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Technology Process of 3,5,5-trimethyl-2-oxido-4,5-dihydro-3H-pyrazol-3-yl benzoate

3,5,5-trimethyl-2-oxido-4,5-dihydro-3H-pyrazol-3-yl benzoate

Base Information
  • Chemical Name:3,5,5-trimethyl-2-oxido-4,5-dihydro-3H-pyrazol-3-yl benzoate
  • CAS No.:65441-91-0
  • Molecular Formula:C13H16N2O3
  • Molecular Weight:248.2777
  • Hs Code.:
3,5,5-trimethyl-2-oxido-4,5-dihydro-3H-pyrazol-3-yl benzoate

Synonyms:

Suppliers and Price of 3,5,5-trimethyl-2-oxido-4,5-dihydro-3H-pyrazol-3-yl benzoate
Supply Marketing:
Business phase:
The product has achieved commercial mass production*data from LookChem market partment
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Chemical Property of 3,5,5-trimethyl-2-oxido-4,5-dihydro-3H-pyrazol-3-yl benzoate
Chemical Property:
  • Vapor Pressure:4.22E-05mmHg at 25°C 
  • Boiling Point:351°Cat760mmHg 
  • Flash Point:166.1°C 
  • Density:1.18g/cm3 
Purity/Quality:

99% *data from raw suppliers

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MSDS Files:

SDS file from LookChem

Useful:
Technology Process of 3,5,5-trimethyl-2-oxido-4,5-dihydro-3H-pyrazol-3-yl benzoate

There total 1 articles about 3,5,5-trimethyl-2-oxido-4,5-dihydro-3H-pyrazol-3-yl benzoate 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:

3-benzoyloxy-3,5,5-trimethyl-4,5-dihydro-3<i>H</i>-pyrazole 2-oxide
65441-91-0

3-benzoyloxy-3,5,5-trimethyl-4,5-dihydro-3H-pyrazole 2-oxide

Guidance literature:
DOI:10.1016/S0040-4039(01)99260-3
Refernces

10.1016/0040-4039(81)80111-6

The study focuses on determining the absolute configuration of the K-region 4,5-dihydrodiols and the 4,5-oxide derivatives of Benzo[a]pyrene (B[a]P). It discusses the methods used to resolve the stereoisomers and the biological implications of these configurations, particularly in the context of carcinogenesis.

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