n-Hexyl anthranilate

Base Information

Chemical Name:n-Hexyl anthranilate
CAS No.:18189-05-4
Molecular Formula:C13H19 N O2
Molecular Weight:221.299
Hs Code.:2922439000
European Community (EC) Number:242-075-4
NSC Number:406529
UNII:7JCD6XG3XY
DSSTox Substance ID:DTXSID4066335
Nikkaji Number:J110.733J
Wikidata:Q81992935
ChEMBL ID:CHEMBL1518766
Mol file:18189-05-4.mol

Synonyms:Hexyl 2-aminobenzoate;n-Hexyl anthranilate;Hexyl anthranilate;18189-05-4;Anthranilic acid, hexyl ester;Benzoic acid, 2-amino-, hexyl ester;n-Hexyl o-aminobenzoate;7JCD6XG3XY;MLS000105034;EINECS 242-075-4;NSC 406529;NSC-406529;SMR000054963;AI3-03468;hexyl 2-azanylbenzoate;UNII-7JCD6XG3XY;Anthanilic acid hexyl ester;cid_87500;SCHEMBL4258769;2-aminobenzoic acid hexyl ester;CHEMBL1518766;DTXSID4066335;BDBM67790;2-amino-benzoic acid hexyl ester;HMS2331N22;BBL028628;NSC406529;STL373366;AKOS010556879;VS-08881;SR-01000196557;SR-01000196557-1

Suppliers and Price of n-Hexyl anthranilate

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

American Custom Chemicals Corporation
HEXYL 2-AMINOBENZOATE 95.00%
5MG
$ 502.49

Total 6 raw suppliers

Chemical Property of n-Hexyl anthranilate

Chemical Property:

Vapor Pressure:0.000188mmHg at 25°C
Boiling Point:328.6°C at 760 mmHg
Flash Point:178.4°C
PSA：52.32000
Density:1.043g/cm³
LogP:3.58710
XLogP3:4.5
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:3
Rotatable Bond Count:7
Exact Mass:221.141578849
Heavy Atom Count:16
Complexity:206

Purity/Quality:

99% ^*data from raw suppliers

HEXYL 2-AMINOBENZOATE 95.00% ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CCCCCCOC(=O)C1=CC=CC=C1N

Technology Process of n-Hexyl anthranilate

There total 5 articles about n-Hexyl anthranilate 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%