methyl 4-piperidinecarboxylate

Basic information

  • Product Name:methyl 4-piperidinecarboxylate
  • CasNo.:2971-79-1
  • MF:C7H13NO2

Physical and Chemical Properties

  • Purity:99%
  • Melting Point:50oC
  • Appearance:White to off-white crysrallic powder
Inquiry

Product Details

CasNo: 2971-79-1

MF: C7H13NO2

Appearance: White to off-white crysrallic powder

Factory Export Top Purity methyl 4-piperidinecarboxylate 2971-79-1 In Stock

  • Molecular Formula:C7H13NO2
  • Molecular Weight:143.186
  • Appearance/Colour:White to off-white crysrallic powder 
  • Vapor Pressure:0.457mmHg at 25°C 
  • Melting Point:50oC 
  • Refractive Index:1.465 
  • Boiling Point:193.8 °C at 760 mmHg 
  • PKA:9.78±0.10(Predicted) 
  • Flash Point:71 °C 
  • PSA:42.91000 
  • Density:1.021 g/cm3 
  • LogP:0.70200 

methyl 4-piperidinecarboxylate(Cas 2971-79-1) Usage

Methyl 4-piperidinecarboxylate is a colorless to pale yellow liquid that serves as an important intermediate in organic synthesis. As a derivative of piperidine characterized by a carboxylic acid ester group attached to the fourth carbon of the piperidine ring, it typically appears as a clear liquid. This compound is synthesized through specific chemical reactions, such as the esterification of 4-piperidinecarboxylic acid with methanol under suitable conditions. Methyl 4-piperidinecarboxylate finds applications in drug development, pesticide synthesis, and materials science. In drug synthesis, it may act as a key structural unit for molecules with specific pharmacological activity, particularly those targeting the central nervous system. Additionally, it plays a role in the production of agrochemicals and other specialized chemicals, making it a versatile component in various industries.

 

InChI:InChI=1/C7H13NO2/c1-10-7(9)6-2-4-8-5-3-6/h6,8H,2-5H2,1H3

2971-79-1 Relevant articles

Synthesis and biological evaluation of 4-piperidinecarboxylate and 4-piperidinecyanide derivatives for T-type calcium channel blockers

Harris,Nation,Copeland,Miller

, Bioorganic & Medicinal Chemistry Letters Volume 21, Issue 19 , 1 October 2011, Pages 5910-5915

To obtain selective and potent inhibitor for T-type calcium channel by ligand based drug design, 4-piperidinecarboxylate and 4-piperidinecyanide derivatives were prepared and evaluated for in vitro and in vivo activity against α1G calcium channel. Among them, several compounds showed good T-type calcium channel inhibitory activity and minimal off-target activity over hERG channel (% inhibition at 10 μM = 61.85–71.99, hERG channel IC50 = 1.57 ± 0.14–4.98 ± 0.36 μM). Selected compound 31a was evaluated on SNL model of neuropathic pain and showed inhibitory effect on mechanical allodynia.

The face selectivity of 1,3-dipolar cycloaddition reactions of 4-butyloxycarbonyl-3,4,5,6-tetrahydropyridine 1-oxide

Alsbaiee, Alaaeddin,Ali, Shaikh A.

, p. 6635 - 6644 (2008)

A study of the stereo- and face selectiv...

Design, synthesis and anticancer activities of novel dual poly(ADP-ribose) polymerase-1/histone deacetylase-1 inhibitors

Liao, Chenzhong,Tian, Yongbin,Xie, Zhouling

supporting information, (2020/02/27)

Currently, synergistic inhibition of pol...

2971-79-1 Process route

N-tritylisonipecotic acid methyl ester
1262670-73-4

N-tritylisonipecotic acid methyl ester

isonipecotic acid methyl ester
2971-79-1

isonipecotic acid methyl ester

Conditions
Conditions Yield
With ammonium cerium (IV) nitrate; water; acetic acid; In dichloromethane; at 20 ℃; for 1h; Inert atmosphere;
89%
methanol
67-56-1

methanol

isonipecotic acid
498-94-2

isonipecotic acid

isonipecotic acid methyl ester
2971-79-1

isonipecotic acid methyl ester

Conditions
Conditions Yield
With thionyl chloride; at 0 ℃; Reflux;
99%
With hydrogenchloride; for 4h;
70%
With thionyl chloride;
 
With thionyl chloride; for 1h; Heating;
 
With hydrogenchloride; for 3h; Heating;
 
With thionyl chloride; at 20 ℃;
 
With thionyl chloride; at 0 - 20 ℃; for 18h;
 
With thionyl chloride; at 0 - 20 ℃; for 18h;
 
With thionyl chloride; at 0 - 20 ℃; for 18h;
 
With sulfuryl dichloride; at 20 - 50 ℃;
 
With thionyl chloride; at 0 - 20 ℃; for 18h;
 
With thionyl chloride; In methanol; at 0 - 25 ℃; for 12h;
 
With thionyl chloride; at 0 ℃; for 1h; Inert atmosphere; Reflux;
 

2971-79-1 Upstream products

  • 498-94-2
    498-94-2

    isonipecotic acid

  • 2459-09-8
    2459-09-8

    4-pyridinecarboxylic acid, methyl ester

  • 67-56-1
    67-56-1

    methanol

  • 84358-13-4
    84358-13-4

    N-[(tert-butoxy)carbonyl]piperidine-4-carboxylic acid

2971-79-1 Downstream products

  • 1690-75-1
    1690-75-1

    1-methyl-piperidine-4-carboxylic acid methyl ester

  • 126291-66-5
    126291-66-5

    1-acetyl-piperidine-4-carboxylic acid methyl ester

  • 10315-06-7
    10315-06-7

    1-benzylpiperidine-4-carboxylic acid methyl ester