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Merck
CN

393851

2,6-二甲酰-4-甲基苯酚

97%

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线性分子式:
HOC6H2(CH3)(CHO)2
化学文摘社编号:
分子量:
164.16
NACRES:
NA.22
PubChem Substance ID:
UNSPSC Code:
12352100
EC Number:
230-768-4
MDL number:
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产品名称

2,6-二甲酰-4-甲基苯酚, 97%

InChI key

ZBOUXALQDLLARY-UHFFFAOYSA-N

InChI

1S/C9H8O3/c1-6-2-7(4-10)9(12)8(3-6)5-11/h2-5,12H,1H3

SMILES string

Cc1cc(C=O)c(O)c(C=O)c1

assay

97%

form

solid

mp

128-130 °C (lit.)

functional group

aldehyde

Quality Level

Application

2-Hydroxy-5-methyl-1,3-benzenedicarboxaldehyde (2-hydroxy-5-methylisophthalaldehyde) is suitable reagent used in the synthesis of 2-(2′-vinyloxyethoxy)-5-methylisophthaldehyde and chiral calixsalen macrocycles.
2-Hydroxy-5-methyl-1,3-benzenedicarboxaldehyde may be used in the synthesis of the following:
  • 3-[(2,4-Dichlorophenyl)iminomethyl]-2-hydroxy-5-methylbenzaldehyde, a Schiff base.
  • 2-Hydroxy-3-methoxymethyl-5-methylbenzaldehyde.
  • Acyclic Schiff-base ligands.
  • Macrobicyclic ligands (MSB).
  • 4-Methyl-2,6-divinylphenol.
  • 2-Hydroxy-3-dimethoxymethyl-5-methylbenzaldehyde.

General description

2-Hydroxy-5-methyl-1,3-benzenedicarboxaldehyde (2-hydroxy-5-methylisophthalaldehyde) is a dialdehyde derivative. It has been synthesized by heating p-cresol with hexamethylenetetramine. The structure has been confirmed by 1H and 13C NMR. It is an important raw material for the synthesis of various binucleating schiff base ligand.

pictograms

Exclamation mark

signalword

Warning

Hazard Classifications

Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

target_organs

Respiratory system

存储类别

11 - Combustible Solids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

dust mask type N95 (US), Eyeshields, Gloves


历史批次信息供参考:

分析证书(COA)

Lot/Batch Number

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3-[(2, 4-Dichlorophenyl) iminomethyl]-2-hydroxy-5-methylbenzaldehyde.
Kilic I, et al
Acta Crystallographica Section E, Structure Reports Online, 65(6), 1347-1347 (2009)
2-Hydroxy-3-methoxymethyl-5-methylbenzaldehyde.
Gunasekaran B, et al
Acta Crystallographica Section E, Structure Reports Online, 69(2), 317-317 (2013)
Steric effect in the free radical polymerization of vinyl ethers containing electron-deficient olefin groups.
Lee JY and Jin MK
Polymer Bull., 44(3), 2777-2284 (2000)
ESI MS, spectroscopic and semiempirical characterization of a macrobicyclic complex with Er (III) cation.
Przybylski P, et al.
Journal of Molecular Structure, 878(1), 95-103 (2008)
New efficient ruthenium metathesis catalyst containing chromenyl ligand.
Hryniewicka A, et al
Journal of Organometallic Chemistry, 695(9), 1265-1270 (2010)

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