1-(2-aminoethyl)-2,3-dihydro-1H-1,3-benzodiazol-2-one hydrochloride

Base Information

Chemical Name:1-(2-aminoethyl)-2,3-dihydro-1H-1,3-benzodiazol-2-one hydrochloride
CAS No.:64928-55-8
Molecular Formula:C9H11N3O.ClH
Molecular Weight:
Hs Code.:
European Community (EC) Number:848-341-1

Synonyms:1-(2-aminoethyl)-2,3-dihydro-1H-1,3-benzodiazol-2-one hydrochloride;64928-55-8;3-(2-aminoethyl)-1H-benzimidazol-2-one;hydrochloride;1-(2-aminoethyl)-1H-benzo[d]imidazol-2(3H)-one hydrochloride;1-(2-aminoethyl)-1,3-dihydro-2H-benzimidazol-2-one hydrochloride;SCHEMBL2985946;VFQPYJTVVDTJSI-UHFFFAOYSA-N;MFCD18459181;AKOS015958920;BS-17359;DB-190247;CS-0161969;D80807;EN300-101204;Z1354416053;1-(2-Aminoethyl)-2,3-dihydro-1H-1,3-benzodiazol-2-one HCl;1-(2-aminoethyl)-1h-benzo[d]imidazol-2(3h)-one hydrochloride salt;1-(2-AMINOETHYL)-3H-1,3-BENZODIAZOL-2-ONE HYDROCHLORIDE;1-(2-aminoethyl)-2,3-dihydro-1H-1,3-benzodiazol-2-onehydrochloride

Suppliers and Price of 1-(2-aminoethyl)-2,3-dihydro-1H-1,3-benzodiazol-2-one 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

Total 6 raw suppliers

Chemical Property of 1-(2-aminoethyl)-2,3-dihydro-1H-1,3-benzodiazol-2-one hydrochloride

Chemical Property:

Hydrogen Bond Donor Count:3
Hydrogen Bond Acceptor Count:2
Rotatable Bond Count:2
Exact Mass:213.0668897
Heavy Atom Count:14
Complexity:207

Purity/Quality:: 97% ^*data from raw suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Canonical SMILES:C1=CC=C2C(=C1)NC(=O)N2CCN.Cl

Technology Process of 1-(2-aminoethyl)-2,3-dihydro-1H-1,3-benzodiazol-2-one hydrochloride

There total 5 articles about 1-(2-aminoethyl)-2,3-dihydro-1H-1,3-benzodiazol-2-one 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: 100.0%

: 834881-65-1
tert-butyl (2-(2-oxo-2,3-dihydro-1H-benzo[d]imidazol-1-yl)ethyl)carbamate

: 64928-55-8
3-(2-aminoethyl)-1H-benzimidazol-2-one hydrochloride

Guidance literature:: With hydrogenchloride; In diethyl ether; at 20 ℃; for 5h;

Reference yield:

: 834881-63-9
tert‐butyl (3‐((2‐nitrophenyl)amino)ethyl)carbamate

: 64928-55-8
3-(2-aminoethyl)-1H-benzimidazol-2-one hydrochloride

Guidance literature:: Multi-step reaction with 3 steps

1: palladium 10% on activated carbon; hydrogen / methanol / 18 h / 2 - 9 °C / 775.74 Torr / Inert atmosphere

2: tetrahydrofuran / 2 h / 80 °C

3: hydrogenchloride / 1,4-dioxane; dichloromethane / 1 h / 0 - 12 °C

With hydrogenchloride; palladium 10% on activated carbon; hydrogen; In tetrahydrofuran; 1,4-dioxane; methanol; dichloromethane;

Reference yield:

: 834881-64-0
tert‐butyl (3‐((2‐aminophenyl)amino)ethyl)carbamate

: 64928-55-8
3-(2-aminoethyl)-1H-benzimidazol-2-one hydrochloride

Guidance literature:: Multi-step reaction with 2 steps

1: tetrahydrofuran / 2 h / 80 °C

2: hydrogenchloride / 1,4-dioxane; dichloromethane / 1 h / 0 - 12 °C

With hydrogenchloride; In tetrahydrofuran; 1,4-dioxane; dichloromethane;