1,2,4-Triazolo(3,4-a)phthalazine, 3-(4-methoxyphenyl)-6-((1-pyrrolidinyl)methyl)-

Base Information

Chemical Name:1,2,4-Triazolo(3,4-a)phthalazine, 3-(4-methoxyphenyl)-6-((1-pyrrolidinyl)methyl)-
CAS No.:98124-14-2
Molecular Formula:C₂₁H₂₁N₅O
Molecular Weight:359.431
Hs Code.:
DSSTox Substance ID:DTXSID50243465
Wikidata:Q83127559

Synonyms:98124-14-2;3-(4-Methoxyphenyl)-6-((1-pyrrolidinyl)methyl)-1,2,4-triazolo(3,4-a)phthalazine;1,2,4-Triazolo(3,4-a)phthalazine, 3-(4-methoxyphenyl)-6-((1-pyrrolidinyl)methyl)-;3-(4-methoxyphenyl)-6-(pyrrolidin-1-ylmethyl)-[1,2,4]triazolo[3,4-a]phthalazine;SCHEMBL10685547;C21H21N5O;DTXSID50243465;C21-H21-N5-O;LS-156605

Suppliers and Price of 1,2,4-Triazolo(3,4-a)phthalazine, 3-(4-methoxyphenyl)-6-((1-pyrrolidinyl)methyl)-

Supply Marketing:

Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

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Chemical Property of 1,2,4-Triazolo(3,4-a)phthalazine, 3-(4-methoxyphenyl)-6-((1-pyrrolidinyl)methyl)-

Chemical Property:

Boiling Point:°Cat760mmHg
Flash Point:°C
Density:1.33g/cm³
XLogP3:3
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:5
Rotatable Bond Count:4
Exact Mass:359.17461031
Heavy Atom Count:27
Complexity:491

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:COC1=CC=C(C=C1)C2=NN=C3N2N=C(C4=CC=CC=C43)CN5CCCC5

Technology Process of 1,2,4-Triazolo(3,4-a)phthalazine, 3-(4-methoxyphenyl)-6-((1-pyrrolidinyl)methyl)-

There total 9 articles about 1,2,4-Triazolo(3,4-a)phthalazine, 3-(4-methoxyphenyl)-6-((1-pyrrolidinyl)methyl)- 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: 50.0%

: 123-75-1
pyrrolidine

: 98124-12-0
6-chloromethyl-3-(4'methoxyphenyl)-1,2,4-triazolo<3,4-a>phthalazine

: 98124-14-2
3-(4'methoxyphenyl)-6-<(1-pyrrolidinyl)methyl>-1,2,4-triazolo<3,4-a>phthalazine

Guidance literature:: at 100 ℃; for 8h; steel bomb;

Reference yield:

: 19064-68-7
1-chloro-4-methylphthalazine

: 98124-14-2
3-(4'methoxyphenyl)-6-<(1-pyrrolidinyl)methyl>-1,2,4-triazolo<3,4-a>phthalazine

Guidance literature:: Multi-step reaction with 3 steps

1: 95 percent / 2-methoxy-ethanol / 14 h / Heating

2: 43 percent / N-bromosuccinimide / dibenzoyl peroxide / CCl₄ / 2 h / Heating; Irradiation

3: 8 h / 100 °C / steel bomb

With N-Bromosuccinimide; dibenzoyl peroxide; In tetrachloromethane; 2-methoxy-ethanol;

Reference yield:

: 3290-99-1
4-methoxybenzoic acid hydrazide

: 98124-14-2
3-(4'methoxyphenyl)-6-<(1-pyrrolidinyl)methyl>-1,2,4-triazolo<3,4-a>phthalazine

Guidance literature:: Multi-step reaction with 3 steps

1: 95 percent / 2-methoxy-ethanol / 14 h / Heating

2: 43 percent / N-bromosuccinimide / dibenzoyl peroxide / CCl₄ / 2 h / Heating; Irradiation

3: 8 h / 100 °C / steel bomb

With N-Bromosuccinimide; dibenzoyl peroxide; In tetrachloromethane; 2-methoxy-ethanol;