methyl rel-(1R,2R)-2-(4-aminophenyl)cyclopropanecarboxylate

Base Information

Chemical Name:methyl rel-(1R,2R)-2-(4-aminophenyl)cyclopropanecarboxylate
CAS No.:1356600-10-6
Molecular Formula:C₁₁H₁₃NO₂
Molecular Weight:191.23
Hs Code.:

Synonyms:methyl rel-(1R,2R)-2-(4-aminophenyl)cyclopropanecarboxylate

Suppliers and Price of methyl rel-(1R,2R)-2-(4-aminophenyl)cyclopropanecarboxylate

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 2 raw suppliers

Chemical Property of methyl rel-(1R,2R)-2-(4-aminophenyl)cyclopropanecarboxylate

Chemical Property:

Purity/Quality:: 99% ^*data from raw suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Technology Process of methyl rel-(1R,2R)-2-(4-aminophenyl)cyclopropanecarboxylate

There total 3 articles about methyl rel-(1R,2R)-2-(4-aminophenyl)cyclopropanecarboxylate 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: 33.1%

: 1356600-09-3
methyl (1R,2R)-2-(4-nitrophenyl)cyclopropanecarboxylate

: 1356600-10-6
methyl rel-(1R,2R)-2-(4-aminophenyl)cyclopropanecarboxylate

Guidance literature:: With hydrogen; palladium 10% on activated carbon; In ethyl acetate; at 20 ℃; for 5h; under 2068.65 Torr;

Reference yield:

: 1356600-07-1
trans-2-(4-nitrophenyl)cyclopropane-1-carboxylic acid

: 1356600-10-6
methyl rel-(1R,2R)-2-(4-aminophenyl)cyclopropanecarboxylate

Guidance literature:: Multi-step reaction with 2 steps

1: potassium carbonate / N,N-dimethyl-formamide / 8 h / 20 °C

2: hydrogen / palladium 10% on activated carbon / ethyl acetate / 5 h / 20 °C / 2068.65 Torr

With hydrogen; potassium carbonate; palladium 10% on activated carbon; In ethyl acetate; N,N-dimethyl-formamide;

Reference yield:

: 3471-10-1
(1R,2R)-trans-2-phenyl-1-cyclopropanecarboxylic acid

: 1356600-10-6
methyl rel-(1R,2R)-2-(4-aminophenyl)cyclopropanecarboxylate

Guidance literature:: Multi-step reaction with 3 steps

1: nitric acid / 3.5 h / 0 - 20 °C

2: potassium carbonate / N,N-dimethyl-formamide / 8 h / 20 °C

3: hydrogen / palladium 10% on activated carbon / ethyl acetate / 5 h / 20 °C / 2068.65 Torr

With hydrogen; nitric acid; potassium carbonate; palladium 10% on activated carbon; In ethyl acetate; N,N-dimethyl-formamide;