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

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

CAS No.:
37942-07-7
Catalog Number:
AG003IPN
Molecular Formula:
C15H22O2
Molecular Weight:
234.3340
Pack Size
Purity
Availability
Location
Price(USD)
Quantity
  
10g
95%
In Stock USA
United States
$13
- +
25g
95%
In Stock USA
United States
$18
- +
100g
95%
In Stock USA
United States
$63
- +
500g
95%
In Stock USA
United States
$188
- +
Product Description
Catalog Number:
AG003IPN
Chemical Name:
3,5-Di-tert-butyl-2-hydroxybenzaldehyde
CAS Number:
37942-07-7
Molecular Formula:
C15H22O2
Molecular Weight:
234.3340
MDL Number:
MFCD00191998
IUPAC Name:
3,5-ditert-butyl-2-hydroxybenzaldehyde
InChI:
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
SMILES:
O=Cc1cc(cc(c1O)C(C)(C)C)C(C)(C)C
EC Number:
629-676-0
Properties
Complexity:
270  
Compound Is Canonicalized:
Yes
Covalently-Bonded Unit Count:
1  
Defined Atom Stereocenter Count:
0
Defined Bond Stereocenter Count:
0
Exact Mass:
234.162g/mol
Formal Charge:
0
Heavy Atom Count:
17  
Hydrogen Bond Acceptor Count:
2  
Hydrogen Bond Donor Count:
1  
Isotope Atom Count:
0
Molecular Weight:
234.339g/mol
Monoisotopic Mass:
234.162g/mol
Rotatable Bond Count:
3  
Topological Polar Surface Area:
37.3A^2
Undefined Atom Stereocenter Count:
0
Undefined Bond Stereocenter Count:
0
XLogP3:
4.9  
Literature
Title Journal
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Highly selective fluorescent chemosensor for Zn2+ derived from inorganic-organic hybrid magnetic core/shell Fe3O4@SiO2 nanoparticles. Nanoscale research letters 20120101
Unsymmetric salen ligands bearing a Lewis base: intramolecularly cooperative catalysis for cyanosilylation of aldehydes. Organic & biomolecular chemistry 20110921
Solid phase extraction of copper(II) ions using C18-silica disks modified by oxime ligands. Journal of hazardous materials 20100715
Soluble monometallic salen complexes derived from O-functionalised diamines as metalloligands for the synthesis of heterobimetallic complexes. Dalton transactions (Cambridge, England : 2003) 20100507
6,8-Di-tert-butyl-3-(4-nitro-phen-yl)-2H-chromen-2-one. Acta crystallographica. Section E, Structure reports online 20100201
2,4-Di-tert-butyl-6-[(2,5-difluorophenyl)iminomethyl]phenol. Acta crystallographica. Section E, Structure reports online 20091101
Trinuclear C3-symmetric extension of Jacobsen's catalyst: synthesis, characterization, and catalytic properties of a chiral trinuclear Mn(III) triplesalen complex. Inorganic chemistry 20091005
Copper(II) complexes of thioether-substituted salcyen and salcyan derivatives and their silver(I) adducts. Dalton transactions (Cambridge, England : 2003) 20051007
Vanadium-catalyzed asymmetric oxidation of alpha-hydroxy esters using molecular oxygen as stoichiometric oxidant. Journal of the American Chemical Society 20050202
Synthesis, spectroscopy, and electrochemistry of copper(II) complexes with N,N'-bis(3,5-di-t-butylsalicylideneimine)polymethylenediamine ligands. Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy 20050101
Boron-nitrogen macrocycles: a new generation of calix[3]arenes. Chemical communications (Cambridge, England) 20041221
Spectroscopic and electrochemical characterization of di-tert-butylated sterically hindered Schiff bases and their phenoxyl radicals. Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy 20041101
Enantioselective synthesis of DIANANE, a novel C2-symmetric chiral diamine for asymmetric catalysis. The Journal of organic chemistry 20040430
Catalytic, asymmetric synthesis of cyanohydrin ethyl carbonates. Organic letters 20031113
Properties