3,5-Di-tert-butyl-2-hydroxybenzaldehyde

ALDRICH/140414 - 99%

Synonym: 3,5-Di-tert-butylsalicylaldehyde

CAS Number: 37942-07-7
Empirical Formula (Hill Notation): C₁₅H₂₂O₂
Molecular Weight: 234.33
MDL Number: MFCD00191998
Linear Formula: HOC₆H₂[C(CH₃)₃]₂CHO
Product Type: Chemical

Catalog Number	PKG Qty.	Price	Quantity


45-140414-5G	5 g	$52.30 1/EAAdd To Favorites		Add To Favorites
45-140414-25G	25 g	$63.30 1/EAAdd To Favorites		Add To Favorites

assay	99%
form	powder or crystals
functional group	aldehyde
InChI	1S/C15H22O2/c1-14(2,3)11-7-10(9-16)13(17)12(8-11)15(4,5)6/h7-9,17H,1-6H3
InChI key	RRIQVLZDOZPJTH-UHFFFAOYSA-N
mp	59-61 °C (lit.)
Quality Level	100
SMILES string	CC(C)(C)c1cc(C=O)c(O)c(c1)C(C)(C)C

Application:	3,5-Di-tert-butyl-2-hydroxybenzaldehyde was used in the synthesis of • Mn(III)-salen complex and its diamino precursor 5,6-diamino-5,6-dideoxy-1,2-O-isopropylidene-3-O-methyl-β-L-idofuranose • chiral Schiff base ligand for an enantioselective copper-catalyzed addition of phenylacetylene to imines • chiral oxazolidine ligand for the enantioselective addition of diethylzinc to aldehydes • tin Schiff base complexes with histidine analogues
General description:	3,5-Di-tert-butyl-2-hydroxybenzaldehyde undergoes condensation reaction with • methyl-2-{N-(2′-aminoethane)}-amino-1-cyclopentenedithiocarboxylate to yield Schiff base ligand • N,N-diethyl-2-methyl-1,4-phenylenediamine during the synthesis of copper(II) and cobalt(II) complexes of salicylaldimine
Packaging:	25 g in poly bottle
Packaging:	5 g in glass bottle