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1,2,4-Triazolo(3,4-a)phthalazin-6-amine, N,N-bis(2-methoxyethyl)-3-(4-(1-methylethyloxy)phenyl)-

Base Information Edit
  • Chemical Name:1,2,4-Triazolo(3,4-a)phthalazin-6-amine, N,N-bis(2-methoxyethyl)-3-(4-(1-methylethyloxy)phenyl)-
  • CAS No.:113628-71-0
  • Molecular Formula:C24H29 N5 O3
  • Molecular Weight:435.5188
  • Hs Code.:
  • DSSTox Substance ID:DTXSID30150502
  • Wikidata:Q83016621
  • ChEMBL ID:CHEMBL430276
  • Mol file:113628-71-0.mol
1,2,4-Triazolo(3,4-a)phthalazin-6-amine, N,N-bis(2-methoxyethyl)-3-(4-(1-methylethyloxy)phenyl)-

Synonyms:BRN 6447412;1,2,4-Triazolo(3,4-a)phthalazin-6-amine, N,N-bis(2-methoxyethyl)-3-(4-(1-methylethyloxy)phenyl)-;N,N-Bis(2-methoxyethyl)-3-(4-isopropoxyphenyl)-1,2,4-triazolo(3,4-a)phthalazin-6-amine;113628-71-0;CHEMBL430276;DTXSID30150502;LS-156551

Suppliers and Price of 1,2,4-Triazolo(3,4-a)phthalazin-6-amine, N,N-bis(2-methoxyethyl)-3-(4-(1-methylethyloxy)phenyl)-
Supply Marketing:Edit
Business phase:
The product has achieved commercial mass production*data from LookChem market partment
Manufacturers and distributors:
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Total 0 raw suppliers
Chemical Property of 1,2,4-Triazolo(3,4-a)phthalazin-6-amine, N,N-bis(2-methoxyethyl)-3-(4-(1-methylethyloxy)phenyl)- Edit
Chemical Property:
  • Boiling Point:°Cat760mmHg 
  • Flash Point:°C 
  • Density:1.22g/cm3 
  • XLogP3:3.6
  • Hydrogen Bond Donor Count:0
  • Hydrogen Bond Acceptor Count:7
  • Rotatable Bond Count:10
  • Exact Mass:435.22703980
  • Heavy Atom Count:32
  • Complexity:552
Purity/Quality:
Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:

SDS file from LookChem

Useful:
  • Canonical SMILES:CC(C)OC1=CC=C(C=C1)C2=NN=C3N2N=C(C4=CC=CC=C43)N(CCOC)CCOC
Technology Process of 1,2,4-Triazolo(3,4-a)phthalazin-6-amine, N,N-bis(2-methoxyethyl)-3-(4-(1-methylethyloxy)phenyl)-

There total 3 articles about 1,2,4-Triazolo(3,4-a)phthalazin-6-amine, N,N-bis(2-methoxyethyl)-3-(4-(1-methylethyloxy)phenyl)- 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:
Guidance literature:
Multi-step reaction with 2 steps
1: 70 percent / Et3N / dioxane / 5 h / Heating
2: 79 percent / KI, HCl / ethanol / 8 h / 100 °C
With hydrogenchloride; triethylamine; potassium iodide; In 1,4-dioxane; ethanol;
DOI:10.1021/jm00401a010
Guidance literature:
Multi-step reaction with 2 steps
1: 70 percent / Et3N / dioxane / 5 h / Heating
2: 79 percent / KI, HCl / ethanol / 8 h / 100 °C
With hydrogenchloride; triethylamine; potassium iodide; In 1,4-dioxane; ethanol;
DOI:10.1021/jm00401a010
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