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155705

Sigma-Aldrich

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
Beilstein:
2041496
EC Number:
239-617-7
MDL number:
MFCD00004841
UNSPSC Code:
12352100
PubChem Substance ID:
24849559
NACRES:
NA.22

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

SMILES string

COc1cccc(S)c1

InChI

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

InChI key

QMVAZEHZOPDGHA-UHFFFAOYSA-N

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Application

3-Methoxythiophenol was used in the preparation of allenes.

Pictograms

Exclamation mark
GHS07

Signal Word

Warning

Hazard Statements

H315 - H319 - H335

Hazard Classifications

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

Target Organs

Respiratory system

Storage Class Code

10 - Combustible liquids

WGK

WGK 3

Flash Point(F)

204.8 °F - closed cup

Flash Point(C)

96 °C - closed cup

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Regulatory Listings

Regulatory Listings are mainly provided for chemical products. Only limited information can be provided here for non-chemical products. No entry means none of the components are listed. It is the user’s obligation to ensure the safe and legal use of the product.

FSL

Flammable liquids
Type 3 petroleums
Hazardous rank III
Water insoluble liquid

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

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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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