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M54201

Sigma-Aldrich

2-(Methylthio)aniline

97%

Synonym(s):

2-(Methylmercapto)aniline, 2-Aminothioanisole

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About This Item

Linear Formula:
CH3SC6H4NH2
CAS Number:
2987-53-3
Molecular Weight:
139.22
Beilstein/REAXYS Number:
386211
EC Number:
221-055-9
MDL number:
MFCD00007708
UNSPSC Code:
12352100
PubChem Substance ID:
24896998
NACRES:
NA.22

assay

97%

refractive index

n20/D 1.624 (lit.)

bp

234 °C (lit.)

density

1.111 g/mL at 25 °C (lit.)

SMILES string

CSc1ccccc1N

InChI

1S/C7H9NS/c1-9-7-5-3-2-4-6(7)8/h2-5H,8H2,1H3

InChI key

WBRPQQSADOCKCH-UHFFFAOYSA-N

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pictograms

Skull and crossbones
GHS06

signalword

Danger

hcodes

H301

Hazard Classifications

Acute Tox. 3 Oral

Storage Class

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

wgk_germany

WGK 3

flash_point_f

>235.4 °F - closed cup

flash_point_c

> 113 °C - closed cup

ppe

Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter

Certificates of Analysis (COA)

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Manisha Das et al.
Dalton transactions (Cambridge, England : 2003), 48(4), 1292-1313 (2019-01-05)
Rational ligand design approaches allowed {Cu2(μ-OH/OMe)} cores to be accommodated within μ-phenoxido bis(tetradentate) and μ-phenoxido bis(tridentate) ligands having thioether donors. The complexes [Cu2(μ-H2L1)(μ-OH)](ClO4)2·2H2O (1), [Cu2(μ-L2)(μ-OH)(OH2)](ClO4)2 (2a) and [Cu2(μ-L2)(μ-OCH3)(OH2)](ClO4)2 (2b) were obtained from an N2O3S2 donor set bearing the H3L1 ligand
Takashi Ikawa et al.
Chemistry (Weinheim an der Bergstrasse, Germany), 26(19), 4320-4332 (2020-01-03)
Benzynes were selectively generated in situ from phenols and trapped regioselectively with potassium hexamethyldisilazide to form primary anilines following acidic workup. The direct conversion of a phenolic hydroxyl group into a free amino group is a useful method for the

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