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674575 Sigma-Aldrich

MacMillan Imidazolidinone OrganoCatalysts Kit I

  •  eCl@ss 32161000

  •  NACRES NA.22

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Description

Packaging

1 kit in glass bottle

Legal Information

U.S. Pat. 6,369,243 and related patents apply. For research purposes only.

Kit component also available separately

Description

Product #

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(5S)-(−)-2,2,3-Trimethyl-5-benzyl-4-imidazolidinone monohydrochloride, 97% 500 mg SDS 569763
(S)-(+)-2-(tert-Butyl)-3-methyl-4-imidazolidinone trifluoroacetic acid, 96% 500 mg SDS 661902
(5S)-(−)-2,2,3-Trimethyl-5-benzyl-4-imidazolidinone dichloroacetic acid, 97% 500 mg SDS 663085
(2S,5S)-(−)-2-tert-Butyl-3-methyl-5-benzyl-4-imidazolidinone, 97% 500 mg SDS 663107
(2S,5S)-(–)-5-Benzyl-3-methyl-2-(5-methyl-2-furyl)-4-imidazolidinone, 95% 250 mg SDS 668540
Safety & Documentation

Safety Information

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Signal word 
Danger
Hazard statements 
Precautionary statements 
RIDADR 
UN 3316 9

Documents

Certificate of Analysis (COA)

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Protocols & Articles

Articles

MacMillan Imidazolidinone OrganoCatalysts™ | Aldrich ChemFiles 2007, 7.9, 8.

Developed by Professor David MacMillan at Caltech, imidazolidinone based OrganoCatalysts™ are designed to serve as general catalysts for a myriad of asymmetric transformations. The first highly enant...
Aldrich ChemFiles 2007, 7.9, 8.
Keywords: Alkylations, Asymmetric synthesis, Chemfiles, Chlorinations, Condensations, Cycloadditions, Fluorinations, Formulations, Hydrogenations, Reductions

Related Content

Macmillan Imidazolidinone Organocatalysts in Chemical Sythesis

Developed by Professor David MacMillan at Caltech, imidazolidinone-based OrganoCatalysts are designed to serve as general catalysts for a variety of asymmetric transformations. The first highly enant...
Keywords: Alkylations, Asymmetric catalysis, Asymmetric synthesis, Catalysis, Chlorinations, Condensations, Cycloadditions, Diels-Alder reaction, Fluorinations, Friedel-Crafts Alkylation

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