4-tert-Butyl-2,6-diformylphenol

Names

[ Name ]:
4-tert-Butyl-2,6-diformylphenol

[Synonym ]:
5-tert-butyl-2-hydroxybenzene-1,3-dicarbaldehyde
2-Hydroxy-5-(2-methyl-2-propanyl)isophthalaldehyde
MFCD01567135
1,3-Benzenedicarboxaldehyde, 5-(1,1-dimethylethyl)-2-hydroxy-

Chemical & Physical Properties

[ Density]:
1.2±0.1 g/cm3

[ Boiling Point ]:
267.8±40.0 °C at 760 mmHg

[ Melting Point ]:
99-103ºC(lit.)

[ Molecular Formula ]:
C₁₂H₁₄O₃

[ Molecular Weight ]:
206.238

[ Flash Point ]:
130.0±23.8 °C

[ Exact Mass ]:
206.094299

[ PSA ]:
54.37000

[ LogP ]:
3.70

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

[ Index of Refraction ]:
1.590

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 ]:
36/37/38

[ Safety Phrases ]:
26-36

[ RIDADR ]:
NONH for all modes of transport

[ HS Code ]:
2912499000

Synthetic Route

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Precursor & DownStream

Precursor

DownStream

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

The first example of erbium triple-stranded helicates displaying SMM behaviour.

Dalton Trans. 44(38) , 16833-9, (2015)

A series of isostructural C3-symmetrical triple stranded dinuclear lanthanide [Ln2L3](NO3)3 molecules have been synthesized using subcomponent self-assembly of Ln(NO3)3 with 2-(methylhydrazino)benzimi...

Binuclear and polynuclear transition metal complexes with macrocyclic ligands. 2. New macrocyclic Schiff" s base in the reaction of 4-tert-butyl-2, 6-diformylphenol with 1, 2-diaminobenzene. Synthesis and structural, spectroscopic, and theoretical study. Ustynyuk YA, et al.

Russ. Chem. Bull. 51(3) , 488-498, (2002)

Mono-and diformylation of 4-substituted phenols: a new application of the Duff reaction. Lindoy LF, et al.

Synthesis 07 , 1029-1032, (1998)