Acetic acid, (p-((3-methyl-5-oxo-2-pyrazolin-4-ylidene)methyl)phenoxy)-, (4-amino-alpha-methylbenzylidene)hydrazide

Base Information

Chemical Name:Acetic acid, (p-((3-methyl-5-oxo-2-pyrazolin-4-ylidene)methyl)phenoxy)-, (4-amino-alpha-methylbenzylidene)hydrazide
CAS No.:107045-04-5
Molecular Formula:C₂₁H₂₁N₅O₃
Molecular Weight:391.429
Hs Code.:

Synonyms:BRN 5643941;Acetic acid, (p-((3-methyl-5-oxo-2-pyrazolin-4-ylidene)methyl)phenoxy)-, (4-amino-alpha-methylbenzylidene)hydrazide;107045-04-5;C21H21N5O3

Suppliers and Price of Acetic acid, (p-((3-methyl-5-oxo-2-pyrazolin-4-ylidene)methyl)phenoxy)-, (4-amino-alpha-methylbenzylidene)hydrazide

Supply Marketing:

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

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Chemical Property of Acetic acid, (p-((3-methyl-5-oxo-2-pyrazolin-4-ylidene)methyl)phenoxy)-, (4-amino-alpha-methylbenzylidene)hydrazide

Chemical Property:

XLogP3:2.1
Hydrogen Bond Donor Count:3
Hydrogen Bond Acceptor Count:6
Rotatable Bond Count:6
Exact Mass:391.16443955
Heavy Atom Count:29
Complexity:699

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CC1=NNC(=O)C1=CC2=CC=C(C=C2)OCC(=O)NN=C(C)C3=CC=C(C=C3)N
Isomeric SMILES:CC\1=NNC(=O)/C1=C\C2=CC=C(C=C2)OCC(=O)N/N=C(\C)/C3=CC=C(C=C3)N

Technology Process of Acetic acid, (p-((3-methyl-5-oxo-2-pyrazolin-4-ylidene)methyl)phenoxy)-, (4-amino-alpha-methylbenzylidene)hydrazide

There total 4 articles about Acetic acid, (p-((3-methyl-5-oxo-2-pyrazolin-4-ylidene)methyl)phenoxy)-, (4-amino-alpha-methylbenzylidene)hydrazide 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%

: 99-92-3
p-aminobenzophenone

: 107045-08-9
4-(3-Methyl-5-oxo-4-pyrazolidenemethyl)-phenoxyacetic acid hydrazide

: 107045-04-5
{4-[3-Methyl-5-oxo-1,5-dihydro-pyrazol-(4Z)-ylidenemethyl]-phenoxy}-acetic acid [1-(4-amino-phenyl)-eth-(E)-ylidene]-hydrazide

Guidance literature:: With acetic acid; In ethanol; for 3h; Heating;

Reference yield:

: 51264-69-8
ethyl 2-(4-formylphenoxy)acetate

: 107045-04-5
{4-[3-Methyl-5-oxo-1,5-dihydro-pyrazol-(4Z)-ylidenemethyl]-phenoxy}-acetic acid [1-(4-amino-phenyl)-eth-(E)-ylidene]-hydrazide

Guidance literature:: Multi-step reaction with 3 steps

1: 95 percent / piperidine / ethanol / 4 h / Heating

2: 70 percent / hydrazine hydrate / ethanol / 4 h / Heating

3: 50 percent / gl. acetic acid / ethanol / 3 h / Heating

With piperidine; hydrazine hydrate; acetic acid; In ethanol;

Reference yield:

: 123-08-0,65581-83-1
4-hydroxy-benzaldehyde

: 107045-04-5
{4-[3-Methyl-5-oxo-1,5-dihydro-pyrazol-(4Z)-ylidenemethyl]-phenoxy}-acetic acid [1-(4-amino-phenyl)-eth-(E)-ylidene]-hydrazide

Guidance literature:: Multi-step reaction with 4 steps

1: K₂CO₃ / acetone / 10 h / Heating

2: 95 percent / piperidine / ethanol / 4 h / Heating

3: 70 percent / hydrazine hydrate / ethanol / 4 h / Heating

4: 50 percent / gl. acetic acid / ethanol / 3 h / Heating

With piperidine; potassium carbonate; hydrazine hydrate; acetic acid; In ethanol; acetone;