1338073-34-9

Basic information

• Product Name: (S)-4,4,5,5-tetramethyl-2-(4-phenylbutan-2-yl)-1,3,2-dioxaborolane
• Synonyms: (S)-4,4,5,5-tetramethyl-2-(4-phenylbutan-2-yl)-1,3,2-dioxaborolane
• CAS NO: 1338073-34-9
• Molecular Weight: 260.184
• Mol File: 1338073-34-9.mol
• Article Data: 13

Chemical Properties

• CAS DataBase Reference: (S)-4,4,5,5-tetramethyl-2-(4-phenylbutan-2-yl)-1,3,2-dioxaborolane(CAS DataBase Reference)
• NIST Chemistry Reference: (S)-4,4,5,5-tetramethyl-2-(4-phenylbutan-2-yl)-1,3,2-dioxaborolane(1338073-34-9)
• EPA Substance Registry System: (S)-4,4,5,5-tetramethyl-2-(4-phenylbutan-2-yl)-1,3,2-dioxaborolane(1338073-34-9)

Safety Data

• Hazardous Substances Data: 1338073-34-9(Hazardous Substances Data)

Upstream product

• 94242-85-0 2,4,4,5,5-pentamethyl-[1,3,2]dioxaborolane 
• 218601-55-9 3-phenylpropyl N,N-diisopropylcarbamate 
• 34420-17-2 (2-phenylethyl)boronic acid 
• 76-09-5 2,3-dimethyl-2,3-butane diol 
• 165904-22-3 4,4,5,5-tetramethyl-2-phenethyl-1,3,2-dioxaborolane 
• 122-97-4 3-Phenyl-1-propanol 
• 1338073-31-6 3-phenylpropyl 2,4,6-triisopropylbenzoate 
• 768-56-9 4-Phenylbut-1-ene 
• 73183-34-3 bis(pinacol)diborane 
• 917-54-4 methyllithium 
• 104-53-0 3-phenyl-propionaldehyde 
• 1517-82-4 (1R,2S,5R,SS)-(-)-menthyl p-toluenesulfinate 
• 1391742-82-7 2-(4-phenylbut-1-en-2-yl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane 

Downstream Products

• 1338073-50-9 (R)-(3-iodobutyl)benzene 
• 2344-70-9 (+)-(S)-4-phenylbutan-2-ol 
• 1338073-53-2 (R)-diisopropyl 1-(4-phenylbutan-2-yl)hydrazine-1,2-dicarboxylate 
• 1338073-54-3 (R)-dibenzyl 1-(4-phenylbutan-2-yl)hydrazine-1,2-dicarboxylate 
• 1338073-56-5 (R)-7-(4-phenylbutan-2-yl)cyclohepta-1,3,5-triene 
• 1338073-55-4 (R)-2,2,6,6-tetramethyl-1-(4-phenylbutan-2-yloxy)piperidine 
• 2344-70-9 (R)-4-phenyl-2-butanol 

Relevant articles and documents

OPTICALLY ACTIVE 2,3-BISPHOSPHINOPYRAZINE DERIVATIVE, METHOD FOR PRODUCING SAME, TRANSITION METAL COMPLEX, AND METHOD FOR PRODUCING ORGANIC BORON COMPOUND

An optically active 2,3-bisphosphinopyrazine derivative represented by the following general formula (1): wherein R1 represents a group selected from a branched alkyl group having 3 or more carbon atoms, an adamantyl group, an optionally substi

Sterically Unprotected Nucleophilic Boron Cluster Reagents

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Synthesis of Secondary and Tertiary Alkyl Boronic Esters by gem-Carboborylation: Carbonyl Compounds as Bis(electrophile) Equivalents

An unprecedent gem-carboborylation of aldehydes and ketones provides access to various secondary and tertiary alkyl boronic esters. The addition of B2pin2 to a carbonyl compound generates α-oxyl-substituted alkyl boron species. Organ