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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-(2-chloroquinazolin-4-yl)acetamide

NC(=O)Cc1nc(Cl)nc2c1cccc2 Request for Quotation
Chemical Name: 2-(2-chloroquinazolin-4-yl)acetamide
CAS Number: 425638-74-0
Product Number: AG00CJE0(AGN-PC-0217YK)
Synonyms:
MDL No:
Molecular Formula: C10H8ClN3O
Molecular Weight: 221.6430

Identification/Properties

Properties
BP:
373°C at 760 mmHg
Storage:
Inert atmosphere;2-8℃;
Computed Properties
Molecular Weight:
221.644g/mol
XLogP3:
1.3
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
2
Exact Mass:
221.036g/mol
Monoisotopic Mass:
221.036g/mol
Topological Polar Surface Area:
68.9A^2
Heavy Atom Count:
15
Formal Charge:
0
Complexity:
249
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


2-(2-Chloroquinazolin-4-yl)acetamide is a versatile compound widely utilized in chemical synthesis for various applications. In organic chemistry, this compound serves as a key building block for the construction of complex molecules due to its functional groups and reactivity. Its chloroquinazoline moiety imparts unique characteristics that make it valuable in the design and creation of novel compounds. This compound is frequently employed in the pharmaceutical industry for the synthesis of potential drug candidates, as well as in academic research for investigating new reaction pathways and molecular transformations. Additionally, 2-(2-Chloroquinazolin-4-yl)acetamide is utilized in material science for producing advanced materials with tailored properties and functions. With its broad utility and significance in chemical synthesis, this compound plays a crucial role in driving innovation and discovery in various scientific fields.