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

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Names

[ CAS No. ]:
37942-07-7

[ Name ]:
3,5-Di-tert-butyl-2-hydroxybenzaldehyde

[Synonym ]:
MFCD00191998
3,5-di-tert-butyl-2-hydroxybenzaldehyde
3,5-di-tert-Butyl Salicylaldehyde
3,5-Di-tert-butyl-2-hydroxybenzolcarbaldehyd
3,5-Di-tert-butylsalicylaldehyde
3,5-Bis(1,1-Dimethylethyl)-2-Hydroxy-Benzaldehyde
Benzaldehyde, 3,5-bis(1,1-dimethylethyl)-2-hydroxy-
3,5-ditert-butyl-2-hydroxybenzaldehyde
2-Hydroxy-3,5-bis(2-methyl-2-propanyl)benzaldehyde

Chemical & Physical Properties

[ Density]:
1.0±0.1 g/cm3

[ Boiling Point ]:
277.6±35.0 °C at 760 mmHg

[ Melting Point ]:
59-61 °C(lit.)

[ Molecular Formula ]:
C15H22O2

[ Molecular Weight ]:
234.334

[ Flash Point ]:
116.1±18.5 °C

[ Exact Mass ]:
234.161987

[ PSA ]:
37.30000

[ LogP ]:
4.98

[ Vapour Pressure ]:
0.0±0.6 mmHg at 25°C

[ Index of Refraction ]:
1.528

MSDS

Click to get detail MSDS

Safety Information

[ Symbol ]:

GHS07

[ Signal Word ]:
Warning

[ Hazard Statements ]:
H315-H319-H335

[ Precautionary Statements ]:
P261-P305 + P351 + P338

[ Personal Protective Equipment ]:
dust mask type N95 (US);Eyeshields;Gloves

[ Hazard Codes ]:
Xi: Irritant;

[ Risk Phrases ]:
R36/37/38

[ Safety Phrases ]:
S26-S36

[ RIDADR ]:
NONH for all modes of transport

[ WGK Germany ]:
3

[ HS Code ]:
2912499000

Synthetic Route

Click to get detail synthetic route

Precursor & DownStream

Precursor

  • Formaldehyde
  • 2,4-Di-t-butylphenol
  • 2,4-ditert-butyl-6-(hydroxymethyl)phenol
  • 2-(dimethylaminomethyl)-4,6-ditert-butyl-phenol
  • Phenol
  • Methanol
  • 2,4-Di-tert-butyl-6-methylphenol
  • 2,4-DIISOPROPYLPHENOL
  • Aminoform

DownStream

  • 2,4-ditert-butyl-6-(methylaminomethylidene)cyclohexa-2,4-dien-1-one
  • 2,4-ditert-butyl-6-[(pyridin-2-ylmethylamino)methyl]phenol
  • 2,4-ditert-butyl-6-[(4-methylanilino)methylidene]cyclohexa-2,4-dien-1-one
  • 2,4-ditert-butyl-6-[(2-methoxyanilino)methylidene]cyclohexa-2,4-dien-1-one
  • 3,5-DI-TERT-BUTYL-2-METHOXYBENZALDEHYDE
  • 2,4-ditert-butyl-6-[(2-hydroxyanilino)methylidene]cyclohexa-2,4-dien-1-one
  • 2,4-ditert-butyl-6-[(propan-2-ylamino)methylidene]cyclohexa-2,4-dien-1-one
  • (R,R)-(-)-N,N'-Bis(3,5-di-tert-butylsalicylidene)-1,2-cyclohexanediamine
  • (S,S)-(+)-N,N'-Bis(3,5-di-tert-butylsalicylidene)-1,2-cyclohexanediamine
  • (S)-(-)-2-(3 5-DI-TERT-BUTYLSALICYLIDEN&

Customs

[ HS Code ]: 2912499000

[ Summary ]:
2912499000. other aldehyde-ethers, aldehyde-phenols and aldehydes with other oxygen function. VAT:17.0%. Tax rebate rate:9.0%. . MFN tariff:5.5%. General tariff:30.0%

Articles

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.

Spectrochim. Acta. A. Mol. Biomol. Spectrosc. 97 , 1033-40, (2012)

A novel Schiff base (H(2)cddi(t)butsalen) ligand was prepared via condensation of Methyl-2-{N-(2'-aminoethane)}-amino-1-cyclopentenedithiocarboxylate(Hcden) and 3,5-di-tert-butyl-2-hydroxybenzaldehyde...

Novel Organotin(IV) Schiff Base Complexes with Histidine Derivatives: Synthesis, Characterization, and Biological Activity.

Bioinorg. Chem. Appl. 2013 , 502713, (2013)

Five novel tin Schiff base complexes with histidine analogues (derived from the condensation reaction between L-histidine and 3,5-di-tert-butyl-2-hydroxybenzaldehyde) have been synthesized and charact...

Tetrahedron Asymmetry 18 , 1124, (2007)


More Articles

Related Compounds

  • (3,5-di-tert-butyl-2-oxo-2,3-dihydro-2λ5-[1,3,2]oxazaphosphol-2-yl)-dimethyl-amine
  • 3,5-di-tert-butyl-2-hydroxybenzamide
  • 3,5-di-tert-butyl-2-chloro-Δ4-1,3,2-oxazaphospholine 2-oxide
  • (3,5-di-tert-butyl-2-methoxyphenyl)boronic acid
  • 3,5-di-tert-butyl-2-methoxyaniline
  • 3,5-di-tert-butyl-2-chloroaniline
  • {1-[4-Fluoro-2-(trifluoromethyl)phenyl]cyclobutyl}methanol
  • 2-(5-Bromo-2-cyclopropylpyrimidin-4-yl)-2-oxoacetic acid
  • 2-(1-Bromopropan-2-yl)-1,3-difluoro-4-methylbenzene
  • 1-Amino-3-[2-(dimethylamino)-4-methyl-1,3-thiazol-5-yl]propan-2-ol
  • 4-(2-Amino-3,3,3-trifluoropropyl)-2-bromophenol
  • rac-[(1R,2R)-2-(1-methyl-1H-imidazol-4-yl)cyclopropyl]methanamine
  • 3-(Aminomethyl)-3-(5-methylpyridin-3-yl)cyclobutan-1-ol
  • 1-Amino-2-[5-fluoro-2-(trifluoromethyl)phenyl]propan-2-ol
  • 1-[3-(4-fluorophenyl)-1H-pyrazol-4-yl]cyclopropan-1-ol
  • 2-(5-Bromo-3-methylfuran-2-yl)-1-methylpiperazine
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