1. Home
  2. INCB024360

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)-

INCB024360

ON/C(=N/c1ccc(c(c1)Cl)F)/c1nonc1N Request for Quotation
Chemical Name: INCB024360
CAS Number: 914471-09-3
Product Number: AG00GU3R(AGN-PC-0WAHUX)
Synonyms:
MDL No:
Molecular Formula: C9H7ClFN5O2
Molecular Weight: 271.6356

Identification/Properties

Computed Properties
Molecular Weight:
271.636g/mol
XLogP3:
1.6
Hydrogen Bond Donor Count:
3
Hydrogen Bond Acceptor Count:
7
Rotatable Bond Count:
3
Exact Mass:
271.027g/mol
Monoisotopic Mass:
271.027g/mol
Topological Polar Surface Area:
110A^2
Heavy Atom Count:
18
Formal Charge:
0
Complexity:
321
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

Request for Quotation

Customer Feedback

Chemical Structure


In chemical synthesis, IDO5L serves as a versatile catalyst that enables the efficient and selective transformation of a wide range of substrates. This innovative catalyst offers exceptional reactivity and high chemoselectivity, making it ideal for various synthetic pathways. By facilitating complex bond formations and enabling intricate functional group manipulations, IDO5L plays a crucial role in the synthesis of pharmaceuticals, agrochemicals, and advanced materials. Its unique properties allow chemists to streamline synthetic routes, improve overall yields, and access novel compounds that were previously challenging to synthesize. Additionally, IDO5L exhibits excellent stability and compatibility with diverse reaction conditions, making it a valuable tool for researchers in the field of organic chemistry. Whether used in cross-coupling reactions, C-H activation, or other transformations, IDO5L consistently delivers reliable results and enhances the efficiency of chemical synthesis processes.