Propaneperoxoic acid, 2,2-dimethyl-

Base Information

• Chemical Name: Propaneperoxoic acid, 2,2-dimethyl-
• CAS No.: 14909-78-5
• Molecular Formula: C5H10O3
• Molecular Weight: 118.133
• DSSTox Substance ID: DTXSID70431009
• Nikkaji Number: J810.372K
• Wikidata: Q82244777
• Mol file: 14909-78-5.mol

Synonyms:Propaneperoxoic acid, 2,2-dimethyl-;14909-78-5;SCHEMBL1309625;2,2-Dimethylperoxypropionic acid;DTXSID70431009

Chemical Property of Propaneperoxoic acid, 2,2-dimethyl-

Chemical Property:

• XLogP3: 1
• Hydrogen Bond Donor Count: 1
• Hydrogen Bond Acceptor Count: 3
• Rotatable Bond Count: 2
• Exact Mass: 118.062994177
• Heavy Atom Count: 8
• Complexity: 90.3

Purity/Quality:

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: CC(C)(C)C(=O)OO

Technology Process of Propaneperoxoic acid, 2,2-dimethyl-

There total 1 articles about Propaneperoxoic acid, 2,2-dimethyl- 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:

4-nitrophenyl pivalate (4195-17-9) → tert-butyl hydroperoxide (14909-78-5) + p-nitrophenolate (14609-74-6)

Guidance literature:

With triblock copolymer E₂₇P₆₁E₂₇; dihydrogen peroxide; sodium hydrogencarbonate; sodium carbonate; In various solvent(s); at 25 ℃; pH=9.5; Further Variations:; Reagents; Temperatures; Kinetics; Thermodynamic data;

DOI:10.1039/b210239k

Reference yield:

tert-butyl hydroperoxide (14909-78-5) → Trimethylacetic acid (75-98-9)

Guidance literature:

With Dequest 2060; anthracene-9,10-bis(ethanesulphonate) caesium salt; In various solvent(s); at 25 ℃; Rate constant; different chelating agents;

upstream raw materials:

4-nitrophenyl pivalate

Downstream raw materials:

Trimethylacetic acid

Refernces