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665444

Sigma-Aldrich

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:
41862-14-0
Molecular Weight:
211.26
MDL number:
MFCD01075028
UNSPSC Code:
12352100
PubChem Substance ID:
24884736
NACRES:
NA.22
Pricing and availability is not currently available.

Quality Level

100

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

Related Categories

Application

6-Amino-1,3-dipropyluracil can be used in the synthesis of compounds of medicinal interest such as deazaflavins[1], pyrido[2,3-d]pyrimidines[2][3] and tetrahydrobenzo[g]pyrimido[4,5-c]isoquinoline tetraones.[4]

pictograms

Exclamation mark
GHS07

signalword

Warning

hcodes

H302

Hazard Classifications

Acute Tox. 4 Oral

Storage Class

11 - Combustible Solids

wgk_germany

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

dust mask type N95 (US), Eyeshields, Gloves

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    Certificates of Analysis (COA)

    Lot/Batch Number
    MKCL0667
    MKCD7798
    MKBZ9526V
    MKBZ5690V
    MKBW9743V

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    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)
    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)
    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)
    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)

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