Home Aldehydes 37942-07-7
37942-07-7,MFCD00191998
Catalog No.:AA003IMV
37942-07-7 | 3,5-Di-tert-butyl-2-hydroxybenzaldehyde
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5g
97+%
in stock  
$12.00   $8.00
- +
10g
95%
in stock  
$15.00   $10.00
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25g
97+%
in stock  
$18.00   $12.00
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100g
97+%
in stock  
$60.00   $42.00
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500g
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$125.00   $87.00
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  • Technical Information
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Technical Information
Catalog Number:
AA003IMV
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
Computed 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  

Synonyms
 
3,5-Di-tert-butyl-2-hydroxybenzaldehyde 
37942-07-7 
3,5-Di-tert-butylsalicaldehyde, 99% 
3,5-bis(tert-butyl)-2-hydroxybenzaldehyde 
PubChem11247 
3,5-di-ter-butyl-2-hydroxybenzylaldehyde 
ACMC-1AETE 
AC1LEL5W 
AC1Q1LVL 
KSC490M0J 
SCHEMBL187267 
BEN057 
3,5-Di-tert-butylsalicylaldehyde 
CHEMBL427197 
3,5-Ditert-butylsalicylaldehyde 
Jsp006677 
CTK3J0604 
ZINC56444 
DTXSID80350777 
3,5-di-tert-butyl salicylaldehyde 
3,5-Bis(tert-butyl)salicylaldehyde 
ACT07884 
ANW-28761 
3,5-Bis(1,1-dimethylethyl)-2-hydroxy-benzaldehyde 
SBB052181 
STK744365 
3,5-di-t-butyl-2-hydroxybenzaldehyde 
AKOS000113415 
CS-W012904 
LS10589 
MCULE-1344879502 
PS-7663 
RP28130 
RP28131 
Benzaldehyde, 3,5-bis(1,1-dimethylethyl)-2-hydroxy- 
RTR-036642 
2-hydroxy-3,5-ditert.butylbenzaldehyde 
3,5-ditert-butyl-2-hydroxybenzaldehyde 
KS-0000020A 
3,5-ditert-butyl-2-hydroxy-benzaldehyde 
NCGC00328863-01 
AC-11236 
AJ-09264 
AK-50558 
BR-50558 
3,5-Di-t-butylsalicylaldehyde 
CJ-00348 
O338 
SY014855 
ZB001647 
3,5-di-tert-butyl-2-hydroxy benzaldehyde 
3,5-di-tert.-butyl-2-hydroxybenzaldehyde 
AB0016399 
DB-022117 
ST2410279 
TL8002784 
RRIQVLZDOZPJTH-UHFFFAOYSA-N 
TR-036642 
A6448 
AM20050219 
D2646 
FT-0614729 
FT-0614730 
ST50825840 
MFCD00191998 (98%) 
3,5-Di-tert-butyl-2-hydroxybenzaldehyde, 99% 
M-1776 
MFCD00191998 
AB01322446-02 
942D077 
I01-2090 
W-202554 
InChI=1/C15H22O2/c1-14(2,3)11-7-10(9-16)13(17)12(8-11)15(4,5)6/h7-9,17H,1-6H 
C15H22O2 
CID688023 
ZINC00056444 
3,5-Di-tert-butyl-4-hydroxybenzaldehyde 
3,5-Di-tert-butyl-2-hydroxybenzaldehyde, 99% 5g 
3,5-Di-tert-butyl-2-hydroxy-benzaldehyde 
3,5-Di-tert-butyl-2-hydroxybenzaldehyde, 99% - 100G 100g 
1620-98-0 
Benzaldehyde, 2-hydroxy, 3,5-di(t-butyl) 
Literature

Title: Synthesis, characterization and electrochemical study of synthesis of a new Schiff base (H₂cddi(t)butsalen) ligand and their two asymmetric Schiff base complexes of Ni(II) and Cu(II) with NN'OS coordination spheres.

Journal: Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy 20121101

Title: Highly selective fluorescent chemosensor for Zn2+ derived from inorganic-organic hybrid magnetic core/shell Fe3O4@SiO2 nanoparticles.

Journal: Nanoscale research letters 20120101

Title: Unsymmetric salen ligands bearing a Lewis base: intramolecularly cooperative catalysis for cyanosilylation of aldehydes.

Journal: Organic & biomolecular chemistry 20110921

Title: Solid phase extraction of copper(II) ions using C18-silica disks modified by oxime ligands.

Journal: Journal of hazardous materials 20100715

Title: Soluble monometallic salen complexes derived from O-functionalised diamines as metalloligands for the synthesis of heterobimetallic complexes.

Journal: Dalton transactions (Cambridge, England : 2003) 20100507

Title: 6,8-Di-tert-butyl-3-(4-nitro-phen-yl)-2H-chromen-2-one.

Journal: Acta crystallographica. Section E, Structure reports online 20100201

Title: 2,4-Di-tert-butyl-6-[(2,5-difluorophenyl)iminomethyl]phenol.

Journal: Acta crystallographica. Section E, Structure reports online 20091101

Title: Trinuclear C3-symmetric extension of Jacobsen's catalyst: synthesis, characterization, and catalytic properties of a chiral trinuclear Mn(III) triplesalen complex.

Journal: Inorganic chemistry 20091005

Title: Copper(II) complexes of thioether-substituted salcyen and salcyan derivatives and their silver(I) adducts.

Journal: Dalton transactions (Cambridge, England : 2003) 20051007

Title: Vanadium-catalyzed asymmetric oxidation of alpha-hydroxy esters using molecular oxygen as stoichiometric oxidant.

Journal: Journal of the American Chemical Society 20050202

Title: Synthesis, spectroscopy, and electrochemistry of copper(II) complexes with N,N'-bis(3,5-di-t-butylsalicylideneimine)polymethylenediamine ligands.

Journal: Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy 20050101

Title: Boron-nitrogen macrocycles: a new generation of calix[3]arenes.

Journal: Chemical communications (Cambridge, England) 20041221

Title: Spectroscopic and electrochemical characterization of di-tert-butylated sterically hindered Schiff bases and their phenoxyl radicals.

Journal: Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy 20041101

Title: Enantioselective synthesis of DIANANE, a novel C2-symmetric chiral diamine for asymmetric catalysis.

Journal: The Journal of organic chemistry 20040430

Title: Catalytic, asymmetric synthesis of cyanohydrin ethyl carbonates.

Journal: Organic letters 20031113

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