tert-Butyl (4-ethylpiperidin-4-yl)carbamate

Base Information

Chemical Name:tert-Butyl (4-ethylpiperidin-4-yl)carbamate
CAS No.:440101-15-5
Molecular Formula:C₁₂H₂₄N₂O₂
Molecular Weight:228.335
Hs Code.:2933399090
European Community (EC) Number:829-466-0
Mol file:440101-15-5.mol

Synonyms:tert-Butyl (4-ethylpiperidin-4-yl)carbamate;440101-15-5;4-Ethyl-4-N-Boc-aMinopiperidine;tert-butyl N-(4-ethylpiperidin-4-yl)carbamate;tert-butyl 4-ethylpiperidin-4-ylcarbamate;SCHEMBL6703818;FYMDORPYGXGRNV-UHFFFAOYSA-N;MFCD14582327;AT23026;SB43640;AS-76759;DA-42437;t-Butyl (4-ethylpiperidin-4-yl)carbamate;tert-Butyl(4-ethylpiperidin-4-yl)carbamate;4-tert-butoxycarbonylamino-4-ethylpiperidine;CS-0139604;EN300-381136

Suppliers and Price of tert-Butyl (4-ethylpiperidin-4-yl)carbamate

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

Crysdot
tert-Butyl(4-ethylpiperidin-4-yl)carbamate 95+%
250mg
$ 376.00

Crysdot
tert-Butyl(4-ethylpiperidin-4-yl)carbamate 95+%
1g
$ 942.00

Crysdot
tert-Butyl(4-ethylpiperidin-4-yl)carbamate 95+%
25mg
$ 118.00

Crysdot
tert-Butyl(4-ethylpiperidin-4-yl)carbamate 95+%
100mg
$ 236.00

Crysdot
tert-Butyl(4-ethylpiperidin-4-yl)carbamate 95+%
5g
$ 2867.00

Ambeed
tert-Butyl(4-ethylpiperidin-4-yl)carbamate 95%
1g
$ 395.00

Ambeed
tert-Butyl(4-ethylpiperidin-4-yl)carbamate 95%
250mg
$ 156.00

Ambeed
tert-Butyl(4-ethylpiperidin-4-yl)carbamate 95%
100mg
$ 83.00

Alichem
tert-Butyl(4-ethylpiperidin-4-yl)carbamate
250mg
$ 418.00

Alichem
tert-Butyl(4-ethylpiperidin-4-yl)carbamate
1g
$ 1007.00

Total 8 raw suppliers

Chemical Property of tert-Butyl (4-ethylpiperidin-4-yl)carbamate

Chemical Property:

PSA：53.85000
LogP:2.57650
Storage Temp.:2-8°C
XLogP3:1.8
Hydrogen Bond Donor Count:2
Hydrogen Bond Acceptor Count:3
Rotatable Bond Count:4
Exact Mass:228.183778013
Heavy Atom Count:16
Complexity:240

Purity/Quality:

97% ^*data from raw suppliers

tert-Butyl(4-ethylpiperidin-4-yl)carbamate 95+% ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CCC1(CCNCC1)NC(=O)OC(C)(C)C

Technology Process of tert-Butyl (4-ethylpiperidin-4-yl)carbamate

There total 4 articles about tert-Butyl (4-ethylpiperidin-4-yl)carbamate 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: 94.0%

: 1-benzyl-4-tert-butoxycarbonylamino-4-ethylpiperidine

: 440101-15-5
tert-butyl (4-ethylpiperidin-4-yl)carbamate

Guidance literature:: With hydrogen; palladium 10% on activated carbon; In ethanol; water; for 48h; under 760.051 Torr;

Reference yield:

: 10315-06-7
1-benzylpiperidine-4-carboxylic acid methyl ester

: 440101-15-5
tert-butyl (4-ethylpiperidin-4-yl)carbamate

Guidance literature:: Multi-step reaction with 4 steps

1.1: lithium diisopropyl amide / tetrahydrofuran / 1 h / -78 °C / Inert atmosphere

1.2: 4 h / -78 °C / Inert atmosphere

2.1: sodium hydroxide; water / ethanol / 16 h / 10 - 30 °C

3.1: diphenyl phosphoryl azide; triethylamine / 8 h / Reflux

4.1: palladium on activated charcoal; hydrogen / methanol / 16 h / 10 - 30 °C

With diphenyl phosphoryl azide; palladium on activated charcoal; water; hydrogen; triethylamine; sodium hydroxide; lithium diisopropyl amide; In tetrahydrofuran; methanol; ethanol;

Reference yield:

: 1-benzyl-4-ethylpiperidine-4-carboxylic acid methyl ester

: 440101-15-5
tert-butyl (4-ethylpiperidin-4-yl)carbamate

Guidance literature:: Multi-step reaction with 3 steps

1: sodium hydroxide; water / ethanol / 16 h / 10 - 30 °C

2: diphenyl phosphoryl azide; triethylamine / 8 h / Reflux

3: palladium on activated charcoal; hydrogen / methanol / 16 h / 10 - 30 °C

With diphenyl phosphoryl azide; palladium on activated charcoal; water; hydrogen; triethylamine; sodium hydroxide; In methanol; ethanol;