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Carbamic acid, (hydroxymethyl)-, 2,3-dihydro-2,2-dimethyl-7-benzofuranyl ester

Base Information
  • Chemical Name:Carbamic acid, (hydroxymethyl)-, 2,3-dihydro-2,2-dimethyl-7-benzofuranyl ester
  • CAS No.:18999-70-7
  • Deprecated CAS:52208-00-1
  • Molecular Formula:C12H15NO4
  • Molecular Weight:237.255
  • Hs Code.:
  • DSSTox Substance ID:DTXSID30172441
  • Nikkaji Number:J855.468D
  • Wikidata:Q83042542
Carbamic acid, (hydroxymethyl)-, 2,3-dihydro-2,2-dimethyl-7-benzofuranyl ester

Synonyms:N-Hydroxymethylcarbofuran;BRN 1380621;CARBAMIC ACID, (HYDROXYMETHYL)-, 2,3-DIHYDRO-2,2-DIMETHYL-7-BENZOFURANYL ESTER;(Hydroxymethyl)carbamic acid 2,3-dihydro-2,2-dimethyl-7-benzofuranyl ester;18999-70-7;DTXSID30172441;LS-49941;N-(Hydroxymethyl)carbamic acid (2,2-dimethyl-2,3-dihydrobenzofuran)-7-yl ester

Suppliers and Price of Carbamic acid, (hydroxymethyl)-, 2,3-dihydro-2,2-dimethyl-7-benzofuranyl ester
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The product has achieved commercial mass production*data from LookChem market partment
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Chemical Property of Carbamic acid, (hydroxymethyl)-, 2,3-dihydro-2,2-dimethyl-7-benzofuranyl ester
Chemical Property:
  • Vapor Pressure:6.11E-06mmHg at 25°C 
  • XLogP3:1.7
  • Hydrogen Bond Donor Count:2
  • Hydrogen Bond Acceptor Count:4
  • Rotatable Bond Count:3
  • Exact Mass:237.10010796
  • Heavy Atom Count:17
  • Complexity:292
Purity/Quality:
Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:
Useful:
  • Canonical SMILES:CC1(CC2=C(O1)C(=CC=C2)OC(=O)NCO)C
Technology Process of Carbamic acid, (hydroxymethyl)-, 2,3-dihydro-2,2-dimethyl-7-benzofuranyl ester

There total 4 articles about Carbamic acid, (hydroxymethyl)-, 2,3-dihydro-2,2-dimethyl-7-benzofuranyl ester 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:
Multi-step reaction with 2 steps
1: 66 percent / Et3N / benzene / 18 h / Heating
2: 50 percent / Me3SiI / CCl4 / 1 h
With trimethylsilyl iodide; triethylamine; In tetrachloromethane; benzene;
DOI:10.1021/jf980347+
Guidance literature:
Multi-step reaction with 3 steps
1: 77 percent / KOH / ethanol
2: 66 percent / Et3N / benzene / 18 h / Heating
3: 50 percent / Me3SiI / CCl4 / 1 h
With potassium hydroxide; trimethylsilyl iodide; triethylamine; In tetrachloromethane; ethanol; benzene;
DOI:10.1021/jf980347+
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