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3'-(AMINOMETHYL)-BIPHENYL-3-CARBOXYLIC ACID TERT-BUTYL ESTER

Base Information Edit
  • Chemical Name:3'-(AMINOMETHYL)-BIPHENYL-3-CARBOXYLIC ACID TERT-BUTYL ESTER
  • CAS No.:180977-31-5
  • Molecular Formula:C18H21NO2
  • Molecular Weight:283.37
  • Hs Code.:
  • Mol file:180977-31-5.mol
3'-(AMINOMETHYL)-BIPHENYL-3-CARBOXYLIC ACID TERT-BUTYL ESTER

Synonyms:3'-Aminomethyl-biphenyl-3-carboxylic acid tert-butyl ester

Suppliers and Price of 3'-(AMINOMETHYL)-BIPHENYL-3-CARBOXYLIC ACID TERT-BUTYL 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
  • Packaging
  • price
  • Acrotein
  • 3'-tert-Butoxylcarbonyl-3-biphenylmethanamineHCl 97%
  • 0.1g
  • $ 137.50
Total 2 raw suppliers
Chemical Property of 3'-(AMINOMETHYL)-BIPHENYL-3-CARBOXYLIC ACID TERT-BUTYL ESTER Edit
Chemical Property:
Purity/Quality:

95%-98% *data from raw suppliers

3'-tert-Butoxylcarbonyl-3-biphenylmethanamineHCl 97% *data from reagent suppliers

Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:
Useful:
Technology Process of 3'-(AMINOMETHYL)-BIPHENYL-3-CARBOXYLIC ACID TERT-BUTYL ESTER

There total 11 articles about 3'-(AMINOMETHYL)-BIPHENYL-3-CARBOXYLIC ACID TERT-BUTYL 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 hydrogen; Pd-BaSO4; In methanol; under 760 Torr;
DOI:10.1021/jm950414g
Guidance literature:
Multi-step reaction with 4 steps
1: sodium carbonate / tetrakis(triphenylphosphine) palladium(0) / tetrahydrofuran / 18 h / 80 °C
2: triethylamine / dichloromethane / 1 h / 0 - 20 °C
3: sodium azide / N,N-dimethyl-formamide / 20 °C
4: triphenylphosphine / tetrahydrofuran; water / 4 h / 70 °C
With sodium azide; sodium carbonate; triethylamine; triphenylphosphine; tetrakis(triphenylphosphine) palladium(0); In tetrahydrofuran; dichloromethane; water; N,N-dimethyl-formamide; 1: Suzuki-Miyaura coupling reaction;
DOI:10.1055/s-2006-939059
Guidance literature:
Multi-step reaction with 5 steps
1: 79 percent / aq. K2CO3, Pd(OAc)2 / acetone / Heating
2: 97 percent
3: 1.) n-BuLi / 1.) hexane, RT, 5 min, 2.) THF, hexane, RT, overnight
4: 1.) N-bromosuccinimide, dibenzoyl peroxide, 2.) sodium azide / 1.) CCl4, reflux, 1.5 h, 2.) DMSO, 80 deg C, 4 h
5: 73 percent / H2 / 5percent Pd/BaSO4 / methanol / 760 Torr
With palladium diacetate; N-Bromosuccinimide; n-butyllithium; sodium azide; hydrogen; potassium carbonate; dibenzoyl peroxide; Pd-BaSO4; In methanol; acetone;
DOI:10.1021/jm950414g
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