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(5S)-(-)-2,2,3-Trimethyl-5-benzyl-4-imidazolidinone monohydrochloride

Base Information
  • Chemical Name:(5S)-(-)-2,2,3-Trimethyl-5-benzyl-4-imidazolidinone monohydrochloride
  • CAS No.:278173-23-2
  • Molecular Formula:C13H18N2O.HCl
  • Molecular Weight:254.76
  • Hs Code.:2933990090
  • European Community (EC) Number:878-912-0
  • UNII:785PBY3X4M
  • DSSTox Substance ID:DTXSID60431497
  • Mol file:278173-23-2.mol
(5S)-(-)-2,2,3-Trimethyl-5-benzyl-4-imidazolidinone monohydrochloride

Synonyms:278173-23-2;(5S)-(-)-2,2,3-Trimethyl-5-benzyl-4-imidazolidinone monohydrochloride;(S)-5-benzyl-2,2,3-trimethylimidazolidin-4-one hydrochloride;UNII-785PBY3X4M;4-Imidazolidinone, 2,2,3-trimethyl-5-(phenylmethyl)-, hydrochloride (1:1), (5S)-;785PBY3X4M;(5S)-2,2,3-Trimethyl-5-benzyl-4-imidazolidinone hydrochloride;(5S)-5-benzyl-2,2,3-trimethylimidazolidin-4-one;hydrochloride;5-Benzyl-2,2,3-trimethylimidazolidin-4-one hydrochloride, (5S)-;Macmillan's imidazolidinone first generation catalyst hydrochloride;(S)-5-Benzyl-2,2,3-trimethylimidazolidin-4-one hydrochloride, (-)-;4-Imidazolidinone, 2,2,3-trimethyl-5-(phenylmethyl)-, monohydrochloride, (5S)-;Macmillan's imidazolidinone catalysts first generation catalyst hydrochloride [MI];(5S)-5-benzyl-2,2,3-trimethylimidazolidin-4-one hydrochloride;SCHEMBL1262274;DTXSID60431497;YIYFEXGDFJLJGM-MERQFXBCSA-N;MFCD03426983;(5S)-2,2,3-trimethyl-5-phenylmethyl-4-imidazolidinone monohydrochloride;AKOS015844378;CS-15679;CS-0023191;D72546;J-016888;Q27266642;(5S)-5-Benzyl-2,2,3-trimethylimidazolidin-4-one--hydrogen chloride (1/1);(S)-(-)-5-Benzyl-2,2,3-trimethylimidazolidin-4-one hydrochloride salt;(5S)-(-)-2,2,3-Trimethyl-5-benzyl-4-imidazolidinone monohydrochloride, 97%

Suppliers and Price of (5S)-(-)-2,2,3-Trimethyl-5-benzyl-4-imidazolidinone monohydrochloride
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
  • Sigma-Aldrich
  • (5S)-(?)-2,2,3-Trimethyl-5-benzyl-4-imidazolidinone monohydrochloride 97%
  • 2g
  • $ 169.00
  • Sigma-Aldrich
  • (5S)-(?)-2,2,3-Trimethyl-5-benzyl-4-imidazolidinone monohydrochloride 97%
  • 500mg
  • $ 54.80
  • American Custom Chemicals Corporation
  • (5S)-(-)-2,2,3-TRIMETHYL-5-BENZYL-4-IMIDAZOLIDINONE MONOHYDROCHLORIDE 95.00%
  • 2G
  • $ 824.67
  • American Custom Chemicals Corporation
  • (5S)-(-)-2,2,3-TRIMETHYL-5-BENZYL-4-IMIDAZOLIDINONE MONOHYDROCHLORIDE 95.00%
  • 500MG
  • $ 591.34
Total 18 raw suppliers
Chemical Property of (5S)-(-)-2,2,3-Trimethyl-5-benzyl-4-imidazolidinone monohydrochloride
Chemical Property:
  • Vapor Pressure:4.24E-05mmHg at 25°C 
  • Melting Point:157-161 °C(lit.) 
  • Boiling Point:351 °C at 760 mmHg 
  • Flash Point:166.1 °C 
  • PSA:32.34000 
  • LogP:2.46410 
  • Hydrogen Bond Donor Count:2
  • Hydrogen Bond Acceptor Count:2
  • Rotatable Bond Count:2
  • Exact Mass:254.1185909
  • Heavy Atom Count:17
  • Complexity:269
Purity/Quality:

97% *data from raw suppliers

(5S)-(?)-2,2,3-Trimethyl-5-benzyl-4-imidazolidinone monohydrochloride 97% *data from reagent suppliers

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

SDS file from LookChem

Total 1 MSDS from other Authors

Useful:
  • Canonical SMILES:CC1(NC(C(=O)N1C)CC2=CC=CC=C2)C.Cl
  • Isomeric SMILES:CC1(N[C@H](C(=O)N1C)CC2=CC=CC=C2)C.Cl
  • Uses Metal-free OrganoCatalyst technology for asymmetric catalysis. Catalyzes asymmetric Diels-Alder reactions, 1,3-dipolar additions and pyrrole alkylations in high enantiomeric excess.
Technology Process of (5S)-(-)-2,2,3-Trimethyl-5-benzyl-4-imidazolidinone monohydrochloride

There total 3 articles about (5S)-(-)-2,2,3-Trimethyl-5-benzyl-4-imidazolidinone monohydrochloride 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:
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