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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)-Methyl 2-(piperidin-3-yl)acetate hydrochloride

COC(=O)C[C@@H]1CCCNC1.Cl Request for Quotation
Chemical Name: (S)-Methyl 2-(piperidin-3-yl)acetate hydrochloride
CAS Number: 957471-98-6
Product Number: AG005YCJ(AGN-PC-0WAI4H)
Synonyms:
MDL No:
Molecular Formula: C8H16ClNO2
Molecular Weight: 193.6711

Identification/Properties

Properties
Storage:
Keep in dry area;Room Temperature;
Computed Properties
Molecular Weight:
193.671g/mol
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
3
Exact Mass:
193.087g/mol
Monoisotopic Mass:
193.087g/mol
Topological Polar Surface Area:
38.3A^2
Heavy Atom Count:
12
Formal Charge:
0
Complexity:
136
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#:
-
Hazard Statements:
H302-H315-H319-H335
Precautionary Statements:
P261-P305+P351+P338
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

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Chemical Structure


The (S)-Methyl 2-(piperidin-3-yl)acetate hydrochloride is a crucial reagent in chemical synthesis due to its versatile applications. It serves as a valuable building block in the construction of various compounds through organic synthesis processes. This compound is particularly useful in the pharmaceutical industry for the creation of potential drug candidates and medicinal compounds. Its chiral nature allows for precise control over stereochemistry, making it an essential component in asymmetric synthesis. Additionally, (S)-Methyl 2-(piperidin-3-yl)acetate hydrochloride can be employed in the synthesis of complex natural products and bioactive molecules, highlighting its significance in modern chemical research and development.