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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/EA
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45-140414-25G 25 g
$63.30
1/EA
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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
Purity 99%
mp 59-61 °C (lit.)
UNSPSC 12352100

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