80676-54-6 Usage
General Description
2-(butan-2-yl)-1,4,5,6-tetrahydropyrimidine is a chemical compound with the molecular formula C9H18N2. It is a tetrahydropyrimidine derivative that has a butan-2-yl group attached to the nitrogen atom. 2-(butan-2-yl)-1,4,5,6-tetrahydropyrimidine has potential applications in medicinal chemistry, as it may have pharmacological properties due to its chemical structure. Tetrahydropyrimidines are known for their diverse biological activities, and the substitution of the butan-2-yl group may impart specific properties to 2-(butan-2-yl)-1,4,5,6-tetrahydropyrimidine. Further research is needed to fully understand the potential uses and effects of this compound.
Check Digit Verification of cas no
The CAS Registry Mumber 80676-54-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,0,6,7 and 6 respectively; the second part has 2 digits, 5 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 80676-54:
(7*8)+(6*0)+(5*6)+(4*7)+(3*6)+(2*5)+(1*4)=146
146 % 10 = 6
So 80676-54-6 is a valid CAS Registry Number.
80676-54-6Relevant articles and documents
Allenes. Part 45. 2-Alkyltetrahydropyrimidines, 2-Alkylidenetetrahydro-2H-1,3-oxazines, 2-Alkyl-5,6-dihydro-4H-1,3-oxazines and 2-Alkyl-3-cyano-1,4,5,6-tetrahydropyridines from Allenic nitriles.
Fomum, Z. Tanee,Johnson, Andrew,Landor, Stephen R.,Landor, Phyllis D.,Mbafor, Joseph T.,Nkengfack, Augustine E.
, p. 1537 - 1553 (2007/10/02)
The synthesis of 2-alkyl-3,4,5,6-tetrahydropyrimidines, 2-alkylidene-3,4,5,6-tetrahydro-2H-1,3-oxazines, 2-alkyl-5,6-dihydro-4H-1,3-oxazines and 2-alkyl-3-cyano-1,4,5,6-tetrahydropyridines from allenic nitriles is described.Spectroscopic evidence and mechanistic pathways are discussed.
NOVEL SYNTHESES OF DIHYDROOXAZINES, TETRAHYDROPYRIMIDINES AND TETRAHYDROPYRIDINES FROM ALLENYL NITRILES
Landor, Stephen R.,Landor, Phyllis D.,Fomum, Z. Tanee,Mbafor, J. Tanyi
, p. 1889 - 1892 (2007/10/02)
α-Allenylnitriles give dihydrooxazines and tetrahydropyridines with 3-hydroxypropylamine whereas with 1,3-diaminopropane they afforded tetrahydropyrimidines.
