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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)-

4-Piperidineacetic acid, 1-methyl-, methyl ester

COC(=O)CC1CCN(CC1)C Request for Quotation
Chemical Name: 4-Piperidineacetic acid, 1-methyl-, methyl ester
CAS Number: 95533-25-8
Product Number: AG0036WD(AGN-PC-02D6M9)
Synonyms:
MDL No: MFCD12756507
Molecular Formula: C9H17NO2
Molecular Weight: 171.2368

Identification/Properties

Properties
BP:
210.2°C at 760 mmHg
Storage:
Keep in dry area;2-8℃;
Computed Properties
Molecular Weight:
171.24g/mol
XLogP3:
0.8
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
3
Exact Mass:
171.126g/mol
Monoisotopic Mass:
171.126g/mol
Topological Polar Surface Area:
29.5A^2
Heavy Atom Count:
12
Formal Charge:
0
Complexity:
151
Isotope Atom Count:
0
Defined Atom Stereocenter Count:
0
Undefined Atom Stereocenter Count:
0
Defined Bond Stereocenter Count:
0
Undefined Bond Stereocenter Count:
0
Covalently-Bonded Unit Count:
1
Compound Is Canonicalized:
Yes

Safety Information

GHS Pictogram:
Signal Word:
Warning
UN#:
N/A
Hazard Statements:
H227-H315-H319-H335
Precautionary Statements:
P305+P351+P338
Class:
N/A
Packing Group:
N/A

NMR Spectrum

Other Analytical Data

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Chemical Structure


Methyl 2-(1-methylpiperidin-4-yl)acetate is a versatile compound widely used in chemical synthesis as a building block for creating various pharmaceuticals, agrochemicals, and advanced materials. This compound serves as a key intermediate in the synthesis of compounds with important biological activities. Its unique structure and reactivity make it a valuable reagent for organic chemists in the development of novel molecules with potential therapeutic benefits. In the field of medicinal chemistry, Methyl 2-(1-methylpiperidin-4-yl)acetate plays a crucial role in the synthesis of drugs targeting neurological disorders, cardiovascular diseases, and infectious diseases. Its versatility also extends to the preparation of fine chemicals and fragrances, showcasing its significance in a wide range of chemical applications. Whether used in academia or industry, this compound remains a fundamental tool for researchers seeking to explore new chemical pathways and discover innovative molecules with diverse functionalities.