Welcome to LookChem.com Sign In|Join Free
  • or

Encyclopedia

(3-Phenyl-prop-1-ynyl)-(2,4,6-tri-tert-butyl-phenyl)-phosphane

Base Information
  • Chemical Name:(3-Phenyl-prop-1-ynyl)-(2,4,6-tri-tert-butyl-phenyl)-phosphane
  • CAS No.:154670-40-3
  • Molecular Formula:C27H37P
  • Molecular Weight:392.565
  • Hs Code.:
(3-Phenyl-prop-1-ynyl)-(2,4,6-tri-tert-butyl-phenyl)-phosphane

Synonyms:

Suppliers and Price of (3-Phenyl-prop-1-ynyl)-(2,4,6-tri-tert-butyl-phenyl)-phosphane
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
Total 0 raw suppliers
Chemical Property of (3-Phenyl-prop-1-ynyl)-(2,4,6-tri-tert-butyl-phenyl)-phosphane
Chemical Property:
Purity/Quality:
Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:
Useful:
Technology Process of (3-Phenyl-prop-1-ynyl)-(2,4,6-tri-tert-butyl-phenyl)-phosphane

There total 1 articles about (3-Phenyl-prop-1-ynyl)-(2,4,6-tri-tert-butyl-phenyl)-phosphane 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 ethylmagnesium bromide; Yield given. Multistep reaction; 1.) THF, 3 h, room temp.; 2.) THF, 20 min, 0 deg C;
Guidance literature:
Multi-step reaction with 2 steps
1: 1.) 1.05M phenyllithium; 2.) 1,2-dibromoethane / 1.) THF, cyclohexane, ether, 30 min, room temp.; 2.) THF, cyclohexane, ether, -78 deg C to room temp. then 1 h, room temp.
2: N-bromosuccinimide / CCl4 / 0.42 h / Heating
With N-Bromosuccinimide; phenyllithium; ethylene dibromide; In tetrachloromethane;
Guidance literature:
Multi-step reaction with 2 steps
1: 1.) 1.05M phenyllithium; 2.) 1,2-dibromoethane / 1.) THF, cyclohexane, ether, 30 min, room temp.; 2.) THF, cyclohexane, ether, -78 deg C to room temp. then 1 h, room temp.
2: N-bromosuccinimide / CCl4 / 0.42 h / Heating
With N-Bromosuccinimide; phenyllithium; ethylene dibromide; In tetrachloromethane;
upstream raw materials:

propargyl benzene

(2,4,6-tri-tert-butyl)phenylmonochlorophosphane

Downstream raw materials:

C54H72P2

Post a RFQ

Enter 15 to 2000 letters.Word count: 0 letters

Attach files(File Format: Jpeg, Jpg, Gif, Png, PDF, PPT, Zip, Rar,Word or Excel Maximum File Size: 3MB)

1 Customer Service

What can I do for you?
Get Best Price

Get Best Price for 154670-40-3