140392

Sigma-Aldrich

4-Hydroxy-3,5-dimethylbenzaldehyde

95%

Synonym(s):
3,5-Dimethyl-4-hydroxybenzaldehyde
Linear Formula:
HOC6H2(CH3)2CHO
CAS Number:
Molecular Weight:
150.17
Beilstein/REAXYS Number:
1908717
EC Number:
MDL number:
PubChem Substance ID:
NACRES:
NA.22
Pricing and availability is not currently available.

Quality Level

assay

95%

mp

112-114 °C (lit.)

SMILES string

[H]C(=O)c1cc(C)c(O)c(C)c1

InChI

1S/C9H10O2/c1-6-3-8(5-10)4-7(2)9(6)11/h3-5,11H,1-2H3

InChI key

UYGBSRJODQHNLQ-UHFFFAOYSA-N

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Related Categories

Application

4-Hydroxy-3,5-dimethylbenzaldehydewas used as reagent during the phase transfer catalyzed polymerization of 4-hydroxy-3,5-dimethylbenzyl alcohol. It was used as starting reagent during the synthesis of 2,4,6-trimethylphenol.

Packaging

5 g in glass bottle

Pictograms

Exclamation mark

Signal Word

Warning

Hazard Statements

Precautionary Statements

Target Organs

Respiratory system

Personal Protective Equipment

dust mask type N95 (US),Eyeshields,Gloves

RIDADR

NONH for all modes of transport

WGK Germany

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

D J Abraham et al.
Biochemistry, 34(46), 15006-15020 (1995-11-21)
Monoaldehyde allosteric effectors of hemoglobin were designed, using molecular modeling software (GRID), to form a Schiff base adduct with the Val 1 alpha N-terminal nitrogens and interact via a salt bridge with Arg 141 alpha of the opposite subunit. The...
A facile synthesis of 4-alkoxymethylphenols by a copper (II)-acetoxime catalyst/O2 system.
Shimizu M, et al.
Tetrahedron Letters, 32(18), 2053-2056 (1991)
P R Ortiz de Montellano et al.
The Journal of biological chemistry, 262(24), 11641-11646 (1987-08-25)
Chloroperoxidase and H2O2 oxidize styrene to styrene oxide and phenylacetaldehyde but not benzaldehyde. The epoxide oxygen is shown by studies with H2(18)O2 to derive quantitatively from the peroxide. The epoxidation of trans-[1-2H]styrene by chloroperoxidase proceeds without detectable loss of stereochemistry...
Phase transfer catalyzed polymerization of 4-hydroxy-3, 5-dimethylbenzyl alcohol and copolymerization of 4-bromo-2, 6-dimethylphenol with 4-hydroxy-3, 5-dimethylbenzyl alcohol.
Wang JH and Percec V.
Polym. Bull., 25(1), 25-32 (1991)

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