Benzamide, N-(2-aminoethyl)-4-azido-

Base Information

Chemical Name:Benzamide, N-(2-aminoethyl)-4-azido-
CAS No.:81416-99-1
Molecular Formula:C₉H₁₁N₅O
Molecular Weight:205.219
Hs Code.:
DSSTox Substance ID:DTXSID60231090
Wikidata:Q83111906

Synonyms:Benzamide, N-(2-aminoethyl)-4-azido-;N-(2-Aminoethyl)-4-azidobenzamide;81416-99-1;aminoethyl p-azidobenzamide;DTXSID60231090

Suppliers and Price of Benzamide, N-(2-aminoethyl)-4-azido-

Supply Marketing:

Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

Manufacturers and distributors:

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Chemical Property of Benzamide, N-(2-aminoethyl)-4-azido-

Chemical Property:

Boiling Point:°Cat760mmHg
Flash Point:°C
Density:g/cm³
XLogP3:1
Hydrogen Bond Donor Count:2
Hydrogen Bond Acceptor Count:4
Rotatable Bond Count:4
Exact Mass:205.09635999
Heavy Atom Count:15
Complexity:253

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:C1=CC(=CC=C1C(=O)NCCN)N=[N+]=[N-]

Technology Process of Benzamide, N-(2-aminoethyl)-4-azido-

There total 4 articles about Benzamide, N-(2-aminoethyl)-4-azido- 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: 59.0%

: 53053-08-0
4-azidobenzoic acid N-hydroxysuccinimide ester

: 107-15-3,85404-18-8
ethylenediamine

: 81416-99-1
N-(4-azido-benzoyl)-1,2-ethanediamine

Guidance literature:: In methanol; dichloromethane;
DOI:10.1021/jm200692n

Reference yield:

: tert-butyl (2-(4-azidobenzamido)ethyl)carbamate

: 81416-99-1
N-(4-azido-benzoyl)-1,2-ethanediamine

Guidance literature:: With trifluoroacetic acid; In chloroform; at 20 - 22 ℃; Inert atmosphere;
DOI:10.1002/open.201500059

Reference yield:

: 6427-66-3
4-azidobenzoic acid

: 81416-99-1
N-(4-azido-benzoyl)-1,2-ethanediamine

Guidance literature:: Multi-step reaction with 2 steps

1: dicyclohexyl-carbodiimide / tetrahydrofuran / Inert atmosphere

2: methanol; dichloromethane

With dicyclohexyl-carbodiimide; In tetrahydrofuran; methanol; dichloromethane;
DOI:10.1021/jm200692n