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Propanoic acid, 2,2-dimethyl-, 4-(bromomethyl)phenyl ester

Base Information Edit
  • Chemical Name:Propanoic acid, 2,2-dimethyl-, 4-(bromomethyl)phenyl ester
  • CAS No.:58305-26-3
  • Molecular Formula:C12H15BrO2
  • Molecular Weight:271.154
  • Hs Code.:
  • DSSTox Substance ID:DTXSID20467535
  • Nikkaji Number:J2.257.965G
  • Wikidata:Q82294514
  • Mol file:58305-26-3.mol
Propanoic acid, 2,2-dimethyl-, 4-(bromomethyl)phenyl ester

Synonyms:58305-26-3;4-(bromomethyl)phenyl pivalate;Propanoic acid, 2,2-dimethyl-, 4-(bromomethyl)phenyl ester;SCHEMBL7276499;DTXSID20467535

Suppliers and Price of Propanoic acid, 2,2-dimethyl-, 4-(bromomethyl)phenyl ester
Supply Marketing:Edit
Business phase:
The product has achieved commercial mass production*data from LookChem market partment
Manufacturers and distributors:
  • Manufacture/Brand
  • Chemicals and raw materials
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Total 0 raw suppliers
Chemical Property of Propanoic acid, 2,2-dimethyl-, 4-(bromomethyl)phenyl ester Edit
Chemical Property:
  • XLogP3:3.6
  • Hydrogen Bond Donor Count:0
  • Hydrogen Bond Acceptor Count:2
  • Rotatable Bond Count:4
  • Exact Mass:270.02554
  • Heavy Atom Count:15
  • Complexity:212
Purity/Quality:
Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:

SDS file from LookChem

Useful:
  • Canonical SMILES:CC(C)(C)C(=O)OC1=CC=C(C=C1)CBr
Technology Process of Propanoic acid, 2,2-dimethyl-, 4-(bromomethyl)phenyl ester

There total 4 articles about Propanoic acid, 2,2-dimethyl-, 4-(bromomethyl)phenyl ester 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:
Guidance literature:
With methanesulfonyl chloride; triethylamine; lithium bromide; In tetrahydrofuran; at 0 ℃; for 2h;
DOI:10.1021/jo051568z
Guidance literature:
Multi-step reaction with 2 steps
1: KOH / dioxane
2: NBS; TPP / CH2Cl2
With potassium hydroxide; N-Bromosuccinimide; thiamine diphosphate; In 1,4-dioxane; dichloromethane; 1: Schotten-Baumann pivaloylation;
DOI:10.1021/np049796w
Guidance literature:
Multi-step reaction with 2 steps
1: 80 percent / sodium hydride / tetrahydrofuran / 2.5 h / 0 - 20 °C
2: 81 percent / lithium bromide; methanesulfonyl chloride; triethylamine / tetrahydrofuran / 2 h / 0 °C
With sodium hydride; methanesulfonyl chloride; triethylamine; lithium bromide; In tetrahydrofuran;
DOI:10.1021/jo061395t
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