N-Ethylnordiazepam

Base Information

Chemical Name:N-Ethylnordiazepam
CAS No.:5571-65-3
Molecular Formula:C17H15 Cl N2 O
Molecular Weight:298.772
Hs Code.:
Mol file:5571-65-3.mol

Synonyms:7-Chloro-1-ethyl-5-phenyl-1,3-dihydrobenzo[e][1,4]diazepin-2-one;N-Ethylnordiazepam

Suppliers and Price of N-Ethylnordiazepam

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

Biosynth Carbosynth
N-Desmethyl-N-ethyl diazepam
50 mg
$ 1638.00

Biosynth Carbosynth
N-Desmethyl-N-ethyl diazepam
25 mg
$ 901.00

Biosynth Carbosynth
N-Desmethyl-N-ethyl diazepam
10 mg
$ 495.50

Biosynth Carbosynth
N-Desmethyl-N-ethyl diazepam
5 mg
$ 272.60

Biosynth Carbosynth
N-Desmethyl-N-ethyl diazepam
2 mg
$ 149.90

Total 3 raw suppliers

Chemical Property of N-Ethylnordiazepam

Chemical Property:

Boiling Point:°Cat760mmHg
Flash Point:°C
Density:1.37g/cm³

Purity/Quality:

97% ^*data from raw suppliers

N-Desmethyl-N-ethyl diazepam ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Uses A metabolite of Diazepam (D416855).

Technology Process of N-Ethylnordiazepam

There total 1 articles about N-Ethylnordiazepam 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:

: 74-96-4
ethyl bromide

: 1088-11-5
desmethyldiazepam

: 5571-65-3
7-chloro-5-phenyl-1,3-dihydro-1-ethyl-2H-1,4-benzodiazepin-2-one

Guidance literature:: With sodium hydride; Yield given. Multistep reaction; 1.) DMF, 0 deg C, 15 min, 2.) DMF, RT, 48 h;
DOI:10.1002/jhet.5570300416