N-BENZYL-2,3,4,6-TETRA-O-BENZYL-1,5-DIDEOXY-IMINO-L-IDITOL|151963-95-0,AngeneChemical

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Pyrimidine, 5-bromo-2-methyl-

1,3,5,2,4,6-Trioxatriphosphorinane, 2,4,6-tripropyl-, 2,4,6-trioxide

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)-

N-BENZYL-2,3,4,6-TETRA-O-BENZYL-1,5-DIDEOXY-IMINO-L-IDITOL

c1ccc(cc1)CO[C@H]1C(OCc2ccccc2)[C@H](OCc2ccccc2)CN(C1COCc1ccccc1)Cc1ccccc1

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Chemical Name:	N-BENZYL-2,3,4,6-TETRA-O-BENZYL-1,5-DIDEOXY-IMINO-L-IDITOL
CAS Number:	151963-95-0
Product Number:	AG007JSU(AGN-PC-0O4BNP)
Synonyms:
MDL No:
Molecular Formula:	C41H43NO4
Molecular Weight:	613.7844

Identification/Properties
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Identification/Properties

Computed Properties

Molecular Weight:

613.798g/mol

XLogP3:

7.2

Hydrogen Bond Donor Count:

Hydrogen Bond Acceptor Count:

Rotatable Bond Count:

Exact Mass:

613.319g/mol

Monoisotopic Mass:

613.319g/mol

Topological Polar Surface Area:

40.2A^2

Heavy Atom Count:

Formal Charge:

Complexity:

794

Isotope Atom Count:

Defined Atom Stereocenter Count:

Undefined Atom Stereocenter Count:

Defined Bond Stereocenter Count:

Undefined Bond Stereocenter Count:

Covalently-Bonded Unit Count:

Compound Is Canonicalized:

Yes

Safety Information

NMR Spectrum

Other Analytical Data

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Chemical Structure

N-Benzyl-2,3,4,6-tetra-O-benzyl-1,5-dideoxy-imino-L-iditol is a versatile compound widely used in chemical synthesis. This compound is particularly valued for its ability to act as a key building block in the creation of various complex molecules and pharmaceuticals. With its unique structure and reactivity, N-Benzyl-2,3,4,6-tetra-O-benzyl-1,5-dideoxy-imino-L-iditol plays a crucial role in the preparation of carbohydrate-based compounds, glycopeptides, and glycolipids. In addition, it serves as a valuable tool in the development of new synthetic methodologies, making it an indispensable component in the realm of organic chemistry and drug discovery.