848841-62-3 Usage
General Description
2-BROMO-6-MORPHOLINOPYRAZINE is a chemical compound with the molecular formula C7H9BrN4O, and a molecular weight of 227.077 g/mol. It is a pyrazine derivative that contains a bromine atom and a morpholine ring. 2-BROMO-6-MORPHOLINOPYRAZINE has applications in the pharmaceutical industry as a building block for the synthesis of various organic compounds. It is also used as an intermediate in the production of agrochemicals, dyes, and other specialty chemicals. 2-BROMO-6-MORPHOLINOPYRAZINE is a white to off-white crystalline solid that is soluble in organic solvents, and its properties make it suitable for use in a variety of chemical reactions and processes.
Check Digit Verification of cas no
The CAS Registry Mumber 848841-62-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,4,8,8,4 and 1 respectively; the second part has 2 digits, 6 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 848841-62:
(8*8)+(7*4)+(6*8)+(5*8)+(4*4)+(3*1)+(2*6)+(1*2)=213
213 % 10 = 3
So 848841-62-3 is a valid CAS Registry Number.
InChI:InChI=1/C8H10BrN3O/c9-7-5-10-6-8(11-7)12-1-3-13-4-2-12/h5-6H,1-4H2
848841-62-3Relevant articles and documents
Synthesis of Novel Pyrazine-Substituted 1 H -Pyrrole-2-carboxamides and Related Tethered Heterocycles
Borrows, Rachel,Fairley, Gary,Feron, Lyman J. L.,Grant, Emma,Greenwood, Ryan D. R.,Howells, Rachel L.,Hughes, Samantha,Lamont, Scott G.,Lenz, Eva,McGuire, Thomas M.,Simpson, Iain
, (2022/02/10)
As part of a drug discovery program, 4-pyrazin-2-yl-1H-pyrrole-2-carboxamides were accessed along with a number of bicyclic analogues. Routes to these compounds were largely absent from the scientific literature. The synthesis of a 4-(pyrazin-2-yl)-1H-pyrrole-2-carboxamide and several fused bicyclic analogues all using standard procedures (SNAr, borylation, C C cross couplings, hydrolysis, amide bond formation, cyclisation, halogenation, and alkylation) from readily available starting materials is reported. The synthetic sequences range from 4-2 steps per final compound, with yields of isolated intermediates ranging from 20 to ?100%.
