174004-13-8

Basic information

• Product Name: (R)-1-aza-2-bora-2-((triMethylsilyl)Methyl)-3-oxa-4,4-diphenylbicyclooctane
• Synonyms: (R)-1-aza-2-bora-2-((triMethylsilyl)Methyl)-3-oxa-4,4-diphenylbicyclooctane;1H,3H-Pyrrolo[1,2-c][1,3,2]oxazaborole, tetrahydro-3,3-diphenyl-1-[(triMethylsilyl)Methyl]-, (3aS)-;(S)-3,3-Diphenyl-1-[trimethylsilylmethyl]tetrahydro-1H,3H-pyrrolo[1,2-c][1,3,2]oxazaborole
• CAS NO: 174004-13-8
• Molecular Formula: C21H28BNOSi
• Molecular Weight: 349.34962
• Mol File: 174004-13-8.mol
• Article Data: 0

Chemical Properties

• Appearance: /
• CAS DataBase Reference: (R)-1-aza-2-bora-2-((triMethylsilyl)Methyl)-3-oxa-4,4-diphenylbicyclooctane(CAS DataBase Reference)
• NIST Chemistry Reference: (R)-1-aza-2-bora-2-((triMethylsilyl)Methyl)-3-oxa-4,4-diphenylbicyclooctane(174004-13-8)
• EPA Substance Registry System: (R)-1-aza-2-bora-2-((triMethylsilyl)Methyl)-3-oxa-4,4-diphenylbicyclooctane(174004-13-8)

Safety Data

• Hazardous Substances Data: 174004-13-8(Hazardous Substances Data)

Usage

General Description

This chemical, commonly referred to as TIPS-CH2BPin, is a boron-containing compound with a unique structure that includes a tetrahydropyrrolo[1,2-c][1,3,2]oxaborole group. It is widely used as a reagent in organic synthesis, particularly in the formation of carbon-carbon bonds and the functionalization of organic molecules. TIPS-CH2BPin is known for its ability to facilitate a variety of important reactions, such as the Suzuki-Miyaura cross-coupling and the hydroboration of alkenes. Its trimethylsilyl group makes it a highly versatile and stable reagent, and its boron center enables it to participate in a range of catalytic processes. [(3aS)-3,3-diphenyl-3a,4,5,6-tetrahydropyrrolo[1,2-c][1,3,2]oxazaborol-1-yl]methyl-trimethylsilane has applications in pharmaceutical, agrochemical, and materials science research, and its unique structure and reactivity continue to make it an important tool for synthetic chemists.