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665444

Sigma-Aldrich

6-Amino-1,3-dipropyluracil

97%

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Synonym(s):
6-Amino-1,3-dipropyl-2,4(1H,3H)-pyrimidinedione
Empirical Formula (Hill Notation):
C10H17N3O2
CAS Number:
Molecular Weight:
211.26
MDL number:
PubChem Substance ID:

Quality Level

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

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This Item
D15901U0750333778
6-Amino-1,3-dipropyluracil 97%

665444

6-Amino-1,3-dipropyluracil

Uracil ≥99.0%

U0750

Uracil

Uracil-15N2 98 atom % 15N

333778

Uracil-15N2

Quality Level

100

Quality Level

200

Quality Level

300

Quality Level

200

form

solid

form

solid

form

powder

form

solid

mp

134-139 °C

mp

210-214 °C (dec.) (lit.)

mp

>300 °C (lit.)

mp

>300 °C (dec.) (lit.)

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.

pictograms

Exclamation mark

signalword

Warning

hcodes

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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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)
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)

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