2-Phenyltetrazole-5-carbonitrile

Base Information

Chemical Name:2-Phenyltetrazole-5-carbonitrile
CAS No.:78984-92-6
Molecular Formula:C₈H₅N₅
Molecular Weight:171.161
Hs Code.:
NSC Number:141850
DSSTox Substance ID:DTXSID90301215
Nikkaji Number:J361.113B
Wikidata:Q82044890

Synonyms:78984-92-6;2-phenyltetrazole-5-carbonitrile;2-phenyl-2h-tetrazole-5-carbonitrile;NSC141850;2-phenyl-5-cyanotetrazole;SCHEMBL4407197;DTXSID90301215;NSC-141850

Suppliers and Price of 2-Phenyltetrazole-5-carbonitrile

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 6 raw suppliers

Chemical Property of 2-Phenyltetrazole-5-carbonitrile

Chemical Property:

Vapor Pressure:3.73E-05mmHg at 25°C
Boiling Point:352.9°C at 760 mmHg
Flash Point:167.2°C
Density:1.35g/cm³
XLogP3:1.8
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:4
Rotatable Bond Count:1
Exact Mass:171.05449518
Heavy Atom Count:13
Complexity:214

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

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Canonical SMILES:C1=CC=C(C=C1)N2N=C(N=N2)C#N

Technology Process of 2-Phenyltetrazole-5-carbonitrile

There total 4 articles about 2-Phenyltetrazole-5-carbonitrile 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:

: 121564-84-9
1-amino-5-phenyl-1,5-dihydro<1,2,3>triazolo<4,5-d><1,2,3>-triazole

: 78984-92-6
2-phenyl-2H-tetrazole-5-carbonitrile

Guidance literature:: Multi-step reaction with 2 steps

1: 81 percent / lead tetraacetate / CH₂Cl₂ / 0 °C

2: CH₂Cl₂ / Ambient temperature

With lead(IV) acetate; In dichloromethane;
DOI:10.1039/c39880001608

Reference yield:

: 136649-99-5
5-phenyl-1,5-dihydro-[1,2,3]triazolo[4,5-d][1,2,3]triazole

: 78984-92-6
2-phenyl-2H-tetrazole-5-carbonitrile

Guidance literature:: Multi-step reaction with 3 steps

1: 22 percent / O-(mesitylsulphonyl)hydroxylamine (MSH), NaH / tetrahydrofuran; benzene / 0.25 h / 0 °C

2: 81 percent / 90percent Pb(OAc)4 (LTA) / CH₂Cl₂ / 0.25 h / 0 °C / other <1,2,3>triazolo<4,5-d><1,2,3>triazole derivative

3: CH₂Cl₂ / 2 h / Ambient temperature; other solvents

With lead(IV) acetate; mesitylenesulfonylhydroxylamine; sodium hydride; In tetrahydrofuran; dichloromethane; benzene;