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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-(hydroxymethyl)-1-methylpiperidin-2-one

OCC1CCCN(C1=O)C Request for Quotation
Chemical Name: 3-(hydroxymethyl)-1-methylpiperidin-2-one
CAS Number: 944276-44-2
Product Number: AG00II5J(AGN-PC-014RTD)
Synonyms:
MDL No:
Molecular Formula: C7H13NO2
Molecular Weight: 143.1836

Identification/Properties

Computed Properties
Molecular Weight:
143.186g/mol
XLogP3:
0
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
2
Rotatable Bond Count:
1
Exact Mass:
143.095g/mol
Monoisotopic Mass:
143.095g/mol
Topological Polar Surface Area:
40.5A^2
Heavy Atom Count:
10
Formal Charge:
0
Complexity:
136
Isotope Atom Count:
0
Defined Atom Stereocenter Count:
0
Undefined Atom Stereocenter Count:
1
Defined Bond Stereocenter Count:
0
Undefined Bond Stereocenter Count:
0
Covalently-Bonded Unit Count:
1
Compound Is Canonicalized:
Yes

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-(Hydroxymethyl)-1-methylpiperidin-2-one, also known as HMMP, is a versatile compound widely used in chemical synthesis. Its primary application lies in the field of medicinal chemistry. HMMP serves as a key building block for the synthesis of various pharmaceutical intermediates and active ingredients. In particular, it is utilized in the development of antiviral, antibacterial, and antifungal agents. The unique structure of HMMP allows for the introduction of functional groups at multiple sites, enabling the facile modification of its chemical properties to tailor the desired biological activity. Additionally, HMMP demonstrates excellent reactivity in a range of synthetic transformations, making it a valuable tool for the preparation of diverse molecular scaffolds. Its strategic incorporation into synthetic routes contributes to the efficient production of complex molecules with therapeutic potential. In summary, 3-(Hydroxymethyl)-1-methylpiperidin-2-one plays a crucial role in driving innovation and advancement within the realm of chemical synthesis, particularly in the development of novel pharmaceutical compounds.