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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)-

Urea, N-(1-benzo[b]thien-2-ylethyl)-N-hydroxy-

ON(C(c1cc2c(s1)cccc2)C)C(=O)N Request for Quotation
Chemical Name: Urea, N-(1-benzo[b]thien-2-ylethyl)-N-hydroxy-
CAS Number: 111406-87-2
Product Number: AG00HC56(AGN-PC-07A28M)
Synonyms:
MDL No:
Molecular Formula: C11H12N2O2S
Molecular Weight: 236.2902

Identification/Properties

Computed Properties
Molecular Weight:
236.289g/mol
XLogP3:
1.6
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
2
Exact Mass:
236.062g/mol
Monoisotopic Mass:
236.062g/mol
Topological Polar Surface Area:
94.8A^2
Heavy Atom Count:
16
Formal Charge:
0
Complexity:
275
Isotope Atom Count:
0
Defined Atom Stereocenter Count:
0
Undefined Atom Stereocenter Count:
1
Defined Bond Stereocenter Count:
0
Undefined Bond Stereocenter Count:
0
Covalently-Bonded Unit Count:
1
Compound Is Canonicalized:
Yes

Safety Information

GHS Pictogram:
Signal Word:
Warning
UN#:
N/A
Hazard Statements:
H302-H319-H350-H360
Precautionary Statements:
P305+P351+P338
Class:
N/A
Packing Group:
N/A

NMR Spectrum

Other Analytical Data

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Chemical Structure


Zileuton, a compound commonly utilized in chemical synthesis, is a potent inhibitor of the enzyme 5-lipoxygenase. This enzyme plays a crucial role in the biosynthesis of leukotrienes, which are inflammatory mediators involved in numerous physiological processes. By targeting 5-lipoxygenase, Zileuton effectively suppresses the production of leukotrienes, making it a valuable tool in the development of anti-inflammatory agents and pharmaceuticals. In chemical synthesis, Zileuton's ability to selectively block this specific enzyme pathway opens up opportunities for the creation of novel drug candidates and therapeutic agents that target inflammatory conditions and related disorders. Its versatile application in the field of chemical synthesis underscores Zileuton's importance as a key component in pharmaceutical research and development efforts.