-5-nitropyrimidine with care, as it can be harmful if ingested, inhaled, or comes into contact with skin or eyes. Appropriate safety measures should be taken when handling or working with 2,6-Dichloro-4-isopropyl-5-nitropyrimidine to minimize potential risks and ensure the safety of those involved in its production and use.
Check Digit Verification of cas no
The CAS Registry Mumber 58289-29-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,8,2,8 and 9 respectively; the second part has 2 digits, 2 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 58289-29:
(7*5)+(6*8)+(5*2)+(4*8)+(3*9)+(2*2)+(1*9)=165
165 % 10 = 5
So 58289-29-5 is a valid CAS Registry Number.
58289-29-5Relevant academic research and scientific papers
DIHYDROPTERIDINONES I
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Page/Page column 99, (2014/09/03)
The present invention relates to dihydropteridinones, their use as modulators of γ-secretase and to pharmaceutical compositions containing said compounds. In particular, the present invention relates to compounds which interfere with γ-secretase and/or it
DIHYDROPTERIDINONES I
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Paragraph 0548, (2013/09/12)
The present invention relates to dihydropteridinones, their use as modulators of γ-secretase and to pharmaceutical compositions containing said compounds. In particular, the present invention relates to compounds which interfere with γ-secretase and/or it
Structure-Activity Relations. Part 12. Antibacterial Activity of a Series of 2,4-Diamino-6-substituted 5-(4-pyridylmethylamino)pyrimidines and 2,4-Diamino-5-(4-substituted benzylamino)pyrimidines.
Bowden, Keith,Bright, Andrew C.
, p. 514 - 539 (2007/10/02)
A series of 6-substituted 2,4-diamino-5-(4-pyridylamino)pyrimidines and of 2,4-diamino-5-(4-substituted benzylamino)pyrimidines has been prepared.Their antibacterial activity towards L. casei, S. aureus and E. coli has been investigated.These activities have been successfully correlated by Hansch-type relations.Dependence on both lipophilicity and electronic (polar) factors has been found.The results are related to the structure and interactions with the receptor.
