665444
6-Amino-1,3-dipropyluracil
97%
Synonym(s):
6-Amino-1,3-dipropyl-2,4(1H,3H)-pyrimidinedione
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About This Item
Empirical Formula (Hill Notation):
C10H17N3O2
CAS Number:
Molecular Weight:
211.26
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22
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Assay
97%
form
solid
mp
134-139 °C
SMILES string
CCCN1C(N)=CC(=O)N(CCC)C1=O
InChI
1S/C10H17N3O2/c1-3-5-12-8(11)7-9(14)13(6-4-2)10(12)15/h7H,3-6,11H2,1-2H3
InChI key
WWYIZMBRAYKRFU-UHFFFAOYSA-N
Application
6-Amino-1,3-dipropyluracil can be used in the synthesis of compounds of medicinal interest such as deazaflavins, pyrido[2,3-d]pyrimidines and tetrahydrobenzo[g]pyrimido[4,5-c]isoquinoline tetraones.
Signal Word
Warning
Hazard Statements
Hazard Classifications
Acute Tox. 4 Oral
Storage Class Code
11 - Combustible Solids
WGK
WGK 3
Flash Point(F)
Not applicable
Flash Point(C)
Not applicable
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
Certificates of Analysis (COA)
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Ferrocenyl, Alkyl, and Aryl?Pyrido [2, 3?d] Pyrimidines as Vasorelaxant of Smooth Muscle of Rat Aorta via cAMP Conservation Through Phosphodiesterase Inhibition.
Arellano I, et al.
Journal of Heterocyclic Chemistry, 53(4), 1147-1154 (2016)
Synthesis of Pyrimidine Fused Quinolines by Ligand-Free Copper-Catalyzed Domino Reactions.
Panday A K, et al.
The Journal of Organic Chemistry, 83(7), 3624-3632 (2018)
2, 4-Dialkyl-8, 9, 10, 11-tetrahydrobenzo [g] pyrimido [4, 5-c] isoquinoline-1, 3, 7, 12 (2H, 4H)-tetraones as new leads against Mycobacterium tuberculosis.
Claes P, et al.
European Journal of Medicinal Chemistry, 77, 409-421 (2014)
Cascade imination, Buchwald?Hartwig cross coupling and cycloaddition reaction: synthesis of pyrido [2, 3-d] pyrimidines.
Saikia P, et al.
Royal Society of Chemistry Advances, 5(30), 23210-23212 (2015)
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