540854
4-Isopropylbenzenethiol
95%
Sign In to View Organizational & Contract Pricing.
Select a Size
Change View
About This Item
Linear Formula:
(CH3)2CHC6H4SH
CAS Number:
Molecular Weight:
152.26
NACRES:
NA.22
PubChem Substance ID:
UNSPSC Code:
12352100
MDL number:
assay
95%
refractive index
n20/D 1.552 (lit.)
bp
99-100 °C/14 mmHg (lit.)
density
0.979 g/mL at 25 °C (lit.)
SMILES string
CC(C)c1ccc(S)cc1
InChI
1S/C9H12S/c1-7(2)8-3-5-9(10)6-4-8/h3-7,10H,1-2H3
InChI key
APDUDRFJNCIWAG-UHFFFAOYSA-N
General description
4-Isopropylbenzenethiol is an aromatic thiol. It undergoes oxidation in the presence of activated carbon and xylene to afford the corresponding disulfide. 4-Isopropylbenzenethiol reacts with 2-chloro-3-formylquinolines and NaH in DMSO to afford the corresponding 2-(4-isopropylphenylthio)quinoline-3-carbaldehyde.
Application
4-Isopropylbenzenethiol may be used to synthesize 4-(4-isopropyl-phenylsulfanyl)-benzene-1,2-diol.
signalword
Danger
hcodes
Hazard Classifications
Acute Tox. 4 Oral - Eye Dam. 1 - Skin Corr. 1B
Storage Class
6.1A - Combustible acute toxic Cat. 1 and 2 / very toxic hazardous materials
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Faceshields, Gloves, Goggles, 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.
First construction of 12H-thiochromeno [2, 3-b] quinolines and 5H-benzo [7, 8] thiocino-[2, 3-b] quinolines via intramolecular Friedel-Crafts reaction of Morita-Baylis-Hillman adducts.
Zhong W, et al.
Tetrahedron, 67(19), 3509-3518 (2011)
Oxidative transformation of thiols to disulfides promoted by activated carbon-air system.
Hayashi M, et al.
Tetrahedron Letters, 51(51), 6734-6736 (2010)
Tsuneo Kashiwagi et al.
Chemical communications (Cambridge, England), 48(22), 2806-2808 (2012-02-04)
We have successfully demonstrated that a microflow reactor is extremely useful in controlling reactions involving an unstable o-benzoquinone. The key features of the method are an effective o-benzoquinone generation and its rapid use for the following reaction without decomposition in