1. Home
  2. NVP-HSP990(HSP990)

Contact Angene

Tel: +852 8191 6999

Email: [email protected]

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)-

NVP-HSP990(HSP990)

COc1cccc(n1)c1cc(F)ccc1[C@@H]1NC(=O)c2c(C1)nc(nc2C)N Request for Quotation
Chemical Name: NVP-HSP990(HSP990)
CAS Number: 934343-74-5
Product Number: AG00GU51(AGN-PC-0WAEPN)
Synonyms:
MDL No:
Molecular Formula: C20H18FN5O2
Molecular Weight: 379.3876

Identification/Properties

Computed Properties
Molecular Weight:
379.395g/mol
XLogP3:
2.1
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
7
Rotatable Bond Count:
3
Exact Mass:
379.144g/mol
Monoisotopic Mass:
379.144g/mol
Topological Polar Surface Area:
103A^2
Heavy Atom Count:
28
Formal Charge:
0
Complexity:
567
Isotope Atom Count:
0
Defined Atom Stereocenter Count:
1
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

Request for Quotation

Customer Feedback

Chemical Structure


The compound (7R)-2-Amino-7-[4-fluoro-2-(6-methoxy-2-pyridinyl)phenyl]-7,8-dihydro-4-methylpyrido[4,3-d]pyrimidin-5(6H)-one, when used in chemical synthesis, serves as a valuable building block for the creation of novel pharmaceutical agents and bioactive compounds. Its unique structural features make it a versatile intermediate in the synthesis of various drug candidates and organic molecules with potential therapeutic applications. By incorporating this compound into synthetic pathways, chemists can access diverse chemical space and explore the development of new drugs with enhanced biological activities.