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155705

3-Methoxythiophenol

98%

Synonym(s):

3-Mercaptoanisole, 3-Methoxybenzenethiol

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About This Item

Linear Formula:
CH3OC6H4SH
CAS Number:
15570-12-4
Molecular Weight:
140.20
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
24849559
EC Number:
239-617-7
Beilstein/REAXYS Number:
2041496
MDL number:
MFCD00004841
Assay:
98%
Form:
liquid

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InChI key

QMVAZEHZOPDGHA-UHFFFAOYSA-N

InChI

1S/C7H8OS/c1-8-6-3-2-4-7(9)5-6/h2-5,9H,1H3

SMILES string

COc1cccc(S)c1

assay

98%

form

liquid

refractive index

n20/D 1.587 (lit.)

bp

223-226 °C (lit.)

density

1.13 g/mL at 25 °C (lit.)

storage temp.

2-8°C

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This Item
184055277681591653
3-Methoxythiophenol 98%

Sigma-Aldrich

155705

3-Methoxythiophenol

2-Methoxythiophenol 97%

Sigma-Aldrich

184055

2-Methoxythiophenol

3-Methyl-3-oxetanemethanol 98%

Sigma-Aldrich

277681

3-Methyl-3-oxetanemethanol

Methyl (3S)-(+)-3-(methyl-1H-indol-3-yl)-3-phenylpropionate 98%

Sigma-Aldrich

591653

Methyl (3S)-(+)-3-(methyl-1H-indol-3-yl)-3-phenylpropionate

assay

98%

assay

97%

assay

98%

assay

98%

bp

223-226 °C (lit.)

bp

99 °C/8 mmHg (lit.)

bp

80 °C/40 mmHg (lit.)

bp

-

density

1.13 g/mL at 25 °C (lit.)

density

1.152 g/mL at 25 °C (lit.)

density

1.024 g/mL at 25 °C (lit.)

density

-

refractive index

n20/D 1.587 (lit.)

refractive index

n20/D 1.591 (lit.)

refractive index

n20/D 1.446 (lit.)

refractive index

-

storage temp.

2-8°C

storage temp.

-

storage temp.

2-8°C

storage temp.

-

form

liquid

form

liquid

form

liquid

form

solid

Application

3-Methoxythiophenol was used in the preparation of allenes.

pictograms

Exclamation mark
GHS07

signalword

Warning

Hazard Classifications

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

target_organs

Respiratory system

Storage Class

10 - Combustible liquids

wgk

WGK 3

flash_point_f

204.8 °F - closed cup

flash_point_c

96 °C - closed cup

ppe

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

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Certificates of Analysis (COA)

Lot/Batch Number
STBL0906
STBK7534
STBK3424
STBK1821
STBB1299V

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Contrasting reactivity in Lewis acid-promoted reactions of thio-and silyl-allenes with 1, 4-benzoquinones.
Tetrahedron Letters, 37(3), 327-330 (1996)
Javier Campanini-Salinas et al.
Molecules (Basel, Switzerland), 23(7) (2018-07-22)
A rapid emergence of resistant bacteria is occurring worldwide, endangering the efficacy of antibiotics and reducing the therapeutic arsenal available for treatment of infectious diseases. In the present study, we developed a new class of compounds with antibacterial activity obtained

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