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  2. Cyclopropaneacetic acid,1-[[[1-[3-[2-(7-chloro-2-quinolinyl)ethenyl]phenyl]-3-hydroxy-3-[2-(1-hydroxy-1-methylethyl)phenyl]propyl]thio]methyl]-, [R-[R*,R*-(E)]]-

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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)-

Cyclopropaneacetic acid,1-[[[1-[3-[2-(7-chloro-2-quinolinyl)ethenyl]phenyl]-3-hydroxy-3-[2-(1-hydroxy-1-methylethyl)phenyl]propyl]thio]methyl]-, [R-[R*,R*-(E)]]-

OC(=O)CC1(CS[C@@H](c2cccc(c2)/C=C/c2ccc3c(n2)cc(cc3)Cl)C[C@H](c2ccccc2C(O)(C)C)O)CC1 Request for Quotation
Chemical Name: Cyclopropaneacetic acid,1-[[[1-[3-[2-(7-chloro-2-quinolinyl)ethenyl]phenyl]-3-hydroxy-3-[2-(1-hydroxy-1-methylethyl)phenyl]propyl]thio]methyl]-, [R-[R*,R*-(E)]]-
CAS Number: 184763-26-6
Product Number: AG007S00(AGN-PC-0QDLKJ)
Synonyms:
MDL No:
Molecular Formula: C35H36ClNO4S
Molecular Weight: 602.1826

Identification/Properties

Computed Properties
Molecular Weight:
602.186g/mol
XLogP3:
6.6
Hydrogen Bond Donor Count:
3
Hydrogen Bond Acceptor Count:
6
Rotatable Bond Count:
12
Exact Mass:
601.205g/mol
Monoisotopic Mass:
601.205g/mol
Topological Polar Surface Area:
116A^2
Heavy Atom Count:
42
Formal Charge:
0
Complexity:
925
Isotope Atom Count:
0
Defined Atom Stereocenter Count:
2
Undefined Atom Stereocenter Count:
0
Defined Bond Stereocenter Count:
1
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


21(R)-Hydroxy Montelukast is a versatile compound that finds extensive application in chemical synthesis processes. Chemists utilize this compound as a key intermediate in the synthesis of various pharmaceuticals and biologically active molecules. Its unique molecular structure allows for efficient derivatization and modification, making it an essential building block in the creation of complex organic molecules. By incorporating 21(R)-Hydroxy Montelukast into synthetic routes, chemists can access new chemical entities with enhanced pharmacological properties and potential therapeutic benefits. In summary, the role of 21(R)-Hydroxy Montelukast in chemical synthesis is pivotal for the development of novel pharmaceutical compounds and the advancement of medicinal chemistry research.