Methyl [1-(2-furoyl)piperidin-4-YL]acetate

Base Information

Chemical Name:Methyl [1-(2-furoyl)piperidin-4-YL]acetate
CAS No.:952934-82-6
Molecular Formula:C₁₃H₁₇NO₄
Molecular Weight:251.282
Hs Code.:
DSSTox Substance ID:DTXSID501237247
Mol file:952934-82-6.mol

Synonyms:952934-82-6;METHYL [1-(2-FUROYL)PIPERIDIN-4-YL]ACETATE;methyl 2-[1-(furan-2-carbonyl)piperidin-4-yl]acetate;Methyl 2-(1-(furan-2-carbonyl)piperidin-4-yl)acetate;DTXSID501237247;MFCD13248772;STL089948;AKOS005173730;SB61487;LS-04089;CS-0325633;Methyl 1-(2-furanylcarbonyl)-4-piperidineacetate;methyl [1-(furan-2-ylcarbonyl)piperidin-4-yl]acetate;Methyl2-(1-(furan-2-carbonyl)piperidin-4-yl)acetate;METHYL 2-[1-(2-FURYLCARBONYL)-4-PIPERIDYL]ACETATE

Suppliers and Price of Methyl [1-(2-furoyl)piperidin-4-YL]acetate

Supply Marketing:

Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

Manufacturers and distributors:

Manufacture/Brand
Chemicals and raw materials
Packaging
price

Matrix Scientific
Methyl [1-(2-furoyl)piperidin-4-yl]acetate
500mg
$ 315.00

Crysdot
Methyl2-(1-(furan-2-carbonyl)piperidin-4-yl)acetate 97%
5g
$ 904.00

Crysdot
Methyl2-(1-(furan-2-carbonyl)piperidin-4-yl)acetate 97%
1g
$ 320.00

Total 3 raw suppliers

Chemical Property of Methyl [1-(2-furoyl)piperidin-4-YL]acetate

Chemical Property:

XLogP3:1.3
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:4
Rotatable Bond Count:4
Exact Mass:251.11575802
Heavy Atom Count:18
Complexity:310

Purity/Quality:

98%min ^*data from raw suppliers

Methyl [1-(2-furoyl)piperidin-4-yl]acetate ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Canonical SMILES:COC(=O)CC1CCN(CC1)C(=O)C2=CC=CO2

Technology Process of Methyl [1-(2-furoyl)piperidin-4-YL]acetate

There total 1 articles about Methyl [1-(2-furoyl)piperidin-4-YL]acetate which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield:

: 527-69-5
2-furancarbonyl chloride

: 168986-49-0
4-piperidine acetic acid methyl ester

: 952934-82-6
C₁₃H₁₇NO₄

Guidance literature:: With N-ethyl-N,N-diisopropylamine; In dichloromethane; for 2h;
DOI:10.1016/j.bmcl.2011.07.043

Reference yield:

: 952934-82-6
C₁₃H₁₇NO₄

: C₁₉H₂₀N₂O₅

Guidance literature:: Multi-step reaction with 2 steps

1: water; lithium hydroxide / tetrahydrofuran; methanol / 20 °C

2: pyridine; triphenyl phosphite / 0.17 h / 150 °C / Microwave irradiation

With pyridine; triphenyl phosphite; water; lithium hydroxide; In tetrahydrofuran; methanol;
DOI:10.1016/j.bmcl.2011.07.043

Reference yield:

: 952934-82-6
C₁₃H₁₇NO₄

: 1333248-36-4
3-(2-ethoxyphenyl)-2-((1-(furan-2-carbonyl)piperidin-4-yl)methyl)quinazolin-4(3H)-one

Guidance literature:: Multi-step reaction with 3 steps

1: water; lithium hydroxide / tetrahydrofuran; methanol / 20 °C

2: pyridine; triphenyl phosphite / 0.17 h / 150 °C / Microwave irradiation

3: pyridine; triphenyl phosphite / 0.08 h / 230 °C / Microwave irradiation

With pyridine; triphenyl phosphite; water; lithium hydroxide; In tetrahydrofuran; methanol;
DOI:10.1016/j.bmcl.2011.07.043