126504-85-6 Usage
Uses
Used in Pharmaceutical Industry:
Pyrimidine, 2-(chloromethyl)-5-methyl serves as a key intermediate in the synthesis of various pharmaceuticals. Its reactivity allows for the development of new drug molecules with potential therapeutic applications, contributing to the advancement of medicinal chemistry.
Used in Agrochemical Industry:
In the agrochemical sector, Pyrimidine, 2-(chloromethyl)-5-methyl is utilized as a starting material for the production of pesticides and other agrochemicals. Its role in the synthesis of these compounds aids in the development of effective solutions for crop protection and management.
Used in Organic Synthesis:
Pyrimidine, 2-(chloromethyl)-5-methyl is employed as a versatile building block in organic synthesis. Its unique structure allows for the creation of a wide range of organic compounds, expanding the scope of chemical research and development.
Used in Chemical Research:
Due to its reactivity and potential applications, Pyrimidine, 2-(chloromethyl)-5-methyl is of interest to researchers in the field of chemistry. It serves as a subject for study, enabling the exploration of new reaction pathways and the discovery of novel chemical properties.
Check Digit Verification of cas no
The CAS Registry Mumber 126504-85-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,6,5,0 and 4 respectively; the second part has 2 digits, 8 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 126504-85:
(8*1)+(7*2)+(6*6)+(5*5)+(4*0)+(3*4)+(2*8)+(1*5)=116
116 % 10 = 6
So 126504-85-6 is a valid CAS Registry Number.
InChI:InChI=1/C6H7ClN2/c1-5-3-8-6(2-7)9-4-5/h3-4H,2H2,1H3
126504-85-6Relevant articles and documents
(2,5)Pyrimidinophanes: Synthesis and Molecular Structure
Eiermann, Uwe,Krieger, Claus,Neugebauer, Franz A.
, p. 1885 - 1889 (2007/10/02)
The title compounds 1 and 2 are synthesized by photolytic sulfur extrusion from 2,11-dithia(2,5)pyrimidinophane 17.The molecular structures of 1 and 2 are determined by X-ray structure analysis and are discussed with regard to the steric strain in these molecules.Thermolysis of - or -trimethylammonium hydroxide (10 or 11) does not generate 1 and 2. α-Chlorination of 2,5-dimethylpyrimidine (3) with N-chlorosuccinimide provides the required precursors 4 - 6.
PHARMACOLOGICALLY ACTIVE GUANIDINE COMPOUNDS
-
, (2008/06/13)
The compounds are substituted thioalkyl-, aminoalkyl-and oxyalkyl-guanidines which are inhibitors of histamine activity.
PHARMACOLOGICALLY ACTIVE THIOUREA AND UREA COMPOUNDS
-
, (2008/06/13)
The compounds are substituted thioalkyl-, aminoalkyl-and oxyalkyl-thioureas and ureas which are inhibitors of histamine activity.
