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  2. 3,4,5-Piperidinetriol, 1-butyl-2-(hydroxymethyl)-, (2R,3S,4R,5S)-

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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)-

3,4,5-Piperidinetriol, 1-butyl-2-(hydroxymethyl)-, (2R,3S,4R,5S)-

CCCCN1C[C@H](O)[C@H]([C@H]([C@H]1CO)O)O Request for Quotation
Chemical Name: 3,4,5-Piperidinetriol, 1-butyl-2-(hydroxymethyl)-, (2R,3S,4R,5S)-
CAS Number: 141206-42-0
Product Number: AG009DYX(AGN-PC-0O258J)
Synonyms:
MDL No: MFCD00269939
Molecular Formula: C10H21NO4
Molecular Weight: 219.2780

Identification/Properties

Computed Properties
Molecular Weight:
219.281g/mol
XLogP3:
-0.6
Hydrogen Bond Donor Count:
4
Hydrogen Bond Acceptor Count:
5
Rotatable Bond Count:
4
Exact Mass:
219.147g/mol
Monoisotopic Mass:
219.147g/mol
Topological Polar Surface Area:
84.2A^2
Heavy Atom Count:
15
Formal Charge:
0
Complexity:
190
Isotope Atom Count:
0
Defined Atom Stereocenter Count:
4
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


N-(n-Butyl)deoxygalactonojirimycin is a versatile compound that finds wide application in chemical synthesis. This compound is particularly valued for its crucial role as a glycosidase inhibitor. In chemical synthesis, N-(n-Butyl)deoxygalactonojirimycin can be utilized as a key building block for the creation of various bioactive molecules and pharmaceuticals.Its ability to inhibit glycosidase enzymes makes it a valuable tool in carbohydrate chemistry and chemoenzymatic synthesis. By modulating glycosidase activity, N-(n-Butyl)deoxygalactonojirimycin can facilitate the selective modification of complex carbohydrates, allowing chemists to design and synthesize new compounds with precision and efficiency.Furthermore, this compound's unique structure and reactivity make it a valuable component in the synthesis of glycosylated natural products and carbohydrate-based materials. Its application in chemical synthesis extends to the development of novel drug candidates, bioconjugates, and functionalized carbohydrates for various biomedical and biotechnological applications.