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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)-3-Amino-1-methylpiperidin-2-one hydrochloride

O=C1[C@@H](N)CCCN1C.Cl Request for Quotation
Chemical Name: (S)-3-Amino-1-methylpiperidin-2-one hydrochloride
CAS Number: 956109-56-1
Product Number: AG00H8R5(AGN-PC-0WAHW2)
Synonyms:
MDL No:
Molecular Formula: C6H13ClN2O
Molecular Weight: 164.6332

Identification/Properties

Properties
Storage:
Keep in dry area;Room Temperature;
Form:
Solid
Computed Properties
Molecular Weight:
164.633g/mol
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
2
Rotatable Bond Count:
0
Exact Mass:
164.072g/mol
Monoisotopic Mass:
164.072g/mol
Topological Polar Surface Area:
46.3A^2
Heavy Atom Count:
10
Formal Charge:
0
Complexity:
124
Isotope Atom Count:
0
Defined Atom Stereocenter Count:
1
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-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)-3-Amino-1-methylpiperidin-2-one hydrochloride, also known as $name$, is a key intermediate in chemical synthesis processes. Its versatile application lies in its role as a chiral building block, particularly in the synthesis of pharmaceutical compounds. This compound serves as a crucial starting material in the manufacture of various advanced pharmaceutical products due to its stereochemical properties. By incorporating (S)-3-Amino-1-methylpiperidin-2-one hydrochloride into chemical reactions, chemists can introduce chirality and enhance the overall selectivity and efficacy of the final products. Its strategic use in chemical synthesis allows for the creation of complex molecules with specific biological activities, making it a valuable tool in the pharmaceutical industry.