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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)-

1,3-Dioxolo[4,5-g]quinazoline, 8-chloro-

Clc1ncnc2c1cc1OCOc1c2 Request for Quotation
Chemical Name: 1,3-Dioxolo[4,5-g]quinazoline, 8-chloro-
CAS Number: 72700-23-3
Product Number: AG005Q4T(AGN-PC-0031OH)
Synonyms:
MDL No:
Molecular Formula: C9H5ClN2O2
Molecular Weight: 208.6012

Identification/Properties

Properties
BP:
360.3°C at 760 mmHg
Storage:
Keep in dry area;2-8℃;
Computed Properties
Molecular Weight:
208.601g/mol
XLogP3:
2.3
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
4
Rotatable Bond Count:
0
Exact Mass:
208.004g/mol
Monoisotopic Mass:
208.004g/mol
Topological Polar Surface Area:
44.2A^2
Heavy Atom Count:
14
Formal Charge:
0
Complexity:
229
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-H335
Precautionary Statements:
P261-P305+P351+P338
Class:
N/A
Packing Group:
N/A

NMR Spectrum

Other Analytical Data

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Chemical Structure


8-Chloro-[1,3]dioxolo[4,5-g]quinazoline, also known as $name$, is a versatile compound widely utilized in chemical synthesis. This heterocyclic molecule serves as a valuable building block in organic reactions, particularly in the pharmaceutical and agrochemical industries. With its unique structure, 8-Chloro-[1,3]dioxolo[4,5-g]quinazoline can be employed as a key intermediate in the synthesis of various biologically active compounds.One common application of 8-Chloro-[1,3]dioxolo[4,5-g]quinazoline is in the development of novel drug candidates. By incorporating this compound into molecular structures, chemists can modify its properties to enhance the desired biological activity of the final products. Additionally, the reactivity and functional groups present in 8-Chloro-[1,3]dioxolo[4,5-g]quinazoline enable diverse chemical transformations, enabling the synthesis of complex molecules with high efficiency.Moreover, 8-Chloro-[1,3]dioxolo[4,5-g]quinazoline acts as a valuable tool in medicinal chemistry research, aiding in the exploration of new therapeutic agents and drug discovery. Its unique scaffold and versatility make it an integral component in the development of innovative pharmaceutical compounds with potential applications in treating various diseases.In summary, 8-Chloro-[1,3]dioxolo[4,5-g]quinazoline plays a crucial role in chemical synthesis, particularly in the creation of biologically active molecules for pharmaceutical and agrochemical purposes. Its utility and reactivity make it a prized molecule in the hands of synthetic chemists seeking to innovate in the field of drug development and molecular design.