(R)-tert-butyl 1-(ethylamino)propan-2-ylcarbamate

Base Information

Chemical Name:(R)-tert-butyl 1-(ethylamino)propan-2-ylcarbamate
CAS No.:869901-70-2
Molecular Formula:C₁₀H₂₂N₂O₂
Molecular Weight:202.297
Hs Code.:
Mol file:869901-70-2.mol

Synonyms:tert-butyl[(1S)-2-(ethylamino)-1-methylethyl]carbamate;tert-butyl(trimethylstannyl)amine;Stannanamine,N-(1,1-dimethylethyl)-1,1,1-trimethyl;

Suppliers and Price of (R)-tert-butyl 1-(ethylamino)propan-2-ylcarbamate

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
(R)-tert-Butyl(1-(ethylamino)propan-2-yl)carbamate 95+%
1g
$ 455.00

American Custom Chemicals Corporation
(R)-TERT-BUTYL-(1-(ETHYLAMINO)PROPAN-2-YL)CARBAMATE 95.00%
5MG
$ 497.93

Total 13 raw suppliers

Chemical Property of (R)-tert-butyl 1-(ethylamino)propan-2-ylcarbamate

Chemical Property:

PSA：53.85000
LogP:2.10440
Storage Temp.:2-8°C

Purity/Quality:

97% ^*data from raw suppliers

(R)-tert-Butyl(1-(ethylamino)propan-2-yl)carbamate 95+% ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Technology Process of (R)-tert-butyl 1-(ethylamino)propan-2-ylcarbamate

There total 3 articles about (R)-tert-butyl 1-(ethylamino)propan-2-ylcarbamate 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:

: 557-66-4
ethanamine hydrochloride

: 79069-50-4
Boc-Ala-H

: 869901-70-2
tert-butyl[(1S)-2-(ethylamino)-1-methylethyl]carbamate

Guidance literature:: With sodium tris(acetoxy)borohydride; In methanol; at 0 - 20 ℃;

Reference yield:

: 126257-76-9
(S)-2-(tert-butoxycarbonylamino)-N-ethylpropanamide

: 869901-70-2
tert-butyl[(1S)-2-(ethylamino)-1-methylethyl]carbamate

Guidance literature:: With sodium bis(2-methoxyethoxy)aluminium dihydride; In tetrahydrofuran; toluene; at 35 ℃; for 17h;
DOI:10.1016/j.tetlet.2006.01.056

Reference yield:

: 15761-38-3
L-N-Boc-Ala

: 869901-70-2
tert-butyl[(1S)-2-(ethylamino)-1-methylethyl]carbamate

Guidance literature:: Multi-step reaction with 2 steps

1: N-methylmorpholine; i-butylchloroformate / tetrahydrofuran / -15 °C

2: sodium bis(2-methoxyethoxy) aluminium hydride / toluene; tetrahydrofuran / 17 h / 35 °C

With 4-methyl-morpholine; sodium bis(2-methoxyethoxy)aluminium dihydride; isobutyl chloroformate; In tetrahydrofuran; toluene;
DOI:10.1016/j.tetlet.2006.01.056