28969-60-0 Usage
Uses
Used in Pharmaceutical Industry:
4-Amino-2,5,6-trichloropyrimidine is used as an intermediate in the synthesis of pharmaceuticals for its potential to contribute to the development of new drugs. Its strong antifungal and antibacterial properties are particularly beneficial in creating treatments for various infections.
Used in Agrochemical Industry:
In the agrochemical sector, 4-Amino-2,5,6-trichloropyrimidine serves as a key building block in the production of herbicides and fungicides. Its effectiveness against fungi and bacteria aids in protecting crops from diseases and enhancing agricultural productivity.
Used in Dye Industry:
4-Amino-2,5,6-trichloropyrimidine is also utilized in the dye industry, where it acts as an intermediate for synthesizing various dyes. Its chemical properties allow for the creation of a range of colorants used in different applications.
Safety Note:
It is crucial to handle 4-Amino-2,5,6-trichloropyrimidine with care due to its toxic nature. It can cause skin and eye irritation upon contact, necessitating proper safety measures during its use in laboratories and industrial settings.
Check Digit Verification of cas no
The CAS Registry Mumber 28969-60-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,8,9,6 and 9 respectively; the second part has 2 digits, 6 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 28969-60:
(7*2)+(6*8)+(5*9)+(4*6)+(3*9)+(2*6)+(1*0)=170
170 % 10 = 0
So 28969-60-0 is a valid CAS Registry Number.
InChI:InChI=1/C4H2Cl3N3/c5-1-2(6)9-4(7)10-3(1)8/h(H2,8,9,10)
28969-60-0Relevant academic research and scientific papers
4 - AMINOPYRIMIDINE DERIVATIVES AND THEIR AS AS ADENOSINE A2A RECEPTOR ANTAGONISTS
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Page/Page column 24-25, (2011/10/13)
New 4-amino-pyrimidine derivatives as potent antagonists of the adenosine A2a receptor of formula (I). The invention provides as well a method for preparing such compounds, pharmaceutical compositions comprising an effective amount of these com
MECHANISM FOR REACTIONS OF HALOGENATED COMPOUNDS. PART 4. ACTIVATING INFLUENCES OF RING-NITROGEN AND TRIFLUOROMETHYL IN NUCLEOPHILIC AROMATIC SUBSTITUTION
Chambers, R. D.,Martin, P. A.,Waterhouse, J. S.,Williams, D. L. H.,Anderson, B.
, p. 507 - 514 (2007/10/02)
Rate constants have been measured for the reactions of ammonia with various fluorinated pyridines and diazines in aqueous dioxan at 25 deg C.From the results the activating effects of ring-nitrogen (relative to C-H) and of trifluoromethyl (relative to -H)
