(S)-Tetrahydro-2H-pyran-3-amine hydrochloride

Base Information

Chemical Name:(S)-Tetrahydro-2H-pyran-3-amine hydrochloride
CAS No.:1245724-46-2
Molecular Formula:C5H12ClNO
Molecular Weight:137.609
Hs Code.:
Mol file:1245724-46-2.mol

Synonyms:(S)-Tetrahydro-2H-pyran-3-amine hydrochloride;(S)-tetrahydro-2H-pyran-3-amine;(S)-3-AMinotetrahydropyran Hydrochloride;(S)-Tetrahydro-2H-pyran-3-amine hydrochloride hydrochloride;(S)-Tetrahydro-pyran-3-ylamine;(S)-Tetrahydro-pyran-3-ylamine hydrochloride;(3S)-oxan-3-amine hydrochloride;(3S)-tetrahydro-2H-Pyran-3-amine hydrochloride

Suppliers and Price of (S)-Tetrahydro-2H-pyran-3-amine 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
(3S)-Oxan-3-amine hydrochloride
5 g
$ 750.00

SynQuest Laboratories
(3S)-Oxan-3-amine hydrochloride
1 g
$ 225.00

Total 22 raw suppliers

Chemical Property of (S)-Tetrahydro-2H-pyran-3-amine hydrochloride

Chemical Property:

PSA：35.25000
LogP:1.62640
Storage Temp.:under inert gas (nitrogen or Argon) at 2-8°C

Purity/Quality:

99%, ^*data from raw suppliers

(3S)-Oxan-3-amine hydrochloride ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Technology Process of (S)-Tetrahydro-2H-pyran-3-amine hydrochloride

There total 4 articles about (S)-Tetrahydro-2H-pyran-3-amine 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: 99.8%

: 1295722-66-5,1245648-17-2
(S)-tert-butyl (tetrahydro-2H-pyran-3-yl)carbamate

: 1245724-46-2,1315500-31-2
(S)-(tetrahydro-pyran-3-yl)amine hydrochloride

Guidance literature:: With hydrogenchloride; In methanol; at 20 ℃;

Reference yield:

: 56-86-0,21675-62-7,23009-64-5,25104-13-6,84960-48-5,25513-46-6
L-glutamic acid

: 1245724-46-2,1315500-31-2
(S)-(tetrahydro-pyran-3-yl)amine hydrochloride

Guidance literature:: Multi-step reaction with 4 steps

1.1: chloro-trimethyl-silane / 0 - 20 °C

1.2: 25 °C

2.1: lithium borohydride / tetrahydrofuran / 16 h / 0 - 20 °C

2.2: 0 °C

3.1: triphenylphosphine; di-isopropyl azodicarboxylate / dichloromethane / 48 h / 20 °C

4.1: hydrogenchloride / methanol / 20 °C

With hydrogenchloride; lithium borohydride; chloro-trimethyl-silane; di-isopropyl azodicarboxylate; triphenylphosphine; In tetrahydrofuran; methanol; dichloromethane;

Reference yield:

: 59279-60-6,130622-05-8,861658-15-3
dimethyl (2S)-2-[(tert-butoxycarbonyl)amino]pentanedioate

: 1245724-46-2,1315500-31-2
(S)-(tetrahydro-pyran-3-yl)amine hydrochloride

Guidance literature:: Multi-step reaction with 3 steps

1.1: lithium borohydride / tetrahydrofuran / 16 h / 0 - 20 °C

1.2: 0 °C

2.1: triphenylphosphine; di-isopropyl azodicarboxylate / dichloromethane / 48 h / 20 °C

3.1: hydrogenchloride / methanol / 20 °C

With hydrogenchloride; lithium borohydride; di-isopropyl azodicarboxylate; triphenylphosphine; In tetrahydrofuran; methanol; dichloromethane;