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Ethyl 1-bromocyclobutanecarboxylate

Base Information Edit
  • Chemical Name:Ethyl 1-bromocyclobutanecarboxylate
  • CAS No.:35120-18-4
  • Molecular Formula:C7H11 Br O2
  • Molecular Weight:207.067
  • Hs Code.:29162000
  • European Community (EC) Number:252-384-6
  • NSC Number:135010
  • UNII:AX1RMD8FYJ
  • DSSTox Substance ID:DTXSID90188624
  • Nikkaji Number:J321B
  • Wikidata:Q72453880
  • Mol file:35120-18-4.mol
Ethyl 1-bromocyclobutanecarboxylate

Synonyms:Ethyl 1-bromocyclobutanecarboxylate;35120-18-4;ethyl 1-bromocyclobutane-1-carboxylate;Ethyl alpha-bromocyclobutanecarboxylate;1-Bromocyclobutanecarboxylic acid ethyl ester;Cyclobutanecarboxylic acid, 1-bromo-, ethyl ester;C7H11BrO2;1-bromo-cyclobutanecarboxylic acid ethyl ester;AX1RMD8FYJ;EINECS 252-384-6;NSC-135010;Ethyl .alpha.-bromocyclobutanecarboxylate;UNII-AX1RMD8FYJ;ethyl 1-bromocyclobutanoate;SCHEMBL311023;Ethyl abromocyclobutanecarboxylate;DTXSID90188624;Ethyl1-bromocyclobutanecarboxylate;ethyl-1-bromocyclobutanecarboxylate;1-Ethoxycarbonyl-1-bromocyclobutane;AMY23810;ethyl 1-bromocyclobutane carboxylate;ethyl 1-bromocyclobutane-carboxylate;ethyl-1-bromocyclobutane carboxylate;Ethyl alphabromocyclobutanecarboxylate;MFCD00001322;NSC135010;AKOS015907699;1-Bromocyclobutanecarboxylic acid ethyl;Ethyl 1-bromo-1-cyclobutanecarboxylate;NSC 135010;SB40674;AC-29239;CS-10159;Ethyl 1-bromocyclobutanecarboxylate, 96%;CS-0034793;E1245;FT-0682770;EN300-207470;A874760;J-019952

Suppliers and Price of Ethyl 1-bromocyclobutanecarboxylate
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
  • TRC
  • Ethyl 1-bromocyclobutanecarboxylate
  • 1g
  • $ 90.00
  • TCI Chemical
  • Ethyl 1-Bromocyclobutanecarboxylate >96.0%(GC)
  • 5g
  • $ 134.00
  • TCI Chemical
  • Ethyl 1-Bromocyclobutanecarboxylate >96.0%(GC)
  • 1g
  • $ 34.00
  • SynQuest Laboratories
  • Ethyl 1-bromocyclobutanecarboxylate 97%
  • 25 g
  • $ 205.00
  • SynQuest Laboratories
  • Ethyl 1-bromocyclobutanecarboxylate 97%
  • 1 g
  • $ 40.00
  • SynQuest Laboratories
  • Ethyl 1-bromocyclobutanecarboxylate 97%
  • 5 g
  • $ 80.00
  • Sigma-Aldrich
  • Ethyl 1-bromocyclobutanecarboxylate 96%
  • 5g
  • $ 131.00
  • Matrix Scientific
  • Ethyl alpha-bromocyclobutanecarboxylate 95+%
  • 1g
  • $ 114.00
  • Matrix Scientific
  • Ethyl alpha-bromocyclobutanecarboxylate 95+%
  • 5g
  • $ 473.00
  • Matrix Scientific
  • Ethyl alpha-bromocyclobutanecarboxylate 95+%
  • 10g
  • $ 805.00
Total 46 raw suppliers
Chemical Property of Ethyl 1-bromocyclobutanecarboxylate Edit
Chemical Property:
  • Vapor Pressure:0.387mmHg at 25°C 
  • Refractive Index:n20/D 1.471(lit.) 
  • Boiling Point:197°Cat760mmHg 
  • Flash Point:79.4°C 
  • PSA:26.30000 
  • Density:1.501g/cm3 
  • LogP:1.86710 
  • Storage Temp.:2-8°C 
  • XLogP3:2
  • Hydrogen Bond Donor Count:0
  • Hydrogen Bond Acceptor Count:2
  • Rotatable Bond Count:3
  • Exact Mass:205.99424
  • Heavy Atom Count:10
  • Complexity:141
Purity/Quality:

98% *data from raw suppliers

Ethyl 1-bromocyclobutanecarboxylate *data from reagent suppliers

Safty Information:
  • Pictogram(s):  
  • Hazard Codes:
  • Statements: 34 
  • Safety Statements: 26-27-36/37/39-45 
MSDS Files:

SDS file from LookChem

Total 1 MSDS from other Authors

Useful:
  • Canonical SMILES:CCOC(=O)C1(CCC1)Br
  • Uses Ethyl 1-bromocyclobutanecarboxylate was used in the synthesis of 1?aminocyclobutane carboxylic acid.
Technology Process of Ethyl 1-bromocyclobutanecarboxylate

There total 3 articles about Ethyl 1-bromocyclobutanecarboxylate 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 N-Bromosuccinimide; 2,2'-azobis(isobutyronitrile); In tetrachloromethane; for 4h; Reflux; Inert atmosphere;
DOI:10.1021/jo302308q
Guidance literature:
With tetra-N-butylammonium tribromide; dibromoisocyanuric acid; In dichloromethane; at 20 ℃; for 4h; UV-irradiation;
Guidance literature:
With phosphorus; thionyl chloride; bromine; ueber mehrere Stufen;
DOI:10.1039/jr9530003002
Refernces Edit
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