4-(Boc-aMinoMethyl)-4-Methylpiperidine hydrochloride

Base Information

Chemical Name:4-(Boc-aMinoMethyl)-4-Methylpiperidine hydrochloride
CAS No.:1158759-03-5
Molecular Formula:C12H25ClN2O2
Molecular Weight:228.335
Hs Code.:
Mol file:1158759-03-5.mol

Synonyms:4-(Boc-aMinoMethyl)-4-Methylpiperidine hydrochloride;tert-butyl (4-methylpiperidin-4-yl)methylcarbamate;tert-butyl N-[(4-methylpiperidin-4-yl)methyl]carbamate

Suppliers and Price of 4-(Boc-aMinoMethyl)-4-Methylpiperidine hydrochloride

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

SynQuest Laboratories
4-(Boc-aminomethyl)-4-methylpiperidine hydrochloride
1 g
$ 825.00

SynQuest Laboratories
4-(Boc-aminomethyl)-4-methylpiperidine hydrochloride
250 mg
$ 260.00

Matrix Scientific
4-(Boc-aminomethyl)-4-methylpiperidine hydrochloride
1g
$ 983.00

Crysdot
tert-Butyl((4-methylpiperidin-4-yl)methyl)carbamate 95+%
1g
$ 1220.00

Crysdot
tert-Butyl((4-methylpiperidin-4-yl)methyl)carbamate 95+%
5g
$ 2480.00

Chemenu
tert-butylN-[(4-methylpiperidin-4-yl)methyl]carbamate 95%
5g
$ 1720.00

Ambeed
tert-Butyl((4-methylpiperidin-4-yl)methyl)carbamate 95%
250mg
$ 87.00

Ambeed
tert-Butyl((4-methylpiperidin-4-yl)methyl)carbamate 95%
100mg
$ 50.00

Ambeed
tert-Butyl((4-methylpiperidin-4-yl)methyl)carbamate 95%
1g
$ 217.00

Ambeed
tert-Butyl((4-methylpiperidin-4-yl)methyl)carbamate 95%
5g
$ 775.00

Total 16 raw suppliers

Chemical Property of 4-(Boc-aMinoMethyl)-4-Methylpiperidine hydrochloride

Chemical Property:

Boiling Point:325.7±15.0 °C(Predicted)
PKA:12.72±0.46(Predicted)
PSA：50.36000
Density:0.964±0.06 g/cm3(Predicted)
LogP:2.62050
Storage Temp.:2-8°C(protect from light)

Purity/Quality:

97% ^*data from raw suppliers

4-(Boc-aminomethyl)-4-methylpiperidine hydrochloride ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Technology Process of 4-(Boc-aMinoMethyl)-4-Methylpiperidine hydrochloride

There total 8 articles about 4-(Boc-aMinoMethyl)-4-Methylpiperidine hydrochloride 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%

: 1345728-58-6
tert-butyl [(1-benzyl-4-methylpiperidin-4-yl)methyl]carbamate

: 1158759-03-5
tert-butyl N-[(4-methylpiperidin-4-yl)methyl]carbamate

Guidance literature:: With palladium 10% on activated carbon; hydrogen; In methanol; at 20 ℃; for 3h;

Reference yield: 70.5%

: tert-butyl 1-benzoyl-((4-methylpiperidin-4-yl)methyl)carbamate

: 1158759-03-5
tert-butyl N-[(4-methylpiperidin-4-yl)methyl]carbamate

Guidance literature:: With sodium hydroxide; In ethanol; at 90 ℃; for 8h; Inert atmosphere;

Reference yield:

: 1345728-57-5
1-benzyl-4-methylpiperidine-4-carboxamide

: 1158759-03-5
tert-butyl N-[(4-methylpiperidin-4-yl)methyl]carbamate

Guidance literature:: Multi-step reaction with 3 steps

1: lithium aluminium tetrahydride / tetrahydrofuran / 2.5 h / 50 °C / Cooling with ice; Inert atmosphere

2: tetrahydrofuran / 16 h / 20 °C

3: 20% palladium hydroxide-activated charcoal; hydrogen / ethanol / 16 h / 70 °C / 2250.23 Torr

With lithium aluminium tetrahydride; 20% palladium hydroxide-activated charcoal; hydrogen; In tetrahydrofuran; ethanol;