1208538-52-6 Usage
General Description
4-Bromo-2-(methylsulfonyl)pyrimidine is a chemical compound with the molecular formula C6H6BrN3O2S. It is a white to light brown crystalline solid that is primarily used in the synthesis of pharmaceuticals, agrochemicals, and other organic compounds. This chemical is a versatile building block for the synthesis of heterocyclic compounds and is often utilized as a reagent in organic synthesis. It has potential applications in the development of new drugs and is also used as an intermediate in the production of various compounds. Additionally, it is important to handle this chemical with care as it can be harmful if ingested, inhaled, or comes into contact with the skin or eyes.
Check Digit Verification of cas no
The CAS Registry Mumber 1208538-52-6 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,0,8,5,3 and 8 respectively; the second part has 2 digits, 5 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 1208538-52:
(9*1)+(8*2)+(7*0)+(6*8)+(5*5)+(4*3)+(3*8)+(2*5)+(1*2)=146
146 % 10 = 6
So 1208538-52-6 is a valid CAS Registry Number.
1208538-52-6Relevant articles and documents
INHIBITORS OF WDR5 PROTEIN-PROTEIN BINDING
-
, (2017/09/15)
The present application is directed to compounds of Formula I: compounds comprising these compounds and their uses, for example as medicaments for the treatment of diseases, disorders or conditions mediated or treatable by inhibition of binding between WDR5 protein and its binding partners.
Synthesis of cytimidine through a one-pot copper-mediated amidation cascade
Serrano, Catherine M.,Looper, Ryan E.
supporting information; experimental part, p. 5000 - 5003 (2011/11/13)
A concise synthesis of cytimidine was developed utilizing tandem Cu-mediated N-aryl amidations followed by global deprotection. This sequence exploits a regioselective coupling of an iodobenzamide with a halopyrimidine that allows the union of three fragments in a single synthetic manipulation and will permit the efficient and rapid diversification of the cytimidine core.
