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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)-

Phenol, 3-[(6,7-dimethoxy-4-quinazolinyl)amino]-

COc1cc2c(ncnc2cc1OC)Nc1cccc(c1)O Request for Quotation
Chemical Name: Phenol, 3-[(6,7-dimethoxy-4-quinazolinyl)amino]-
CAS Number: 211555-08-7
Product Number: AG006Z3B(AGN-PC-0JK7C2)
Synonyms:
MDL No: MFCD09026915
Molecular Formula: C16H15N3O3
Molecular Weight: 297.3086

Identification/Properties

Computed Properties
Molecular Weight:
297.314g/mol
XLogP3:
3
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
6
Rotatable Bond Count:
4
Exact Mass:
297.111g/mol
Monoisotopic Mass:
297.111g/mol
Topological Polar Surface Area:
76.5A^2
Heavy Atom Count:
22
Formal Charge:
0
Complexity:
358
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

NMR Spectrum

Other Analytical Data

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Chemical Structure


WHI-P180 is a potent and selective inhibitor that has gained significant attention in the field of chemical synthesis. This compound is known for its ability to target specific enzymes or proteins involved in various chemical reactions, making it a valuable tool for researchers and chemists alike.In chemical synthesis, WHI-P180 is commonly used to disrupt specific signaling pathways or biochemical processes that are crucial for the desired reaction to occur. By inhibiting the activity of key enzymes or proteins, this compound can help researchers control the outcome of a reaction and achieve the desired product with high precision and efficiency.Furthermore, WHI-P180's selective nature allows for targeted inhibition, minimizing off-target effects and increasing the specificity of the reaction. This enables chemists to fine-tune their synthetic processes, leading to improved yields and purity of the final product.Overall, the application of WHI-P180 in chemical synthesis holds great promise for advancing the field of organic chemistry and pharmaceutical development. Its selective inhibitory properties offer a powerful tool for controlling and manipulating complex chemical reactions, making it an invaluable asset for researchers seeking to explore new frontiers in synthesis.