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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(1H,3H)-Quinazolinedione, 5,6,7,8-tetrahydro-

O=c1[nH]c(=O)[nH]c2c1CCCC2 Request for Quotation
Chemical Name: 2,4(1H,3H)-Quinazolinedione, 5,6,7,8-tetrahydro-
CAS Number: 35042-48-9
Product Number: AG00C8WN(AGN-PC-0JRMP6)
Synonyms:
MDL No:
Molecular Formula: C8H10N2O2
Molecular Weight: 166.1772

Identification/Properties

Properties
MP:
305℃(Solv: ethanol (64-17-5))
BP:
455.8°C at 760 mmHg
Storage:
Keep in dry area;2-8℃;
Form:
Solid
Computed Properties
Molecular Weight:
166.18g/mol
XLogP3:
0.2
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
2
Rotatable Bond Count:
0
Exact Mass:
166.074g/mol
Monoisotopic Mass:
166.074g/mol
Topological Polar Surface Area:
58.2A^2
Heavy Atom Count:
12
Formal Charge:
0
Complexity:
281
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-H315-H319-H335
Precautionary Statements:
P261-P305+P351+P338
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

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Chemical Structure


In chemical synthesis, 5,6,7,8-Tetrahydroquinazoline-2,4(1H,3H)-dione serves as a versatile building block with diverse applications. Due to its unique structure and reactivity, it is commonly employed in the construction of complex organic molecules and heterocyclic compounds. This compound can act as a precursor for the synthesis of biologically active molecules, pharmaceuticals, and agrochemicals. Additionally, its presence in the chemical toolbox enables the creation of novel materials and the exploration of new reaction pathways. The utilization of 5,6,7,8-Tetrahydroquinazoline-2,4(1H,3H)-dione in chemical synthesis showcases its significance in advancing the field of organic chemistry and facilitating the development of innovative compounds.