4-(1H-tetrazol-5-ylmethyl)phenol

Base Information

Chemical Name:4-(1H-tetrazol-5-ylmethyl)phenol
CAS No.:119192-12-0
Molecular Formula:C8H8 N4 O
Molecular Weight:176.178
Hs Code.:
DSSTox Substance ID:DTXSID30560369
Wikidata:Q82443488
Mol file:119192-12-0.mol

Synonyms:119192-12-0;4-(1H-tetrazol-5-ylmethyl)phenol;4-(2H-tetrazol-5-ylmethyl)phenol;Phenol, 4-(2H-tetrazol-5-ylmethyl)-;4-((1H-Tetrazol-5-yl)methyl)phenol;4-[(2H-1,2,3,4-TETRAZOL-5-YL)METHYL]PHENOL;4-[(2H-Tetrazol-5-yl)methyl]phenol;SCHEMBL13498106;SCHEMBL18496473;DTXSID30560369;MEEDVZNIMBGRPZ-UHFFFAOYSA-N;MFCD08669497;AKOS000297367;AKOS005528867;CS-0324829;4-(1H-tetrazol-5-ylmethyl)phenol, AldrichCPR;D78643;N,N-BIS(2-PHENYLETHYL)AMINEHYDROCHLORIDE;Phenol, 4-(1H-1,2,3,4-tetrazol-5-ylmethyl)-;4-[(1H-1,2,3,4-TETRAZOL-5-YL)METHYL]PHENOL

Suppliers and Price of 4-(1H-tetrazol-5-ylmethyl)phenol

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
4-(1H-TETRAZOL-5-YLMETHYL)PHENOL 95.00%
5MG
$ 496.13

Total 2 raw suppliers

Chemical Property of 4-(1H-tetrazol-5-ylmethyl)phenol

Chemical Property:

PSA：74.69000
LogP:0.49610
XLogP3:1.1
Hydrogen Bond Donor Count:2
Hydrogen Bond Acceptor Count:4
Rotatable Bond Count:2
Exact Mass:176.06981089
Heavy Atom Count:13
Complexity:158

Purity/Quality:

85.0-99.8% ^*data from raw suppliers

4-(1H-TETRAZOL-5-YLMETHYL)PHENOL 95.00% ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:C1=CC(=CC=C1CC2=NNN=N2)O

Technology Process of 4-(1H-tetrazol-5-ylmethyl)phenol

There total 3 articles about 4-(1H-tetrazol-5-ylmethyl)phenol 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: 98.0%

: 131117-50-5
5-(4-aminobenzyl)-tetrazole

: 119192-12-0
1-(p-hydroxybenzyl)-tetrazole

Guidance literature:: With sodium nitrate; sulfuric acid; In water; room temp., 20 min, 85 deg C, 35 min;

Reference yield:

: 18489-25-3
5-benzyl-2H-tetrazole

: 119192-12-0
1-(p-hydroxybenzyl)-tetrazole

Guidance literature:: Multi-step reaction with 3 steps

1: 33.5 percent / H₂SO₄-HNO₃ / 0.5 h / 10 °C

2: 98 percent / hydrogen / 5percent Pd/C / ethanol / Ambient temperature

3: 98 percent / H₂SO₄, NaNO₃ / H₂O / room temp., 20 min, 85 deg C, 35 min

With sodium nitrate; sulfuric acid; hydrogen; nitric acid; palladium on activated charcoal; In ethanol; water;

Reference yield:

: 131090-44-3
5-(p-nitrobenzyl)-tetrazole

: 119192-12-0
1-(p-hydroxybenzyl)-tetrazole

Guidance literature:: Multi-step reaction with 2 steps

1: 98 percent / hydrogen / 5percent Pd/C / ethanol / Ambient temperature

2: 98 percent / H₂SO₄, NaNO₃ / H₂O / room temp., 20 min, 85 deg C, 35 min

With sodium nitrate; sulfuric acid; hydrogen; palladium on activated charcoal; In ethanol; water;