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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)-

Vidupiprant, AMG 853;2-(4-(4-(tert-butylcarbamoyl)-2-(2-chloro-4-cyclopropylphenylsulfonamido)phenoxy)-5-chloro-2-fluorophenyl)acetic acid

OC(=O)Cc1cc(Cl)c(cc1F)Oc1ccc(cc1NS(=O)(=O)c1ccc(cc1Cl)C1CC1)C(=O)NC(C)(C)C Request for Quotation
Chemical Name: Vidupiprant, AMG 853;2-(4-(4-(tert-butylcarbamoyl)-2-(2-chloro-4-cyclopropylphenylsulfonamido)phenoxy)-5-chloro-2-fluorophenyl)acetic acid
CAS Number: 1169483-24-2
Product Number: AG0097ZF(AGN-PC-0WALNB)
Synonyms:
MDL No:
Molecular Formula: C28H27Cl2FN2O6S
Molecular Weight: 609.4932

Identification/Properties

Computed Properties
Molecular Weight:
609.49g/mol
XLogP3:
6
Hydrogen Bond Donor Count:
3
Hydrogen Bond Acceptor Count:
8
Rotatable Bond Count:
10
Exact Mass:
608.095g/mol
Monoisotopic Mass:
608.095g/mol
Topological Polar Surface Area:
130A^2
Heavy Atom Count:
40
Formal Charge:
0
Complexity:
1020
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


AMG 853 is a versatile chemical compound widely utilized in various applications within the field of chemical synthesis. Its unique structure and properties make it an essential component in the creation of complex organic molecules. In particular, AMG 853 is utilized as a key building block in the synthesis of pharmaceutical compounds, agrochemicals, and advanced materials.One of the prominent applications of AMG 853 in chemical synthesis is its use as a reagent for selective functional group transformations. Due to its reactive nature, AMG 853 can facilitate the conversion of functional groups within a molecule, allowing for the introduction of new chemical moieties or the modification of existing ones. This versatility makes AMG 853 an invaluable tool for chemists seeking to tailor the properties of organic compounds for specific applications.Additionally, AMG 853 is often employed as a catalyst in various synthetic reactions, promoting the formation of bonds between different molecules and driving complex transformations with high efficiency and selectivity. Its catalytic properties enable chemists to streamline the synthesis of intricate molecular structures, ultimately facilitating the development of novel compounds with tailored properties and functions.Overall, AMG 853 plays a crucial role in advancing the field of chemical synthesis by enabling the efficient construction of complex molecules and facilitating the exploration of new chemical reactions and methodologies. Its applications extend across various industries, driving innovation and discovery in the realm of organic chemistry.