Sign In to View Organizational & Contract Pricing.
Select a Size
About This Item
Linear Formula:
CH3SC6H4NH2
CAS Number:
Molecular Weight:
139.22
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
221-055-9
Beilstein/REAXYS Number:
386211
MDL number:
Assay:
97%
InChI key
WBRPQQSADOCKCH-UHFFFAOYSA-N
InChI
1S/C7H9NS/c1-9-7-5-3-2-4-6(7)8/h2-5H,8H2,1H3
SMILES string
CSc1ccccc1N
assay
97%
refractive index
n20/D 1.624 (lit.)
bp
234 °C (lit.)
density
1.111 g/mL at 25 °C (lit.)
Quality Level
Related Categories
signalword
Danger
hcodes
pcodes
Hazard Classifications
Acute Tox. 3 Oral
Storage Class
6.1C - Combustible acute toxic Cat.3 / toxic compounds or compounds which causing chronic effects
wgk
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
Regulatory Information
新产品
This item has
Choose from one of the most recent versions:
Already Own This Product?
Find documentation for the products that you have recently purchased in the Document Library.
Thioether sulfur-bound [Cu2] complexes showing catechol oxidase activity and DNA cleaving behaviour.
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
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