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Carbamic acid, [2-(2-methoxyphenyl)cyclopropyl]-, 1,1-dimethylethyl ester, (1R-trans)-

Base Information
  • Chemical Name:Carbamic acid, [2-(2-methoxyphenyl)cyclopropyl]-, 1,1-dimethylethyl ester, (1R-trans)-
  • CAS No.:157518-47-3
  • Molecular Formula:C15H21NO3
  • Molecular Weight:263.337
  • Hs Code.:
  • DSSTox Substance ID:DTXSID001126544
Carbamic acid, [2-(2-methoxyphenyl)cyclopropyl]-, 1,1-dimethylethyl ester, (1R-trans)-

Synonyms:DTXSID001126544;Carbamic acid, [2-(2-methoxyphenyl)cyclopropyl]-, 1,1-dimethylethyl ester, (1R-trans)-;157518-47-3

Suppliers and Price of Carbamic acid, [2-(2-methoxyphenyl)cyclopropyl]-, 1,1-dimethylethyl ester, (1R-trans)-
Supply Marketing:
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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, [2-(2-methoxyphenyl)cyclopropyl]-, 1,1-dimethylethyl ester, (1R-trans)-
Chemical Property:
  • XLogP3:2.8
  • Hydrogen Bond Donor Count:1
  • Hydrogen Bond Acceptor Count:3
  • Rotatable Bond Count:5
  • Exact Mass:263.15214353
  • Heavy Atom Count:19
  • Complexity:324
Purity/Quality:
Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:
Useful:
  • Canonical SMILES:CC(C)(C)OC(=O)NC1CC1C2=CC=CC=C2OC
  • Isomeric SMILES:CC(C)(C)OC(=O)N[C@@H]1C[C@H]1C2=CC=CC=C2OC
Technology Process of Carbamic acid, [2-(2-methoxyphenyl)cyclopropyl]-, 1,1-dimethylethyl ester, (1R-trans)-

There total 6 articles about Carbamic acid, [2-(2-methoxyphenyl)cyclopropyl]-, 1,1-dimethylethyl ester, (1R-trans)- 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 6 steps
1: SOCl2 / 2 h / Ambient temperature
2: 1.) NaH / 1) toluene, 30 min; 2) toluene, overnight
3: 73 percent / Pd(OAc)2 / CH2Cl2 / 3 h / 0 - 5 °C
4: 1.) titanium(IV) isopropoxide, benzyl alcohol, 2.) aq. NaOH / 1) 150 deg C, 30 min; 2) THF, MeOH, 2 h
5: 1.) ethyl chloroformate, Et3N, 2.) aq. NaN3 / 1) -10 deg C, acetone, 2 h; 2) -10 deg C, acetone, 1 h
6: 1) toluene, 90 deg C, 3 h; 2) reflux, 16 h
With titanium(IV) isopropylate; palladium diacetate; sodium hydroxide; thionyl chloride; sodium azide; chloroformic acid ethyl ester; sodium hydride; triethylamine; benzyl alcohol; In dichloromethane;
Guidance literature:
Multi-step reaction with 5 steps
1: 1.) NaH / 1) toluene, 30 min; 2) toluene, overnight
2: 73 percent / Pd(OAc)2 / CH2Cl2 / 3 h / 0 - 5 °C
3: 1.) titanium(IV) isopropoxide, benzyl alcohol, 2.) aq. NaOH / 1) 150 deg C, 30 min; 2) THF, MeOH, 2 h
4: 1.) ethyl chloroformate, Et3N, 2.) aq. NaN3 / 1) -10 deg C, acetone, 2 h; 2) -10 deg C, acetone, 1 h
5: 1) toluene, 90 deg C, 3 h; 2) reflux, 16 h
With titanium(IV) isopropylate; palladium diacetate; sodium hydroxide; sodium azide; chloroformic acid ethyl ester; sodium hydride; triethylamine; benzyl alcohol; In dichloromethane;
Guidance literature:
Multi-step reaction with 4 steps
1: 73 percent / Pd(OAc)2 / CH2Cl2 / 3 h / 0 - 5 °C
2: 1.) titanium(IV) isopropoxide, benzyl alcohol, 2.) aq. NaOH / 1) 150 deg C, 30 min; 2) THF, MeOH, 2 h
3: 1.) ethyl chloroformate, Et3N, 2.) aq. NaN3 / 1) -10 deg C, acetone, 2 h; 2) -10 deg C, acetone, 1 h
4: 1) toluene, 90 deg C, 3 h; 2) reflux, 16 h
With titanium(IV) isopropylate; palladium diacetate; sodium hydroxide; sodium azide; chloroformic acid ethyl ester; triethylamine; benzyl alcohol; In dichloromethane;
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