TRIMETHYL (2-N-T-BUTOXYCARBONYLAMINO)ETHYLAMMONIUM BROMIDE

Base Information

Chemical Name:TRIMETHYL (2-N-T-BUTOXYCARBONYLAMINO)ETHYLAMMONIUM BROMIDE
CAS No.:945713-45-1
Molecular Formula:C₁₀H₂₃N₂O₂
Molecular Weight:203.305
Hs Code.:
Mol file:945713-45-1.mol

Synonyms:

Suppliers and Price of TRIMETHYL (2-N-T-BUTOXYCARBONYLAMINO)ETHYLAMMONIUM BROMIDE

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

TRC
Trimethyl(2-N-t-Butoxycarbonylamino)ethylammoniumBromide
50mg
$ 130.00

Medical Isotopes, Inc.
Trimethyl(2-N-t-Butoxycarbonylamino)ethylammoniumBromide
50 mg
$ 875.00

Medical Isotopes, Inc.
Trimethyl(2-N-t-Butoxycarbonylamino)ethylammoniumBromide
250 mg
$ 2000.00

American Custom Chemicals Corporation
TRIMETHYL (2-N-T-BUTOXYCARBONYLAMINO)ETHYLAMMONIUM BROMIDE 95.00%
500MG
$ 1732.50

American Custom Chemicals Corporation
TRIMETHYL (2-N-T-BUTOXYCARBONYLAMINO)ETHYLAMMONIUM BROMIDE 95.00%
50MG
$ 292.95

Total 1 raw suppliers

Chemical Property of TRIMETHYL (2-N-T-BUTOXYCARBONYLAMINO)ETHYLAMMONIUM BROMIDE

Chemical Property:

Melting Point:138-141°C
Storage Temp.:Hygroscopic, -20°C Freezer, Under inert atmosphere
Solubility.:Methanol (Slightly), Water (Slightly)

Purity/Quality:

99% ^*data from raw suppliers

Trimethyl(2-N-t-Butoxycarbonylamino)ethylammoniumBromide ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Uses Trimethyl (2-N-t-Butoxycarbonylamino)ethylammonium Bromide is a compound useful in organic synthesis.

Technology Process of TRIMETHYL (2-N-T-BUTOXYCARBONYLAMINO)ETHYLAMMONIUM BROMIDE

There total 3 articles about TRIMETHYL (2-N-T-BUTOXYCARBONYLAMINO)ETHYLAMMONIUM BROMIDE 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: 80.0%

: 57260-73-8
N-BOC-1,2-diaminoethane

: 74-88-4
methyl iodide

: 945713-45-1
2-((tert-butoxycarbonyl)amino)-N,N,N-trimethylethan-1-aminium

Guidance literature:: N-BOC-1,2-diaminoethane; With potassium carbonate; In acetonitrile; at 60 ℃; for 0.5h;

methyl iodide; In acetonitrile; for 20h; Reflux;
DOI:10.1039/c6cc04089f

Reference yield:

: 196200-04-1
tert-butyl (2-(dimethylamino)ethyl)carbamate

: 74-88-4
methyl iodide

: 945713-45-1
2-((tert-butoxycarbonyl)amino)-N,N,N-trimethylethan-1-aminium

Guidance literature:: With sodium hydroxide; In water; acetonitrile; at 65 ℃; for 3h;

Reference yield:

: 24424-99-5
di-tert-butyl dicarbonate

: 945713-45-1
2-((tert-butoxycarbonyl)amino)-N,N,N-trimethylethan-1-aminium

Guidance literature:: Multi-step reaction with 2 steps

1: sodium hydroxide / water; tetrahydrofuran / 2.33 h / 0 - 20 °C

2: sodium hydroxide / water; acetonitrile / 3 h / 65 °C

With sodium hydroxide; In tetrahydrofuran; water; acetonitrile;