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  2. 6-amino-3-(1,1,2,2,3,3,3-heptadeuteriopropyl)-1-propylpyrimidine-2,4-dione

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Brc1cnc(nc1)C
Pyrimidine, 5-bromo-2-methyl-
CCCP1(=O)OP(=O)(CCC)OP(=O)(O1)CCC
1,3,5,2,4,6-Trioxatriphosphorinane, 2,4,6-tripropyl-, 2,4,6-trioxide
CC1(C)OB(OC1(C)C)B1OC(C(O1)(C)C)(C)C
2,2'-Bi-1,3,2-dioxaborolane, 4,4,4',4',5,5,5',5'-octamethyl-
O=C(C=Cc1ccccc1)C=Cc1ccccc1.O=C(C=Cc1ccccc1)C=Cc1ccccc1.O=C(C=Cc1ccccc1)C=Cc1ccccc1.[Pd].[Pd]
Tris(dibenzylideneacetone)dipalladium
C1CCC(CC1)P(C1CCCCC1)C1CCCCC1.Cc1cc(C)c(c(c1)C)N1CCN(C1=[Ru](=Cc1ccccc1)(Cl)Cl)c1c(C)cc(cc1C)C
Ruthenium,[1,3-bis(2,4,6-trimethylphenyl)-2-imidazolidinylidene]dichloro(phenylmethylene)(tricyclohexylphosphine)-, (SP-5-41)-

6-amino-3-(1,1,2,2,3,3,3-heptadeuteriopropyl)-1-propylpyrimidine-2,4-dione

CCCn1c(N)cc(=O)n(c1=O)CCC Request for Quotation
Chemical Name: 6-amino-3-(1,1,2,2,3,3,3-heptadeuteriopropyl)-1-propylpyrimidine-2,4-dione
CAS Number: 41862-14-0
Product Number: AG003N21(AGN-PC-0CTN37)
Synonyms:
MDL No:
Molecular Formula: C10H17N3O2
Molecular Weight: 211.2609

Identification/Properties

Properties
MP:
134-139 °C
BP:
308.3 °C at 760 mmHg
Storage:
Room Temperature;
Form:
Solid
Computed Properties
Molecular Weight:
211.265g/mol
XLogP3:
0.7
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
4
Exact Mass:
211.132g/mol
Monoisotopic Mass:
211.132g/mol
Topological Polar Surface Area:
66.6A^2
Heavy Atom Count:
15
Formal Charge:
0
Complexity:
299
Isotope Atom Count:
0
Defined Atom Stereocenter Count:
0
Undefined Atom Stereocenter Count:
0
Defined Bond Stereocenter Count:
0
Undefined Bond Stereocenter Count:
0
Covalently-Bonded Unit Count:
1
Compound Is Canonicalized:
Yes

Safety Information

GHS Pictogram:
Signal Word:
Warning
UN#:
-
Hazard Statements:
H302
Precautionary Statements:
P280-P305+P351+P338
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

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Chemical Structure


The compound 6-Amino-1,3-dipropylpyrimidine-2,4(1H,3H)-dione, when used in chemical synthesis, serves as a versatile building block for the preparation of various organic compounds. Its unique structure allows it to participate in a range of reactions, leading to the formation of new molecules with diverse functionalities. In particular, this compound can be employed in the synthesis of pharmaceutical intermediates, agrochemicals, and materials science research. The presence of the amino and carbonyl groups in its structure enables it to undergo key chemical transformations, such as acylation, alkylation, and cyclization reactions, facilitating the synthesis of complex molecules with high efficiency. Additionally, the dipropyl substituents on the pyrimidine ring provide steric effects that influence the regioselectivity and stereochemistry of the products formed. Its utilization in chemical synthesis offers a valuable tool for organic chemists to access novel compounds with potential applications in various fields of science and technology.