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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-Methylpiperidin-3-ol hydrochloride

CC1(O)CCCNC1.Cl Request for Quotation
Chemical Name: 3-Methylpiperidin-3-ol hydrochloride
CAS Number: 955028-98-5
Product Number: AG00IJ5T(AGN-PC-0WD4NN)
Synonyms:
MDL No: MFCD17171256
Molecular Formula: C6H14ClNO
Molecular Weight: 151.6345

Identification/Properties

Safety Information

GHS Pictogram:
N/A
Signal Word:
UN#:
-
Hazard Statements:
-
Precautionary Statements:
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

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Chemical Structure


3-Methylpiperidin-3-ol hydrochloride, also known as 3-Methyl-3-piperidinol hydrochloride, serves as a valuable building block in chemical synthesis due to its versatile reactivity and structural features. This compound is particularly utilized in the synthesis of pharmaceuticals, agrochemicals, and specialty chemicals.In chemical synthesis, 3-Methylpiperidin-3-ol hydrochloride plays a crucial role as a key intermediate in the preparation of various biologically active compounds. Its unique chemical structure provides a favorable platform for diverse functional group manipulations, enabling the synthesis of complex molecules with precision. The hydrochloride salt form enhances the compound's solubility and stability in aqueous and polar organic solvents, making it an ideal choice for reactions requiring mild acidic conditions.Furthermore, the presence of a methyl group on the piperidine ring confers specific stereochemical properties to the molecule, influencing the regioselectivity and stereoselectivity of subsequent reactions. This structural feature opens up possibilities for tailored modifications and facilitates the construction of chiral centers in target molecules.Overall, 3-Methylpiperidin-3-ol hydrochloride serves as a versatile and valuable reagent in chemical synthesis, offering chemists a strategic tool for the efficient and controlled construction of complex molecules across various industries.