7-Phenyl[1,2,4]triazolo[1,5-a]pyrimidine

Base Information

Chemical Name:7-Phenyl[1,2,4]triazolo[1,5-a]pyrimidine
CAS No.:39573-72-3
Molecular Formula:C11H8N4
Molecular Weight:196.211
Hs Code.:
DSSTox Substance ID:DTXSID30358501
Nikkaji Number:J3.268.705I
Wikidata:Q82139116
Mol file:39573-72-3.mol

Synonyms:7-phenyl-[1,2,4]triazolo[1,5-a]pyrimidine;39573-72-3;7-phenyl[1,2,4]triazolo[1,5-a]pyrimidine;SCHEMBL11476738;DTXSID30358501;NJZKWMXLDGCTGY-UHFFFAOYSA-N;MFCD00138766;AKOS003145938;7-Phenyl-1,2,4-triazolo[1,5-a]pyrimidine;CS-0271168;1D-133;7-phenyl-8H-[1,2,4]triazolo[1,5-a]pyrimidine;SR-00000002441;SR-00000002441-1

Suppliers and Price of 7-Phenyl[1,2,4]triazolo[1,5-a]pyrimidine

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
7-PHENYL[1,2,4]TRIAZOLO[1,5-A]PYRIMIDINE 95.00%
5MG
$ 633.99

American Custom Chemicals Corporation
7-PHENYL[1,2,4]TRIAZOLO[1,5-A]PYRIMIDINE 95.00%
10MG
$ 631.85

American Custom Chemicals Corporation
7-PHENYL[1,2,4]TRIAZOLO[1,5-A]PYRIMIDINE 95.00%
1MG
$ 597.89

Total 4 raw suppliers

Chemical Property of 7-Phenyl[1,2,4]triazolo[1,5-a]pyrimidine

Chemical Property:

PSA：43.08000
LogP:1.79130
XLogP3:1.8
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:3
Rotatable Bond Count:1
Exact Mass:196.074896272
Heavy Atom Count:15
Complexity:215

Purity/Quality:

99% ^*data from raw suppliers

7-PHENYL[1,2,4]TRIAZOLO[1,5-A]PYRIMIDINE 95.00% ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:C1=CC=C(C=C1)C2=CC=NC3=NC=NN23

Technology Process of 7-Phenyl[1,2,4]triazolo[1,5-a]pyrimidine

There total 15 articles about 7-Phenyl[1,2,4]triazolo[1,5-a]pyrimidine 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: 94.0%

: 1201-93-0
1-phenyl-3-dimethylaminoprop-2-enone

: 61-82-5
3-amino-1,2,4-triazole

: 39573-72-3
7-phenyl-1,2,4-triazolo<1,5-a>pyrimidine

Guidance literature:: In acetic acid; for 16h; Solvent; Temperature; Time; Reflux;
DOI:10.1016/j.ultsonch.2013.12.007

Reference yield: 88.0%

: 3-Chlor-3-phenyl-prop-2-en-1-yliden-dimethyliminium-perchlorat

: 61-82-5
3-amino-1,2,4-triazole

: 39573-72-3
7-phenyl-1,2,4-triazolo<1,5-a>pyrimidine

Guidance literature:: With sodium hydride; In N,N-dimethyl-formamide; room t., 1 h, reflux, 1 h;
DOI:10.1016/S0040-4020(01)89564-8

Reference yield: 86.0%

: 275-02-5
1-deaza-5-azapurine

: 591-50-4
iodobenzene

: 39573-72-3
7-phenyl-1,2,4-triazolo<1,5-a>pyrimidine

Guidance literature:: With potassium phosphate; copper(l) iodide; 1,10-Phenanthroline; Trimethylacetic acid; In 1,4-dioxane; at 140 ℃; for 24h; regioselective reaction; Inert atmosphere; Schlenk technique;
DOI:10.1021/jacs.6b03890