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(1S,3R,4R)-3-(Boc-aMino)-4-hydroxy-cyclohexanecarboxylic acid ethyl ester

Base Information
  • Chemical Name:(1S,3R,4R)-3-(Boc-aMino)-4-hydroxy-cyclohexanecarboxylic acid ethyl ester
  • CAS No.:365997-33-7
  • Molecular Formula:C14H25NO5
  • Molecular Weight:287.356
  • Hs Code.:
  • Mol file:365997-33-7.mol
(1S,3R,4R)-3-(Boc-aMino)-4-hydroxy-cyclohexanecarboxylic acid ethyl ester

Synonyms:(1S,3R,4R)-3-[(tert-butoxycarbonyl)amino]-4-hydroxycyclohexanecarboxylic acid ethyl ester;ethyl (1S,3R,4R)-3-[(t-butoxycarbonyl)amino]-4-hydroxycyclohexanecarboxylate;Ethyl (1S,3R,4R)-3-(tert-butoxycarbonylamino)-4-hydroxycyclohexane-1-carboxylate;ethyl (1S,3R,4R)-3-[(tert-butoxycarbonyl)amino]-4-hydroxycyclohexanecarboxylate;

Suppliers and Price of (1S,3R,4R)-3-(Boc-aMino)-4-hydroxy-cyclohexanecarboxylic acid ethyl ester
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
  • TRC
  • Ethyl(1S,3R,4R)-3-(tert-butoxycarbonylamino)-4-hydroxycyclohexane-1-carboxylate
  • 2.5g
  • $ 60.00
  • Matrix Scientific
  • (1S,3R,4R)-3-(Boc-amino)-4-hydroxy-cyclohexanecarboxylicacidethylester 97.0%
  • 1g
  • $ 1073.00
  • Crysdot
  • (1S,3R,4R)-Ethyl3-((tert-butoxycarbonyl)amino)-4-hydroxycyclohexanecarboxylate 95+%
  • 1g
  • $ 668.00
  • Chemenu
  • (1S,3R,4R)-3-(Boc-aMino)-4-hydroxy-cyclohexanecarboxylicacidethylester 97%
  • 100g
  • $ 418.00
  • American Custom Chemicals Corporation
  • (1S,3R,4R)-3-(BOC-AMINO)-4-HYDROXY-CYCLOHEXANECARBOXYLIC ACID ETHYL ESTER 95.00%
  • 5MG
  • $ 499.94
  • Ambeed
  • (1S,3R,4R)-Ethyl3-((tert-butoxycarbonyl)amino)-4-hydroxycyclohexanecarboxylate 97+%
  • 5g
  • $ 29.00
  • Ambeed
  • (1S,3R,4R)-Ethyl3-((tert-butoxycarbonyl)amino)-4-hydroxycyclohexanecarboxylate 97+%
  • 100g
  • $ 176.00
  • Ambeed
  • (1S,3R,4R)-Ethyl3-((tert-butoxycarbonyl)amino)-4-hydroxycyclohexanecarboxylate 97+%
  • 25g
  • $ 90.00
  • AK Scientific
  • (1S,3R,4R)-3-(Boc-amino)-4-hydroxy-cyclohexanecarboxylicacidethylester
  • 100g
  • $ 691.00
  • AK Scientific
  • (1S,3R,4R)-3-(Boc-amino)-4-hydroxy-cyclohexanecarboxylicacidethylester
  • 10g
  • $ 184.00
Total 47 raw suppliers
Chemical Property of (1S,3R,4R)-3-(Boc-aMino)-4-hydroxy-cyclohexanecarboxylic acid ethyl ester
Chemical Property:
  • Melting Point:93-95°C 
  • Boiling Point:406.6±45.0 °C(Predicted) 
  • PKA:11.73±0.60(Predicted) 
  • PSA:84.86000 
  • Density:1.12±0.1 g/cm3(Predicted) 
  • LogP:1.99470 
  • Storage Temp.:Refrigerator 
  • Solubility.:Chloroform (Sparingly), DMSO (Slightly), Ethyl Acetate (Slightly) 
Purity/Quality:

99% *data from raw suppliers

Ethyl(1S,3R,4R)-3-(tert-butoxycarbonylamino)-4-hydroxycyclohexane-1-carboxylate *data from reagent suppliers

Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:

SDS file from LookChem

Useful:
  • Uses Ethyl (1S,3R,4R)-3-(tert-butoxycarbonylamino)-4-hydroxycyclohexane-1-carboxylate, is a building block used in various chemicla synthesis. It can be used for the preparation of six stereoisomers of diaminocyclohexane carboxamide as key intermediates for synthesis of factor Xa inhibitors.
Technology Process of (1S,3R,4R)-3-(Boc-aMino)-4-hydroxy-cyclohexanecarboxylic acid ethyl ester

There total 15 articles about (1S,3R,4R)-3-(Boc-aMino)-4-hydroxy-cyclohexanecarboxylic acid ethyl 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:
(1S,3S,6R)-7-oxabicyclo[4.1.0]heptane-3-carboxylic acid ethyl ester; With ammonia; In water; at 45 ℃;
di-tert-butyl dicarbonate; In ethanol; at 20 ℃;
DOI:10.1016/j.bmcl.2020.126969
Guidance literature:
Multi-step reaction with 5 steps
1.1: sodium hydrogencarbonate; potassium iodide / dichloromethane / 0.17 h
1.2: 2 h / 20 °C
2.1: 0.17 h / 20 °C
2.2: 3 h
3.1: ammonium hydroxide / ethanol / 4 h / 40 °C
4.1: potassium carbonate / ethyl acetate / 5 h / 20 °C
5.1: vinyl acetate / di-isopropyl ether / 18 h / 45 °C / Enzymatic reaction
With ammonium hydroxide; vinyl acetate; sodium hydrogencarbonate; potassium carbonate; potassium iodide; In ethanol; dichloromethane; di-isopropyl ether; ethyl acetate;
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