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3-(Methoxycarbonyl)bicyclo[1.1.1]pentane-1-carboxylic acid

Base Information
  • Chemical Name:3-(Methoxycarbonyl)bicyclo[1.1.1]pentane-1-carboxylic acid
  • CAS No.:83249-10-9
  • Molecular Formula:C8H10O4
  • Molecular Weight:170.165
  • Hs Code.:2917198090
  • European Community (EC) Number:810-718-3
  • Nikkaji Number:J516.178I
  • Mol file:83249-10-9.mol
3-(Methoxycarbonyl)bicyclo[1.1.1]pentane-1-carboxylic acid

Synonyms:83249-10-9;3-(methoxycarbonyl)bicyclo[1.1.1]pentane-1-carboxylic acid;3-methoxycarbonylbicyclo[1.1.1]pentane-1-carboxylic acid;Bicyclo[1.1.1]pentane-1,3-dicarboxylic acid monoMethyl ester;MFCD20638314;3-Methoxycarbonylbicyclo-[1.1.1]pentane-1-carboxylic acid;SCHEMBL9143861;SCHEMBL20851067;SCHEMBL20851079;UJZHYIMESNWEQA-UHFFFAOYSA-N;AMY12281;AKOS024255979;CS-W001056;GS-8008;SB38921;SY042099;M3149;EN300-132008;EN300-19052195;Z1262511436;3-(methoxycarbonyl)bicyclo<1.1.1>pentane-1-carboxylic acid;3-(methoxycarbonyl)bicyclo[1.1.1]pentane-1-carboxylicacid;Bicyclo[1.1.1]pentane-1,3-dicarboxylic acid, 1-methyl ester;Bicyclo[1.1.1]pentane-1,3-dicarboxylic acid, 1-methyl ester, AldrichCPR

Suppliers and Price of 3-(Methoxycarbonyl)bicyclo[1.1.1]pentane-1-carboxylic acid
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
  • Bicyclo[1.1.1]pentane-1,3-dicarboxylicAcid,1-methylEster
  • 250mg
  • $ 875.00
  • TRC
  • Bicyclo[1.1.1]pentane-1,3-dicarboxylicAcid,1-methylEster
  • 5mg
  • $ 50.00
  • TCI Chemical
  • 3-(Methoxycarbonyl)bicyclo[1.1.1]pentane-1-carboxylic Acid
  • 200MG
  • $ 166.00
  • TCI Chemical
  • 3-(Methoxycarbonyl)bicyclo[1.1.1]pentane-1-carboxylic Acid
  • 1G
  • $ 497.00
  • SynQuest Laboratories
  • 3-(Methoxycarbonyl)bicyclo[1.1.1]pentane-1-carboxylic acid 97.0%
  • 1 g
  • $ 890.00
  • Oakwood
  • 3-(Methoxycarbonyl)bicyclo[1.1.1]pentane-1-carboxylic acid
  • 250mg
  • $ 35.00
  • Oakwood
  • 3-(Methoxycarbonyl)bicyclo[1.1.1]pentane-1-carboxylic acid
  • 1g
  • $ 70.00
  • Matrix Scientific
  • 3-(Methoxycarbonyl)bicyclo[1.1.1]pentane-1-carboxylic Acid 97.0%
  • 1g
  • $ 530.00
  • J&W Pharmlab
  • Bicyclo[1.1.1]pentane-1,3-dicarboxylicacidmonomethylester 96%
  • 1g
  • $ 398.00
  • J&W Pharmlab
  • Bicyclo[1.1.1]pentane-1,3-dicarboxylicacidmonomethylester 96%
  • 5g
  • $ 1590.00
Total 35 raw suppliers
Chemical Property of 3-(Methoxycarbonyl)bicyclo[1.1.1]pentane-1-carboxylic acid
Chemical Property:
  • Melting Point:138-139 °C(Solv: chloroform (67-66-3); heptane (142-82-5)) 
  • Boiling Point:272.2±40.0 °C(Predicted) 
  • PKA:4.50±0.40(Predicted) 
  • PSA:66.43000 
  • Density:1.559±0.06 g/cm3(Predicted) 
  • LogP:-0.92040 
  • Storage Temp.:2-8°C 
  • XLogP3:-0.1
  • Hydrogen Bond Donor Count:1
  • Hydrogen Bond Acceptor Count:4
  • Rotatable Bond Count:3
  • Exact Mass:170.05790880
  • Heavy Atom Count:12
  • Complexity:249
Purity/Quality:

99%, *data from raw suppliers

Bicyclo[1.1.1]pentane-1,3-dicarboxylicAcid,1-methylEster *data from reagent suppliers

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

SDS file from LookChem

Useful:
  • Canonical SMILES:COC(=O)C12CC(C1)(C2)C(=O)O
  • Uses Bicyclo[1.1.1]pentane-1,3-dicarboxylic Acid, 1-methyl Ester acts as a reagent for the synthesis and in the biopharmaceutical evaluation of imatinib analogs. Also functions as a reagent for the preparation and in biological evaluation of novel bicyclo[1.1.1]pentane-based acidic amino acids as glutamate receptors ligands It is a COVID19-related research product.
Technology Process of 3-(Methoxycarbonyl)bicyclo[1.1.1]pentane-1-carboxylic acid

There total 14 articles about 3-(Methoxycarbonyl)bicyclo[1.1.1]pentane-1-carboxylic acid 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 lithium hydroxide monohydrate; In tetrahydrofuran; at 50 ℃; for 72h;
DOI:10.1021/acs.joc.1c00977
Guidance literature:
monomethyl oxalyl chloride; [1.1.1]propellane; In diethyl ether; at -80 - 0 ℃;
With water; for 2h; Alkaline conditions;
Guidance literature:
With ruthenium(IV) oxide; sodium hypochlorite; In tetrachloromethane; for 47h;
DOI:10.1021/jo00146a031
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