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Safety Information

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:
Molecular Weight:
211.26
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22

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.

Pictograms

Exclamation mark

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

Regulatory Listings

Regulatory Listings are mainly provided for chemical products. Only limited information can be provided here for non-chemical products. No entry means none of the components are listed. It is the user’s obligation to ensure the safe and legal use of the product.

JAN Code

665444-VAR:
665444-5G:
665444-BULK:


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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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