Benzeneacetyl azide

Base Information

Chemical Name:Benzeneacetyl azide
CAS No.:33054-04-5
Molecular Formula:C8H7N3O
Molecular Weight:161.163
Hs Code.:
DSSTox Substance ID:DTXSID00449137
Nikkaji Number:J623.182I
Wikidata:Q82268506

Synonyms:Benzeneacetyl azide;2-PHENYLACETYL AZIDE;phenylacetyl azide;33054-04-5;Phenylacetic acid azide;DTXSID00449137;AHA100695

Suppliers and Price of Benzeneacetyl azide

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 2 raw suppliers

Chemical Property of Benzeneacetyl azide

Chemical Property:

XLogP3:2.7
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:2
Rotatable Bond Count:2
Exact Mass:161.058911855
Heavy Atom Count:12
Complexity:202

Purity/Quality:: 99% ^*data from raw suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

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

Technology Process of Benzeneacetyl azide

There total 12 articles about Benzeneacetyl azide 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: 95.0%

: 122-78-1
phenylacetaldehyde

: 33054-04-5
phenylacetyl azide

Guidance literature:: With sodium azide; Dess-Martin periodane; In dichloromethane; at 0 ℃; for 1h;
DOI:10.1016/S0040-4039(03)00623-3

Reference yield: 87.0%

: 103-82-2
phenylacetic acid

: 33054-04-5
phenylacetyl azide

Guidance literature:: With sodium azide; trichloroacetonitrile; triphenylphosphine; In acetone; at 20 ℃; for 2h; Inert atmosphere;
DOI:10.1055/s-2008-1077979