Skip to Content
Merck
CN

65357

4-Methoxythiophenol

purum, ≥98.0% (GC)

Synonym(s):

4-Mercaptoanisole, 4-Methoxybenzenethiol

Sign In to View Organizational & Contract Pricing.

Select a Size

About This Item

Linear Formula:
CH3OC6H4SH
CAS Number:
696-63-9
Molecular Weight:
140.20
EC Number:
211-799-2
UNSPSC Code:
12352100
PubChem Substance ID:
329760050
Beilstein/REAXYS Number:
1446910
MDL number:
MFCD00004849

Key Documents

View All Documentation
Technical Service
Need help? Our team of experienced scientists is here for you.
Let Us Assist
Technical Service
Need help? Our team of experienced scientists is here for you.
Let Us Assist

grade

purum

assay

≥98.0% (GC)

refractive index

n20/D 1.5831 (lit.), n20/D 1.584

bp

100-103 °C/13 mmHg (lit.)

density

1.14 g/mL at 25 °C (lit.)

SMILES string

COc1ccc(S)cc1

InChI

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

InChI key

NIFAOMSJMGEFTQ-UHFFFAOYSA-N

pictograms

Exclamation mark
GHS07

signalword

Warning

Hazard Classifications

Acute Tox. 4 Dermal - Acute Tox. 4 Inhalation - Acute Tox. 4 Oral - 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

Regulatory Information

新产品

This item has

Choose from one of the most recent versions:

Certificates of Analysis (COA)

Lot/Batch Number

It looks like we've run into a problem, but you can still download Certificates of Analysis from our Documents section.

If you need assistance, please contact Customer Support

Already Own This Product?

Find documentation for the products that you have recently purchased in the Document Library.

Visit the Document Library

Hadeel T Al-Sinjilawi et al.
Archiv der Pharmazie, 347(11), 861-872 (2014-09-16)
A series of substituted 4-oxopyrido[2,3-a]phenothiazine-3-carboxylic acids (6a-d) were prepared via cyclization of the corresponding ethyl 7-(arylthioxy)-8-nitro(or azido)-4-oxoquinoline-3-carboxylates (3a-d/4a-d), followed by hydrolysis of the resultant esters (5a-d). Among these tetracyclics, compound 6a with unsubstituted terminal benzo-ring D was the most active

Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.

Contact Technical Service