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(1S,2S)-Diethyl cyclopropane-1,2-dicarboxylate

Base Information
  • Chemical Name:(1S,2S)-Diethyl cyclopropane-1,2-dicarboxylate
  • CAS No.:889461-57-8
  • Molecular Formula:C9H14O4
  • Molecular Weight:186.208
  • Hs Code.:
  • Mol file:889461-57-8.mol
(1S,2S)-Diethyl cyclopropane-1,2-dicarboxylate

Synonyms:

Suppliers and Price of (1S,2S)-Diethyl cyclopropane-1,2-dicarboxylate
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
  • (1S,?2S)?-1,?2-?Cyclopropanedicarbox?ylicAcid1,?2-?DiethylEster
  • 1g
  • $ 340.00
  • TRC
  • (1S,?2S)?-1,?2-?Cyclopropanedicarbox?ylicAcid1,?2-?DiethylEster
  • 5g
  • $ 1670.00
  • Crysdot
  • (1S,2S)-Diethylcyclopropane-1,2-dicarboxylate 95+%
  • 1g
  • $ 1042.00
Total 6 raw suppliers
Chemical Property of (1S,2S)-Diethyl cyclopropane-1,2-dicarboxylate
Chemical Property:
  • Storage Temp.:-20°C Freezer 
  • Solubility.:Dichloromethane; Ethyl Acetate; Methanol 
Purity/Quality:

99%, *data from raw suppliers

(1S,?2S)?-1,?2-?Cyclopropanedicarbox?ylicAcid1,?2-?DiethylEster *data from reagent suppliers

Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:
Useful:
  • Uses (1S,?2S)?-1,?2-?Cyclopropanedicarbox?ylic Acid 1,?2-?Diethyl Ester is an intermediate in synthesizing (O846925), (2S,3S)-2,3-Oxiranedicarboxylic Acid Monoethyl Ester is used in the synthesis of aza-peptidyl inhibitors of lysosomal asparaginyl endopeptidase, legumain. Also used in the synthesis of irreversible epidermal growth factor receptor inhibitors and probes for cathespins.
Technology Process of (1S,2S)-Diethyl cyclopropane-1,2-dicarboxylate

There total 4 articles about (1S,2S)-Diethyl cyclopropane-1,2-dicarboxylate 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 water; sodium hydroxide; at 28 ℃; pH=7; aq. phosphate buffer; Enzymatic reaction;
DOI:10.1039/b812777h
Guidance literature:
With (1,5-cyclooctadiene)(pyridine)(tricyclohexylphosphine)iridium (I) hexafluorophosphate; In dichloromethane; at 20 ℃; for 12h; stereoselective reaction; Inert atmosphere;
DOI:10.1002/anie.201300468
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