Fenamole

Base Information

Chemical Name:Fenamole
CAS No.:5467-78-7
Molecular Formula:C7H7 N5
Molecular Weight:161.166
Hs Code.:
European Community (EC) Number:226-780-4
NSC Number:25413
UNII:K4H264PBQ7
DSSTox Substance ID:DTXSID4048694
Nikkaji Number:J7.985E
Wikidata:Q27281951
NCI Thesaurus Code:C80547
Metabolomics Workbench ID:153482
ChEMBL ID:CHEMBL2106224
Mol file:5467-78-7.mol

Synonyms:FENAMOLE;5467-78-7;Fenamol;1H-Tetrazol-5-amine, 1-phenyl-;5-Amino-1-phenyltetrazole;1-phenyl-1H-tetrazol-5-amine;1-Phenyl-5-aminotetrazole;5-Amino-1-phenyl-1H-tetrazole;AL 0559;1-phenyl-1H-1,2,3,4-tetrazol-5-amine;Fenamolum;PAT;Fenamol [INN-Spanish];Fenamole [USAN:INN];Fenamolum [INN-Latin];P-463;1H-Tetrazole, 5-amino-1-phenyl-;NSC-25413;UNII-K4H264PBQ7;BM 2;K4H264PBQ7;DTXSID4048694;Fenamole (USAN);NSC25413;EINECS 226-780-4;AL0559;NSC 25413;AL-0559;NCGC00160436-01;FENAMOLE [USAN];1-phenyltetrazol-5-amine;DTXCID4028620;CAS-5467-78-7;FENAMOLE [INN];SCHEMBL43680;1-phenyl-2H-tetrazol-5-imine;1-phenyl-5-amino-1H-tetrazole;CHEMBL2106224;Tox21_113085;BBL034719;MFCD00083048;STL412408;AKOS000111560;Tox21_113085_1;DB12506;NCGC00160436-02;1-Phenyl-1,2-dihydro-5H-tetraazol-5-imine;CS-0081823;P 463;EN300-66080;1B-050;D04139;SR-01000945151;SR-01000945151-1;BRD-K12179389-001-01-2;Q27281951;Z56788744

Suppliers and Price of Fenamole

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 37 raw suppliers

Chemical Property of Fenamole

Chemical Property:

Vapor Pressure:1.17E-05mmHg at 25°C
Refractive Index:1.7000 (estimate)
Boiling Point:369.7°Cat760mmHg
Flash Point:177.4°C
PSA：69.62000
Density:1.46g/cm³
LogP:0.82570
XLogP3:0.2
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:4
Rotatable Bond Count:1
Exact Mass:161.07014524
Heavy Atom Count:12
Complexity:145

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)N2C(=NN=N2)N
Recent ClinicalTrials:Clinical Effects of Two New Chlorhexidine Digluconate Formulations: 0.12% and 0.03%.
Uses Anti-inflammatory.

Technology Process of Fenamole

There total 25 articles about Fenamole 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: 96.0%

: 4418-61-5
5-aminotetrazole

: 591-50-4
iodobenzene

: 5467-78-7
fenamole

Guidance literature:: With 1,10-Phenanthroline; copper(II) acetate monohydrate; caesium carbonate; In dimethyl sulfoxide; at 85 ℃; for 18h; regioselective reaction;
DOI:10.1016/j.jorganchem.2018.04.027

Reference yield: 95.0%

: 1197040-29-1,931-54-4
phenyl isocyanate

: 5467-78-7
fenamole

Guidance literature:: With trimethylsilylazide; [Au(MeCN)(PPh₃)][SbF₆]; In methanol; dichloromethane; at 20 ℃; for 3h; Schlenk technique; Inert atmosphere;
DOI:10.1002/chem.201803252

Reference yield: 92.0%

: 103-85-5
monophenylthiourea

: 5467-78-7
fenamole

Guidance literature:: monophenylthiourea; With iron(III) sulphate monohydrate; triethylamine; In dimethyl sulfoxide; at 20 ℃; for 2h;

With sodium azide; In dimethyl sulfoxide; at 20 ℃; for 3h; Reagent/catalyst; Solvent; regioselective reaction; Catalytic behavior;
DOI:10.1080/17415993.2021.1909589