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Merck

T28525

Sigma-Aldrich

4-Methylbenzenethiol

98%

Sinónimos:

p-Thiocresol, 4-Mercaptotoluene, 4-Methylthiophenol, p-Toluenethiol, p-Tolyl mercaptan

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About This Item

Fórmula lineal:
CH3C6H4SH
Número de CAS:
Peso molecular:
124.20
Beilstein/REAXYS Number:
605761
EC Number:
MDL number:
UNSPSC Code:
12162002
PubChem Substance ID:
NACRES:
NA.23

vapor density

6.2 (vs air)

Quality Level

vapor pressure

10 mmHg ( 71 °C)

assay

98%

bp

195 °C (lit.)

mp

41-43 °C (lit.)

SMILES string

Cc1ccc(S)cc1

InChI

1S/C7H8S/c1-6-2-4-7(8)5-3-6/h2-5,8H,1H3

InChI key

WLHCBQAPPJAULW-UHFFFAOYSA-N

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pictograms

Exclamation mark

signalword

Warning

hcodes

Hazard Classifications

Eye Irrit. 2

Storage Class

11 - Combustible Solids

wgk_germany

WGK 3

flash_point_f

154.4 °F - closed cup

flash_point_c

68 °C - closed cup

ppe

Eyeshields, Gloves, type N95 (US)


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Organosulfur compounds show cytotoxic potential towards many tumor cell lines. Disulfides and thiosulfonates act through apoptotic processes, inducing proteins associated with apoptosis, endoplasmic reticulum stress, and the unfolded protein response. Three p-substituted symmetric diaryl disulfides and three diaryl thiosulfonates were
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Fabrication of large-area devices with patternable nanostructures is important for practical applications in optical or electrical devices. In this work, we describe an easy and environment-friendly method for preparing large-area nano-dot (ND) arrays via the electrolytic reaction of a metal
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Hay synthesis of a novel series of symmetrically tetra-substituted thiophenyl zinc(II)phthalocyanines (RS)4ZnPcs 4a-c was reported. Their novel 4-thiophenyl-phthalonitriles precursors 3(a-c) were synthesized from their substituted thiophenols 2(a-c). They were screened for their in-vitro antitumor activity on Human lung adenocarcinoma (A549)

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