n-benzoyl-alpha-phenylethylamine

US Patent # 3 965 121 Salts of the gamma

Salts of the gamma -lactone of (-)-threo-hydroxycitric acid with R(+)- alpha -methyl-p-nitrobenzylamine Abstract Racemic organic carboxylic acids are efficiently resolved into their enantiomers with antipodes of alpha -methyl-p-nitrobenzylamine

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US Patent # 6 320 069 Production of optically active

Production of optically active ketone Abstract Process for producing an optically active ester by reaction of a racemic alcohol with an optically active amino or tartaric acid derivative a process for producing an optically active alcohol by hydrolysis of the optically active ester a process for converting an alcohol into a ketone by oxidation a method for stably storing an optically

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(R)

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(S)

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US Patent # 6 320 069 Production of optically active

Production of optically active ketone Abstract Process for producing an optically active ester by reaction of a racemic alcohol with an optically active amino or tartaric acid derivative a process for producing an optically active alcohol by hydrolysis of the optically active ester a process for converting an alcohol into a ketone by oxidation a method for stably storing an optically

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(R)

Visit ChemicalBook To find more (R)-(+)-N-BENZOYL-ALPHA-METHYLBENZYLAMINE(20826-48-6) information like chemical properties Structure melting point boiling point density molecular formula molecular weight physical properties toxicity information customs codes You can also browse global suppliers vendor prices Price manufacturers of (R)-(+)-N-BENZOYL-ALPHA

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(R)

Visit ChemicalBook To find more (R)-(+)-N-BENZOYL-ALPHA-METHYLBENZYLAMINE(20826-48-6) information like chemical properties Structure melting point boiling point density molecular formula molecular weight physical properties toxicity information customs codes You can also browse global suppliers vendor prices Price manufacturers of (R)-(+)-N-BENZOYL-ALPHA

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US Patent # 6 320 069 Production of optically active

Production of optically active ketone Abstract Process for producing an optically active ester by reaction of a racemic alcohol with an optically active amino or tartaric acid derivative a process for producing an optically active alcohol by hydrolysis of the optically active ester a process for converting an alcohol into a ketone by oxidation a method for stably storing an optically

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US Patent # 6 320 069 Production of optically active

Production of optically active ketone Abstract Process for producing an optically active ester by reaction of a racemic alcohol with an optically active amino or tartaric acid derivative a process for producing an optically active alcohol by hydrolysis of the optically active ester a process for converting an alcohol into a ketone by oxidation a method for stably storing an optically

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aminum MoleculesGNU

aminum Molecules Structural Archive and Gallery 1H-Purine-2 6-dione 3 7-dihydro-1 3-dimethyl- compd with 1 2-ethanediamine (2:1) 3-AMINO-3-PICOLINE 317-34-0 Aminocardol Aminodur Aminophyllin Aminophylline Ammophyllin BY 108 Cardiofilina Cardiomin Cardophylin Cardophyllin Carena Cariomin DOBO Diaphylline Diophllin Diuxanthine Dura-Tab S M Aminophylline

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US Patent # 3 965 121 Salts of the gamma

Salts of the gamma -lactone of (-)-threo-hydroxycitric acid with R(+)- alpha -methyl-p-nitrobenzylamine Abstract Racemic organic carboxylic acids are efficiently resolved into their enantiomers with antipodes of alpha -methyl-p-nitrobenzylamine

Get More

US3857889A

A general process for the isolation of an enantiomer present in excess in a partially resolved mixture of enantiomers of an organic compound which forms a racemic compound comprising treating the mixture with a crystallisation solvent and a solubilising agent whereby only the enantiomer present in excess passes into solution and is thereby separated from the insoluble

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(R)

Visit ChemicalBook To find more (R)-(+)-N-BENZOYL-ALPHA-METHYLBENZYLAMINE(20826-48-6) information like chemical properties Structure melting point boiling point density molecular formula molecular weight physical properties toxicity information customs codes You can also browse global suppliers vendor prices Price manufacturers of (R)-(+)-N-BENZOYL-ALPHA

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(S)

Visit ChemicalBook To find more (S)-(-)-N-BENZOYL-ALPHA-METHYLBENZYLAMINE(4108-58-1) information like chemical properties Structure melting point boiling point density molecular formula molecular weight physical properties toxicity information customs codes You can also browse global suppliers vendor prices Price manufacturers of (S)-(-)-N-BENZOYL-ALPHA

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aminum MoleculesGNU

aminum Molecules Structural Archive and Gallery 1H-Purine-2 6-dione 3 7-dihydro-1 3-dimethyl- compd with 1 2-ethanediamine (2:1) 3-AMINO-3-PICOLINE 317-34-0 Aminocardol Aminodur Aminophyllin Aminophylline Ammophyllin BY 108 Cardiofilina Cardiomin Cardophylin Cardophyllin Carena Cariomin DOBO Diaphylline Diophllin Diuxanthine Dura-Tab S M Aminophylline

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(S)

Visit ChemicalBook To find more (S)-(-)-N-BENZOYL-ALPHA-METHYLBENZYLAMINE(4108-58-1) information like chemical properties Structure melting point boiling point density molecular formula molecular weight physical properties toxicity information customs codes You can also browse global suppliers vendor prices Price manufacturers of (S)-(-)-N-BENZOYL-ALPHA

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(S)

Visit ChemicalBook To find more (S)-(-)-N-BENZOYL-ALPHA-METHYLBENZYLAMINE(4108-58-1) information like chemical properties Structure melting point boiling point density molecular formula molecular weight physical properties toxicity information customs codes You can also browse global suppliers vendor prices Price manufacturers of (S)-(-)-N-BENZOYL-ALPHA

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(S)

Visit ChemicalBook To find more (S)-(-)-N-BENZOYL-ALPHA-METHYLBENZYLAMINE(4108-58-1) information like chemical properties Structure melting point boiling point density molecular formula molecular weight physical properties toxicity information customs codes You can also browse global suppliers vendor prices Price manufacturers of (S)-(-)-N-BENZOYL-ALPHA

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(S)

Visit ChemicalBook To find more (S)-(-)-N-BENZOYL-ALPHA-METHYLBENZYLAMINE(4108-58-1) information like chemical properties Structure melting point boiling point density molecular formula molecular weight physical properties toxicity information customs codes You can also browse global suppliers vendor prices Price manufacturers of (S)-(-)-N-BENZOYL-ALPHA

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US3857889A

A general process for the isolation of an enantiomer present in excess in a partially resolved mixture of enantiomers of an organic compound which forms a racemic compound comprising treating the mixture with a crystallisation solvent and a solubilising agent whereby only the enantiomer present in excess passes into solution and is thereby separated from the insoluble

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