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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)-

(S)-Piperidin-3-ylmethanol hydrochloride

OC[C@H]1CCCNC1.Cl Request for Quotation
Chemical Name: (S)-Piperidin-3-ylmethanol hydrochloride
CAS Number: 1125551-75-8
Product Number: AG008UAA(AGN-PC-0WAGAN)
Synonyms:
MDL No:
Molecular Formula: C6H14ClNO
Molecular Weight: 151.6345

Identification/Properties

Safety Information

GHS Pictogram:
Signal Word:
Warning
UN#:
N/A
Hazard Statements:
H302-H315-H319-H335
Precautionary Statements:
P261-P305+P351+P338
Class:
N/A
Packing Group:
N/A

NMR Spectrum

Other Analytical Data

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Chemical Structure


(S)-Piperidin-3-ylmethanol hydrochloride, a versatile compound in chemical synthesis, demonstrates exceptional reactivity and selectivity in a wide range of applications. As a chiral building block, it plays a crucial role in the synthesis of complex organic molecules and pharmaceuticals. With its unique stereochemistry, (S)-Piperidin-3-ylmethanol hydrochloride enables the creation of intricate molecular structures with high precision and efficiency. Its use in asymmetric catalysis and stereoselective transformations highlights its significance in modern synthetic chemistry. Additionally, this compound serves as a valuable intermediate in the preparation of biologically active compounds, making it an indispensable tool for researchers and synthetic chemists striving to develop novel chemical entities.