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[13C]-9-Methylfluorene-9-carbonyl chloride

Base Information
  • Chemical Name:[13C]-9-Methylfluorene-9-carbonyl chloride
  • CAS No.:1072315-89-9
  • Molecular Formula:C15H11ClO
  • Molecular Weight:243.70924
  • Hs Code.:
  • Mol file:1072315-89-9.mol
[13C]-9-Methylfluorene-9-carbonyl chloride

Synonyms:[13C]-9-Methylfluorene-9-carbonyl chloride;13COgen;9-Methyl-9H-fluorene-9-carbonyl-13C chloride

Suppliers and Price of [13C]-9-Methylfluorene-9-carbonyl chloride
Supply Marketing:
Business phase:
The product has achieved commercial mass production*data from LookChem market partment
Manufacturers and distributors:
  • Manufacture/Brand
  • Chemicals and raw materials
  • Packaging
  • price
  • Sigma-Aldrich
  • 9-Methyl-9H-fluorene-9-carbonyl-13C chloride ≥97.0% (GC)
  • 1g
  • $ 1090.00
  • Sigma-Aldrich
  • 9-Methyl-9H-fluorene-9-carbonyl-13C chloride ≥97.0% (GC)
  • 250mg
  • $ 328.00
Total 6 raw suppliers
Chemical Property of [13C]-9-Methylfluorene-9-carbonyl chloride
Chemical Property:
  • Flash Point:>110℃ 
  • PSA:17.07000 
  • LogP:3.73840 
Purity/Quality:

98%min *data from raw suppliers

9-Methyl-9H-fluorene-9-carbonyl-13C chloride ≥97.0% (GC) *data from reagent suppliers

Safty Information:
  • Pictogram(s):  
  • Hazard Codes:
  • Statements: 34 
  • Safety Statements: 26-36/37/39-45 
MSDS Files:

SDS file from LookChem

Useful:
  • Uses COGen is a simple alternative for carbon monoxide generation in the application of palladium-catalyzed carbonylation reactions. This reagent has proved to be applicable in a wide range of applications and is compatible with several building blocks in the formation of ketones, amides, esters, etc.For more information please visit: Technology Spotlight, Professor Skrystrup PPP
Technology Process of [13C]-9-Methylfluorene-9-carbonyl chloride

There total 5 articles about [13C]-9-Methylfluorene-9-carbonyl chloride 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:
Multi-step reaction with 5 steps
2.1: acetic acid / Reflux
3.1: palladium on carbon; hydrogen / 760.05 Torr
4.1: n-butyllithium / tetrahydrofuran; hexane / -78 °C / Inert atmosphere
4.2: -78 - 20 °C
5.1: oxalyl dichloride; N,N-dimethyl-formamide / dichloromethane / 3 h / 30 °C / Inert atmosphere
With n-butyllithium; oxalyl dichloride; palladium on carbon; hydrogen; acetic acid; N,N-dimethyl-formamide; In tetrahydrofuran; hexane; dichloromethane;
DOI:10.1021/ja200818w
Guidance literature:
Multi-step reaction with 4 steps
1.1: acetic acid / Reflux
2.1: palladium on carbon; hydrogen / 760.05 Torr
3.1: n-butyllithium / tetrahydrofuran; hexane / -78 °C / Inert atmosphere
3.2: -78 - 20 °C
4.1: oxalyl dichloride; N,N-dimethyl-formamide / dichloromethane / 3 h / 30 °C / Inert atmosphere
With n-butyllithium; oxalyl dichloride; palladium on carbon; hydrogen; acetic acid; N,N-dimethyl-formamide; In tetrahydrofuran; hexane; dichloromethane;
DOI:10.1021/ja200818w
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