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Merck
모든 사진(1)

주요 문서

393851

Sigma-Aldrich

2-Hydroxy-5-methyl-1,3-benzenedicarboxaldehyde

97%

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About This Item

Linear Formula:
HOC6H2(CH3)(CHO)2
CAS Number:
Molecular Weight:
164.16
EC Number:
MDL number:
UNSPSC 코드:
12352100
PubChem Substance ID:
NACRES:
NA.22

Quality Level

분석

97%

양식

solid

mp

128-130 °C (lit.)

작용기

aldehyde

SMILES string

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

InChI

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

InChI key

ZBOUXALQDLLARY-UHFFFAOYSA-N

일반 설명

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.[1] It is an important raw material for the synthesis of various binucleating schiff base ligand.[2]

애플리케이션

2-Hydroxy-5-methyl-1,3-benzenedicarboxaldehyde (2-hydroxy-5-methylisophthalaldehyde) is suitable reagent used in the synthesis of 2-(2′-vinyloxyethoxy)-5-methylisophthaldehyde[3] and chiral calixsalen macrocycles.[4]
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.[5]
  • 2-Hydroxy-3-methoxymethyl-5-methylbenzaldehyde.[6]
  • Acyclic Schiff-base ligands.[7]
  • Macrobicyclic ligands (MSB).[8]
  • 4-Methyl-2,6-divinylphenol.[1]
  • 2-Hydroxy-3-dimethoxymethyl-5-methylbenzaldehyde.[1]

픽토그램

Exclamation mark

신호어

Warning

유해 및 위험 성명서

Hazard Classifications

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

표적 기관

Respiratory system

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point (°F)

Not applicable

Flash Point (°C)

Not applicable

개인 보호 장비

dust mask type N95 (US), Eyeshields, Gloves


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문서 라이브러리 방문

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)
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)
2-Hydroxy-3-methoxymethyl-5-methylbenzaldehyde.
Gunasekaran B, et al
Acta Crystallographica Section E, Structure Reports Online, 69(2), 317-317 (2013)
Jian Gao et al.
Inorganic chemistry, 44(2), 232-241 (2005-01-18)
A family of novel chiral "calixsalen" Schiff base macrocycles R,R-H(3)L4, R,R-H(3)L5, containing three chiral diamino moieties were synthesized by an efficient self-assembly and characterized by (1)H and (13)C NMR, mass spectrometry, and X-ray diffraction. The systematic synthesis, structure, and coordination

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