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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)-

PSB 36

OCCCn1c2nc([nH]c2c(=O)n(c1=O)CCCC)C12CC3CC2CC(C1)C3 Request for Quotation
Chemical Name: PSB 36
CAS Number: 524944-72-7
Product Number: AG00DGSE(AGN-PC-00E6Q0)
Synonyms:
MDL No: MFCD08703092
Molecular Formula: C21H30N4O3
Molecular Weight: 386.4879

Identification/Properties

Computed Properties
Molecular Weight:
386.496g/mol
XLogP3:
4
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
4
Rotatable Bond Count:
7
Exact Mass:
386.232g/mol
Monoisotopic Mass:
386.232g/mol
Topological Polar Surface Area:
89.5A^2
Heavy Atom Count:
28
Formal Charge:
0
Complexity:
642
Isotope Atom Count:
0
Defined Atom Stereocenter Count:
0
Undefined Atom Stereocenter Count:
2
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


PSB 36 is an indispensable catalyst in chemical synthesis, particularly prized for its versatility and efficiency. Its unique properties make it an ideal choice for a wide range of applications, including the production of pharmaceuticals, agrochemicals, and specialty chemicals. With its high selectivity and excellent reactivity, PSB 36 enables precise control over reaction pathways, leading to increased yields and purity of the desired products. Additionally, its stability under a variety of reaction conditions makes it a reliable tool for chemists seeking to streamline their synthetic processes. Overall, PSB 36 is a valuable asset in the laboratory, offering chemists a powerful means to drive innovation and accelerate the development of novel compounds.