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302589

Sigma-Aldrich

2-Methylresorcinol

98%

Sinonimo/i:

2,6-Dihydroxytoluene

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About This Item

Formula condensata:
CH3C6H3(OH)2
Numero CAS:
608-25-3
Peso molecolare:
124.14
Beilstein:
2042177
Numero CE:
210-155-8
Numero MDL:
MFCD00002271
Codice UNSPSC:
12352100
ID PubChem:
24858264
NACRES:
NA.22

Livello qualitativo

100

Saggio

98%

Stato

solid

P. ebollizione

264 °C (lit.)

Punto di fusione

114-120 °C (lit.)

Stringa SMILE

Cc1c(O)cccc1O

InChI

1S/C7H8O2/c1-5-6(8)3-2-4-7(5)9/h2-4,8-9H,1H3
ZTMADXFOCUXMJE-UHFFFAOYSA-N

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Descrizione generale

The reaction between 2-methylresorcinol and 2-alkenals was studied to investigate the scavenging ability of m-diphenols for the 2-alkenals formed during lipid oxidation.

Applicazioni

2-Methylresorcinol was used in the synthesis of:
  • C-5-bromo-2-hydroxyphenylcalix[4]-2-methylresorcinarene
  • tripyrrane analogs
  • series of novel aromatic benziporphyrins

Avvertenze

Danger

Indicazioni di pericolo

H301,H317,H318,H400

Classi di pericolo

Acute Tox. 3 Oral - Aquatic Acute 1 - Eye Dam. 1 - Skin Sens. 1B

Codice della classe di stoccaggio

6.1C - Combustible acute toxic Cat.3 / toxic compounds or compounds which causing chronic effects

Classe di pericolosità dell'acqua (WGK)

WGK 3

Punto d’infiammabilità (°F)

275.0 °F - closed cup

Punto d’infiammabilità (°C)

135 °C - closed cup

Dispositivi di protezione individuale

Eyeshields, Faceshields, Gloves, type P2 (EN 143) respirator cartridges

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Certificati d'analisi (COA)

Lot/Batch Number
MKCP2185
MKCL4757
MKCL1622
MKCG2614
MKCD0057

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Sigma-Aldrich

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Sigma-Aldrich

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Sigma-Aldrich

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Sigma-Aldrich

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Sigma-Aldrich

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Kae Miyake et al.
Chemical communications (Cambridge, England), (2)(2), 178-179 (2004-01-23)
Acid catalyzed condensation of resorcinol or 2-methylresorcinol with 2 equiv. of an acetoxymethylpyrrole gave bis(pyrrolylmethyl)benzene derivatives in moderate yields; these afforded a series of novel aromatic benziporphyrins using the MacDonald "3 + 1" methodology.
Hamza M Abosadiya et al.
Molecules (Basel, Switzerland), 18(11), 13369-13384 (2013-11-01)
C-5-bromo-2-hydroxyphenylcalix[4]-2-methylresorcinarene (I) was synthesized by cyclocondensation of 5-bromo-2-hydroxybenzaldehyde and 2-methylresorcinol in the presence of concentrated HCl. Compound I was characterized by infrared and nuclear magnetic resonance spectroscopic data. X-ray analysis showed that this compound crystallized in a triclinic system with
Francisco J Hidalgo et al.
Food chemistry, 160, 118-126 (2014-05-07)
The reaction between m-diphenols (resorcinol, 2-methylresorcinol, 2,5-dimethylresorcinol, 3-methylphenol, orcinol, and phloroglucinol) and 2-alkenals (2-pentenal and 2-octenal) was studied in an attempt to understand the chemical pathways involved in the scavenging ability of m-diphenols for the 2-alkenals produced as a consequence
Timothy D Lash et al.
The Journal of organic chemistry, 76(15), 6295-6308 (2011-06-23)
Tripyrrane analogues were prepared by reacting resorcinol or 2-methylresorcinol with 2 equiv of an acetoxymethylpyrrole in the presence of p-toluenesulfonic acid and calcium chloride. Following removal of the benzyl ester protective groups, the resorcinol-derived benzitripyrrane was reacted with a pyrrole
Hye Jung Choi et al.
Journal of microbiology and biotechnology, 22(9), 1214-1217 (2012-07-21)
One Helicosporium strain, isolated from a wilted chestnut tree, evidenced in vitro antimicrobial activity against various types of bacteria and fungi, and generated a diffusible pigment. The antimicrobial compounds and the diffusible pigment of the Helicosporium sp. isolate were purified
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Protocolli

HPLC Analysis of Catechols and Resorcinols on Ascentis® RP-Amide

Separation of Resorcinol 50 mg/mL; Pyrocatechol; 2-Methylresorcinol; 4-Methylcatechol; 2,5-Dimethylresorcinol 50 mg/mL; 3-Methylcatechol 50 mg/mL; 4-Nitrocatechol 50 mg/mL

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