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144134

Sigma-Aldrich

3,5-Dimethylphenol

≥99%

Sinônimo(s):

5-Hydroxy-m-xylene, sym.-m-Xylenol

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About This Item

Fórmula linear:
(CH3)2C6H3OH
Número CAS:
108-68-9
Peso molecular:
122.16
Beilstein:
774117
Número CE:
203-606-5
Número MDL:
MFCD00002307
Código UNSPSC:
12352100
ID de substância PubChem:
24848632
NACRES:
NA.22

Nível de qualidade

100

Ensaio

≥99%

Formulário

fibers
solid

p.e.

222 °C (lit.)

pf

61-64 °C (lit.)
65-66 °C

cadeia de caracteres SMILES

Cc1cc(C)cc(O)c1

InChI

1S/C8H10O/c1-6-3-7(2)5-8(9)4-6/h3-5,9H,1-2H3

chave InChI

TUAMRELNJMMDMT-UHFFFAOYSA-N

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Aplicação

3,5-Dimethylphenol was used in simultaneous determination of urinary concentrations of phenol, o-, p-, m-cresols, 1-, 2-naphthol and xylenol isomers by capillary gas chromatography. It was used as starting reagent for total synthesis of landomycin A, most potent antitumor angucycline antibiotic and optically active polypropionate units.

Pictogramas

Skull and crossbonesCorrosion
GHS06,GHS05

Palavra indicadora

Danger

Frases de perigo

H301 + H311,H314

Classificações de perigo

Acute Tox. 3 Dermal - Acute Tox. 3 Oral - Eye Dam. 1 - Skin Corr. 1B

Código de classe de armazenamento

6.1A - Combustible acute toxic Cat. 1 and 2 / very toxic hazardous materials

Classe de risco de água (WGK)

WGK 2

Ponto de fulgor (°F)

179.6 °F

Ponto de fulgor (°C)

82 °C

Equipamento de proteção individual

Eyeshields, Faceshields, Gloves, type P3 (EN 143) respirator cartridges

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Certificados de análise (COA)

Lot/Batch Number
STBK1975
STBJ5333
STBJ3906
STBJ0460
STBH0695

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2,6-Dimethylphenol ≥99.5%

Sigma-Aldrich

D174904

2,6-Dimethylphenol

3,5-Dimethylbenzenethiol 90%

Sigma-Aldrich

522929

3,5-Dimethylbenzenethiol

Takashi Sugimura et al.
Organic letters, 6(24), 4439-4442 (2004-11-19)
Optically active polypropionate units were synthesized in 9-11 steps from 3,5-dimethylphenol. The sequence consists of the Buchner reaction controlled by a chiral 2,4-pentanediol tether and diastereoselective hydrogenation over Raney nickel. [reaction: see text]
Xiaoyu Yang et al.
Journal of the American Chemical Society, 133(32), 12433-12435 (2011-07-26)
The first total synthesis of landomycin A, the longest and most potent antitumor angucycline antibiotic, has been achieved in 63 steps and 0.34% overall yield starting from 2,5-dihydroxybenzoic acid, 3,5-dimethylphenol, triacetyl d-glucal, and d-xylose, with a convergent linear sequence of
S Laurent et al.
The quarterly journal of nuclear medicine and molecular imaging : official publication of the Italian Association of Nuclear Medicine (AIMN) [and] the International Association of Radiopharmacology (IAR), [and] Section of the Society of..., 53(6), 586-603 (2009-12-18)
Lanthanide complexes are more and more used in biomedical imaging as contrast agents (CA). The development of these paramagnetic complexes as CA for medical magnetic resonance imaging (MRI) and luminescent probes for optical imaging is very complementary. Gd complexes are
G Weibrich et al.
Bone, 34(4), 665-671 (2004-03-31)
This study analyzed the effect of the platelet count in platelet-rich plasma (PRP) on bone regeneration in vivo. Twenty male New Zealand white rabbits were used. PRP was produced using the Platelet Concentrate Collection System (PCCS) (3i, Miami, FL, USA).
M Yashiki et al.
Forensic science international, 47(1), 21-29 (1990-08-01)
A simple and rapid method for analysis of free and conjugated cresols in biological fluids was developed. Prior to and following freeing of the conjugated cresols by acid hydrolysis in a sealed ampoule, free cresols were extracted by Extrelut column
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