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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)-

Erythromycin, N-oxide

CC[C@H]1OC(=O)[C@H](C)[C@@H](O[C@H]2O[C@@H](C)[C@@H]([C@](C2)(C)OC)O)[C@H](C)[C@@H](O[C@@H]2O[C@H](C)C[C@@H]([C@H]2O)[N+](C)(C)[O-])[C@](C[C@H](C(=O)[C@@H]([C@H]([C@@]1(C)O)O)C)C)(C)O Request for Quotation
Chemical Name: Erythromycin, N-oxide
CAS Number: 992-65-4
Product Number: AG006ONM(AGN-PC-0W954P)
Synonyms:
MDL No:
Molecular Formula: C37H67NO14
Molecular Weight: 749.9262

Identification/Properties

Properties
MP:
215-216°C
Storage:
-10 ℃;Keep in dry area;
Form:
Solid
Computed Properties
Molecular Weight:
749.936g/mol
XLogP3:
2.7
Hydrogen Bond Donor Count:
5
Hydrogen Bond Acceptor Count:
14
Rotatable Bond Count:
7
Exact Mass:
749.456g/mol
Monoisotopic Mass:
749.456g/mol
Topological Polar Surface Area:
209A^2
Heavy Atom Count:
52
Formal Charge:
0
Complexity:
1220
Isotope Atom Count:
0
Defined Atom Stereocenter Count:
18
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


The compound $name$ ($chemical structure provided) has applications in chemical synthesis as a key intermediate in the production of pharmaceutical compounds. Its unique stereochemistry and functional groups make it valuable for constructing complex molecular structures efficiently and selectively. This compound plays a crucial role in the synthesis of biologically active molecules, enabling the creation of novel drugs and therapeutic agents through strategic chemical transformations. Its specific arrangement of atoms and bonds allows for precise manipulation in synthetic pathways, making it an essential building block in the pharmaceutical industry.