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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)-

2,4-Dichloro-7,7-dimethyl-5,7-dihydrofuro[3,4-d]pyrimidine

Clc1nc(Cl)c2c(n1)C(C)(C)OC2 Request for Quotation
Chemical Name: 2,4-Dichloro-7,7-dimethyl-5,7-dihydrofuro[3,4-d]pyrimidine
CAS Number: 1260088-72-9
Product Number: AG000QRF(AGN-PC-0WAL0H)
Synonyms:
MDL No:
Molecular Formula: C8H8Cl2N2O
Molecular Weight: 219.0679

Identification/Properties

Computed Properties
Molecular Weight:
219.065g/mol
XLogP3:
2
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
0
Exact Mass:
218.001g/mol
Monoisotopic Mass:
218.001g/mol
Topological Polar Surface Area:
35A^2
Heavy Atom Count:
13
Formal Charge:
0
Complexity:
212
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#:
N/A
Hazard Statements:
H302-H315-H319-H332-H335
Precautionary Statements:
P261-P280-P305+P351+P338
Class:
N/A
Packing Group:
N/A

NMR Spectrum

Other Analytical Data

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Chemical Structure


With its unique chemical structure, 2,4-Dichloro-7,7-dimethyl-5,7-dihydrofuro[3,4-d]pyrimidine serves as a versatile and valuable building block in chemical synthesis. This compound plays a crucial role in the development of pharmaceuticals, agrochemicals, and materials science. In chemical synthesis, this compound is used as a key intermediate in the production of various biologically active compounds. Its aromatic ring system and multiple functional groups provide opportunities for diversification through functional group manipulations, such as substitution reactions, oxidations, and reductions. These transformations enable the creation of structurally complex molecules with potential therapeutic or industrial significance.Furthermore, the furo[3,4-d]pyrimidine scaffold present in this compound imparts unique properties to the molecules synthesized, making them attractive candidates for further optimization through structure-activity relationship studies. Overall, the application of 2,4-Dichloro-7,7-dimethyl-5,7-dihydrofuro[3,4-d]pyrimidine in chemical synthesis underscores its importance as a valuable synthon in the development of new chemical entities with diverse applications.