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Carbamic acid, (4-hydroxy-2-cyclopenten-1-yl)-, 1,1-dimethylethyl ester (9CI)

Base Information
  • Chemical Name:Carbamic acid, (4-hydroxy-2-cyclopenten-1-yl)-, 1,1-dimethylethyl ester (9CI)
  • CAS No.:657396-96-8
  • Molecular Formula:C10H17NO3
  • Molecular Weight:199.24700
  • Hs Code.:
  • Mol file:657396-96-8.mol
Carbamic acid, (4-hydroxy-2-cyclopenten-1-yl)-, 1,1-dimethylethyl ester (9CI)

Synonyms:(4-hydroxycyclopent-2-enyl)carbamic acid tert-butyl ester;

Suppliers and Price of Carbamic acid, (4-hydroxy-2-cyclopenten-1-yl)-, 1,1-dimethylethyl ester (9CI)
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
  • J&W Pharmlab
  • (4-Hydroxy-cyclopent-2-enyl)-carbamicacidtert-butylester 97%
  • 5g
  • $ 1998.00
  • J&W Pharmlab
  • (4-Hydroxy-cyclopent-2-enyl)-carbamicacidtert-butylester 97%
  • 1g
  • $ 598.00
  • J&W Pharmlab
  • (4-Hydroxy-cyclopent-2-enyl)-carbamicacidtert-butylester 97%
  • 500mg
  • $ 349.00
Total 2 raw suppliers
Chemical Property of Carbamic acid, (4-hydroxy-2-cyclopenten-1-yl)-, 1,1-dimethylethyl ester (9CI)
Chemical Property:
  • PSA:58.56000 
  • LogP:1.59140 
Purity/Quality:

97% *data from raw suppliers

(4-Hydroxy-cyclopent-2-enyl)-carbamicacidtert-butylester 97% *data from reagent suppliers

Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:
Useful:
Technology Process of Carbamic acid, (4-hydroxy-2-cyclopenten-1-yl)-, 1,1-dimethylethyl ester (9CI)

There total 4 articles about Carbamic acid, (4-hydroxy-2-cyclopenten-1-yl)-, 1,1-dimethylethyl ester (9CI) 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:
2-oxa-3-azabicyclo[2.2.1]hept-5-ene-3-carboxylic acidtert-butyl ester; With molybdenum hexacarbonyl; In water; acetonitrile; at 20 ℃; for 0.166667h;
With sodium tetrahydroborate; In water; acetonitrile; for 3h; Heating / reflux;
Guidance literature:
Multi-step reaction with 2 steps
1: 79 percent / tetra-n-butylammonium periodate / CH2Cl2 / 1 h / 20 °C
2: disodium hydrogen phosphate; sodium amalgam / ethanol / 1.5 h / 0 °C
With disodium hydrogenphosphate; sodium amalgam; tetrabutylammonium periodite; In ethanol; dichloromethane;
DOI:10.1016/j.tet.2004.01.046
Guidance literature:
Multi-step reaction with 3 steps
1: 89 percent / hydroxylamine hydrochloride; sodium carbonate / diethyl ether; H2O / 0 - 20 °C
2: 79 percent / tetra-n-butylammonium periodate / CH2Cl2 / 1 h / 20 °C
3: disodium hydrogen phosphate; sodium amalgam / ethanol / 1.5 h / 0 °C
With disodium hydrogenphosphate; sodium amalgam; hydroxylamine hydrochloride; sodium carbonate; tetrabutylammonium periodite; In diethyl ether; ethanol; dichloromethane; water;
DOI:10.1016/j.tet.2004.01.046
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