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

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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, (2R,3R,4R,5R)-

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, (2R,3R,4R,5R)-
CAS Number: 73465-43-7
Product Number: AG01CBEX(AGN-PC-0OHAEX)
Synonyms:
MDL No:
Molecular Formula: C6H14ClNO4
Molecular Weight: 199.6327

Identification/Properties

Computed Properties
Molecular Weight:
199.631g/mol
Hydrogen Bond Donor Count:
6
Hydrogen Bond Acceptor Count:
5
Rotatable Bond Count:
1
Exact Mass:
199.061g/mol
Monoisotopic Mass:
199.061g/mol
Topological Polar Surface Area:
93A^2
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

GHS Pictogram:
Signal Word:
Warning
UN#:
N/A
Hazard Statements:
H302-H312-H332
Precautionary Statements:
P280
Class:
N/A
Packing Group:
N/A

NMR Spectrum

Other Analytical Data

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Chemical Structure


The compound (2R,3R,4R,5R)-2-(Hydroxymethyl)piperidine-3,4,5-triol hydrochloride is commonly employed in chemical synthesis as a versatile building block due to its unique structure and properties. Its chiral nature, coupled with multiple hydroxyl functional groups, make it a valuable reagent for the preparation of complex organic molecules with specific stereochemistry.In chemical synthesis, this compound can serve as a key intermediate for the construction of various pharmaceuticals, natural products, and other fine chemicals. Its piperidine ring offers opportunities for diversification through functional group interconversions, while the triol functionality provides points for further modifications or derivatizations.By strategically incorporating (2R,3R,4R,5R)-2-(Hydroxymethyl)piperidine-3,4,5-triol hydrochloride into synthetic pathways, chemists can access a wide range of enantiomerically pure compounds with tailored properties and biological activities. Its presence in a synthesis can facilitate the creation of intricate molecular architectures with precise control over stereochemical outcomes.