EMBL-EBI | Chemical Biology | ChEBI

Example searches: iron*, InChI=1S/CH4O/c1-2/h2H,1H3, caffeine | Advanced Search

CHEBI:183312 - bis(pinacolato)diboron

ChEBI IDCHEBI:183312
ChEBI Namebis(pinacolato)diboron
Stars
DefinitionA 1,3,2-dioxaborolane that is 4,4,5,5-tetramethyl-1,3,2-dioxaborolane in which the boron hydrogen at position 2 is replaced by a 4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl group. It is a reagent used in organic synthesis to synthesise pinacol boronic esters.
Last Modified8 November 2021
SubmitterJohannes Hunold (ORCID: 0000-0002-4378-6061)
DownloadsMolfile
FormulaC12H24B2O4
Net Charge0
Average Mass253.944
Monoisotopic Mass254.18607
SMILESCC1(C)OB(B2OC(C)(C)C(C)(C)O2)OC1(C)C
InChIInChI=1S/C12H24B2O4/c1-9(2)10(3,4)16-13(15-9)14-17-11(5,6)12(7,8)18-14/h1-8H3
InChIKeyIPWKHHSGDUIRAH-UHFFFAOYSA-N
Wikipedia
Roles Classification
Biological Role:
EC 3.4.24.24 (gelatinase A) inhibitor  An EC 3.4.24.* (metalloendopeptidase) inhibitor that interferes with the action of gelatinase A (EC 3.4.24.24).
ChEBI Ontology
Outgoing Relation(s)
bis(pinacolato)diboron (CHEBI:183312) has role EC 3.4.24.24 (gelatinase A) inhibitor (CHEBI:84036)
bis(pinacolato)diboron (CHEBI:183312) is a 1,3,2-dioxaborolane (CHEBI:51636)
IUPAC Name 
4,4,4',4',5,5,5',5'-octamethyl-2,2'-bi-1,3,2-dioxaborolane
Synonyms  Source
octamethyl-2,2'-bi(1,3,2-dioxaborolane)ChEBI
bis(pinacolato)diboraneChemIDplus
B2pin2ChemIDplus
dipinacoldiboronChemIDplus
diboron pinacol esterChemIDplus
4,4,5,5-tetramethyl-2-(4,4,5,5-tetramethyl-1,3,2- dioxaborolan-2-yl)-1,3,2-dioxaborolaneIUPAC
Manual XrefsDatabases
Bis(pinacolato)diboronWikipedia
2015334ChemSpider
Registry NumbersSources
Reaxys:7703552Reaxys
CAS:73183-34-3ChemIDplus
Citations