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ALLYL 5-(BROMOMETHYL)ISOXAZOLE-3-CARBOXYLATE

Base Information
  • Chemical Name:ALLYL 5-(BROMOMETHYL)ISOXAZOLE-3-CARBOXYLATE
  • CAS No.:833445-84-4
  • Molecular Formula:C8H8 Br N O3
  • Molecular Weight:246.06
  • Hs Code.:2934999090
  • Mol file:833445-84-4.mol
ALLYL 5-(BROMOMETHYL)ISOXAZOLE-3-CARBOXYLATE

Synonyms:3-Isoxazolecarboxylicacid, 5-(bromomethyl)-, 2-propenyl ester (9CI)

Suppliers and Price of ALLYL 5-(BROMOMETHYL)ISOXAZOLE-3-CARBOXYLATE
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
  • American Custom Chemicals Corporation
  • ALLYL-5-(BROMOMETHYL)ISOXAZOLE-3-CARBOXYLATE 95.00%
  • 5MG
  • $ 503.06
Total 5 raw suppliers
Chemical Property of ALLYL 5-(BROMOMETHYL)ISOXAZOLE-3-CARBOXYLATE
Chemical Property:
  • PSA:52.33000 
  • LogP:1.91230 
Purity/Quality:

99% *data from raw suppliers

ALLYL-5-(BROMOMETHYL)ISOXAZOLE-3-CARBOXYLATE 95.00% *data from reagent suppliers

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

SDS file from LookChem

Useful:
Technology Process of ALLYL 5-(BROMOMETHYL)ISOXAZOLE-3-CARBOXYLATE

There total 3 articles about ALLYL 5-(BROMOMETHYL)ISOXAZOLE-3-CARBOXYLATE 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 carbon tetrabromide; triphenylphosphine; In dichloromethane; at -20 ℃; for 0.5h;
DOI:10.1016/j.bmcl.2004.09.092
Guidance literature:
Multi-step reaction with 2 steps
1: 76 percent / K2CO3 / dimethylformamide / 7 h / 20 °C
2: 56 percent / PPh3; CBr4 / CH2Cl2 / 0.5 h / -20 °C
With carbon tetrabromide; potassium carbonate; triphenylphosphine; In dichloromethane; N,N-dimethyl-formamide;
DOI:10.1016/j.bmcl.2004.09.092
Guidance literature:
Multi-step reaction with 3 steps
1: 92 percent / Claisen's alkali / methanol / 0.5 h / 0 °C
2: 76 percent / K2CO3 / dimethylformamide / 7 h / 20 °C
3: 56 percent / PPh3; CBr4 / CH2Cl2 / 0.5 h / -20 °C
With carbon tetrabromide; Claisen's alkali; potassium carbonate; triphenylphosphine; In methanol; dichloromethane; N,N-dimethyl-formamide;
DOI:10.1016/j.bmcl.2004.09.092
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