3H-Pyrazol-3-one, 2-benzoyl-2,4-dihydro-5-methyl-

Base Information

Chemical Name:3H-Pyrazol-3-one, 2-benzoyl-2,4-dihydro-5-methyl-
CAS No.:51686-30-7
Molecular Formula:C₁₁H₁₀N₂O₂
Molecular Weight:202.213
Hs Code.:
DSSTox Substance ID:DTXSID30407846
Wikidata:Q82213191
Mol file:51686-30-7.mol

Synonyms:51686-30-7;1-benzoyl-3-methyl-1H-pyrazol-5(4H)-one;3H-Pyrazol-3-one, 2-benzoyl-2,4-dihydro-5-methyl-;DTXSID30407846

Suppliers and Price of 3H-Pyrazol-3-one, 2-benzoyl-2,4-dihydro-5-methyl-

Supply Marketing:

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 3H-Pyrazol-3-one, 2-benzoyl-2,4-dihydro-5-methyl-

Chemical Property:

XLogP3:1.2
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:3
Rotatable Bond Count:1
Exact Mass:202.074227566
Heavy Atom Count:15
Complexity:317

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CC1=NN(C(=O)C1)C(=O)C2=CC=CC=C2

Technology Process of 3H-Pyrazol-3-one, 2-benzoyl-2,4-dihydro-5-methyl-

There total 2 articles about 3H-Pyrazol-3-one, 2-benzoyl-2,4-dihydro-5-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:

: 163352-70-3
3-(Benzoyl-hydrazono)-butyric acid ethyl ester

: 51686-30-7
1-Benzoyl-3-Methyl-1H-Pyrazol-5(4H)-One

Guidance literature:: In 1,2-dichloro-benzene; for 5h; Heating;

Reference yield:

: 613-94-5
benzoic acid hydrazide

: 51686-30-7
1-Benzoyl-3-Methyl-1H-Pyrazol-5(4H)-One

Guidance literature:: Multi-step reaction with 2 steps

1: dioxane / 4 h / Heating

2: 1,2-dichloro-benzene / 5 h / Heating

In 1,4-dioxane; 1,2-dichloro-benzene;