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

OC[C@@H]1NC[C@@H]([C@H]([C@@H]1O)O)O.Cl Request for Quotation
Chemical Name: 3,4,5-Piperidinetriol, 2-(hydroxymethyl)-, hydrochloride, (2S,3R,4R,5S)-
CAS Number: 210223-32-8
Product Number: AG002KN3(AGN-PC-0O7QIK)
Synonyms:
MDL No:
Molecular Formula: C6H14ClNO4
Molecular Weight: 199.63266

Identification/Properties

Properties
Storage:
2-8℃;Keep in dry area;
Computed Properties
Molecular Weight:
199.63g/mol
Hydrogen Bond Donor Count:
6
Hydrogen Bond Acceptor Count:
5
Rotatable Bond Count:
1
Exact Mass:
199.061136g/mol
Monoisotopic Mass:
199.061136g/mol
Topological Polar Surface Area:
93Ų
Heavy Atom Count:
12
Formal Charge:
0
Complexity:
132
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:
2
Compound Is Canonicalized:
Yes

Safety Information

NMR Spectrum

Other Analytical Data

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Chemical Structure


1-Deoxy-L-idonojirimycin HCl, also known as DNJ, is a valuable compound widely utilized in chemical synthesis for its unique properties and versatile applications. As a potent alpha-glucosidase inhibitor, 1-Deoxy-L-idonojirimycin HCl plays a crucial role in the development of pharmaceuticals targeting conditions such as diabetes and metabolic disorders. Its ability to modulate enzyme activity makes it an essential tool in the synthesis of medicinal compounds that regulate blood sugar levels and improve metabolic function.Moreover, 1-Deoxy-L-idonojirimycin HCl is frequently employed in the synthesis of complex carbohydrates and glycoproteins. Its structural similarities to natural sugars enable it to participate in a variety of glycosylation reactions, facilitating the creation of novel glycoconjugates with enhanced bioactivity and stability.In the field of chemical biology, 1-Deoxy-L-idonojirimycin HCl serves as a valuable probe for investigating carbohydrate processing pathways and studying the mechanisms of glycosidase enzymes. Its selective inhibition of specific glycosidases allows researchers to dissect complex cellular processes and develop new strategies for targeted drug delivery and therapeutic interventions.Overall, the versatile application of 1-Deoxy-L-idonojirimycin HCl in chemical synthesis underscores its importance in advancing research and innovation across various scientific disciplines.