3-Piperidinecarboxylic acid, 1-methyl-, methyl ester


Chemical Name: 3-Piperidinecarboxylic acid, 1-methyl-, methyl ester
CAS Number: 1690-72-8
Product Number: AG001YFX(AGN-PC-0JKCCO)
Synonyms:
MDL No:
Molecular Formula: C8H15NO2
Molecular Weight: 157.2102

Identification/Properties


Properties
BP:
79 - 80 °C at 10 mmHg
Storage:
2-8℃;Keep in dry area;
Form:
Liquid
Refractive Index:
nD25 1.4520
Computed Properties
Molecular Weight:
157.213g/mol
XLogP3:
0.6
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
2
Exact Mass:
157.11g/mol
Monoisotopic Mass:
157.11g/mol
Topological Polar Surface Area:
29.5A^2
Heavy Atom Count:
11
Formal Charge:
0
Complexity:
147
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:
Signal Word:
Warning
UN#:
N/A
Hazard Statements:
H315-H319-H335
Precautionary Statements:
P261-P305+P351+P338
Class:
N/A
Packing Group:
N/A

NMR Spectrum


PNMR/methyl_1-methylpiperidine-3-carboxylate-1690-72-8-HNMR.pdf

Other Analytical Data


POTHER/methyl_1-methylpiperidine-3-carboxylate-1690-72-8-GC.pdf

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Chemical Structure



Methyl 1-methylpiperidine-3-carboxylate is a versatile compound widely used in chemical synthesis. In the field of organic chemistry, this compound serves as a crucial building block for the creation of various pharmaceuticals, agrochemicals, and specialty chemicals. Its unique structure and reactivity make it a valuable intermediate in the production of complex molecules.One key application of Methyl 1-methylpiperidine-3-carboxylate is in the synthesis of pharmaceutical compounds. By incorporating this compound into the molecular structure of a drug, chemists can fine-tune its biological activity, solubility, and stability. This enables the development of more effective and potent medications for treating a wide range of medical conditions.Additionally, Methyl 1-methylpiperidine-3-carboxylate is utilized in the preparation of agrochemicals, such as insecticides and herbicides. Its chemical properties allow for the synthesis of active ingredients that target specific pests or weeds while minimizing harm to the environment. This contributes to sustainable agricultural practices and helps ensure food security worldwide.Overall, the versatile nature of Methyl 1-methylpiperidine-3-carboxylate makes it an indispensable tool in chemical synthesis, enabling the creation of innovative compounds that drive advancements in various industries.