14366-96-2

Basic information

• Product Name: (2R*,3R*)-2-methyl-3-phenyl-1,3-butanediol
• CAS NO: 14366-96-2
• Molecular Weight: 180.247
• Mol File: 14366-96-2.mol
• Article Data: 7

Chemical Properties

• CAS DataBase Reference: (2R*,3R*)-2-methyl-3-phenyl-1,3-butanediol(CAS DataBase Reference)
• NIST Chemistry Reference: (2R*,3R*)-2-methyl-3-phenyl-1,3-butanediol(14366-96-2)
• EPA Substance Registry System: (2R*,3R*)-2-methyl-3-phenyl-1,3-butanediol(14366-96-2)

Safety Data

• Hazardous Substances Data: 14366-96-2(Hazardous Substances Data)

Upstream product

• 884497-15-8 (2R,3S)-methyl 3-hydroxy-2-methyl-3-phenylbutanoate 
• 54976-38-4 (E)-3-phenylbut-2-en-1-ol 
• 3393-64-4 4-hydroxy-3-methyl-2-butanone 
• 100-58-3 phenylmagnesium bromide 
• 191546-09-5 4-(tert-Butyl-dimethyl-silanyloxy)-3-methyl-butan-2-one 
• 16735-22-1 3-hydroxy-2-methylpropiophenone 
• 676-58-4 methylmagnesium chloride 
• 591-51-5 phenyllithium 
• 116047-21-3 3-((tert-butyl)dimethylsiloxy)-2-methyl-1-phenylpropan-1-one 
• 98-86-2 acetophenone 
• 108471-82-5 N,N,2-trimethyl-3-oxo-3-phenylpropanamide 
• 122489-20-7 (2R,3R,4Z)-3-methyl-2-phenyl-4-hexen-2-ol 
• 14664-76-7 methyl (Z)-2,3-dimethyl-3-phenyl-2-oxiranecarboxylate 
• 14366-98-4 (2RS,3SR) methyl 3-hydroxy-2-methyl-3-phenylbutanoate 

Downstream Products

• 85312-81-8 (2S^*,3R^*)-3-Hydroxy-2-methyl-3-phenylbutansaeure 
• 745813-71-2 (2S,3S)-toluenesulfonic acid 3-hydroxy-2-methyl-3-phenylbutyl ester 
• 745813-70-1 (2R,3S)-toluenesulfonic acid 3-hydroxy-2-methyl-3-phenylbutyl ester 

Relevant articles and documents

Stereoselective Addition of Organoaluminium or Organomanganese Reagents to 2-Methyl-3-oxo Amides (or Esters) Providing erythro or threo 2-Methyl-3-hydroxy Amides (or Esters)

Treatment of 2-methyl-3-oxo amides or 2-methyl-3-oxo esters with trialkylaluminium or alkylmanganese halide provided the corresponding erythro (or threo) 3-hydroxy-2-methyl amides or 3-hydroxy-2-methyl esters with high stereoselectivity.

Highly diastereo- and enantioselective copper-catalyzed domino reduction/aldol reaction of ketones with methyl acrylate

(Chemical Equation Presented) A good choice: A new catalytic method was found for the construction of stereogenic quaternary carbon centers through a copper-catalyzed domino conjugated reduction/aldol reaction of methyl acrylate with various alkyl aryl ke

Internal Lewis acid coordination as a powerful tool to promote highly stereoselective alkylation of α-alkyl-β-hydroxy ketones with Grignard reagents

An efficient and highly diastereoselective protocol is described for the alkylation of β-hydroxy ketones that contain an α-stereocenter. This method is based on the preliminary transformation of the β-hydroxy group into a titanium alcoholate by means of t