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About This Item
Linear Formula:
C6H5SO2CH2SCH3
CAS Number:
Molecular Weight:
202.29
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22
assay
99%
mp
85-87 °C (lit.)
SMILES string
CSCS(=O)(=O)c1ccccc1
InChI
1S/C8H10O2S2/c1-11-7-12(9,10)8-5-3-2-4-6-8/h2-6H,7H2,1H3
InChI key
XBGGZYQBIQAYII-UHFFFAOYSA-N
General description
Methylthiomethyl phenyl sulfone is a sulfone derivative.
Application
Methylthiomethyl phenyl sulfone may be employed:
- as nucleophilic and electrophilic building block, in the asymmetric synthesis of 6-N-benzoyl-5′-O-benzyl-2′-deoxyadenosine and its anomer
- in the synthesis of various multidentate methylthio arylethynes (MTA) derivatives
- as starting reagent in the preparation of methylthio arylbutadiynes (Ar-C=C-C=C-SCH3)
signalword
Warning
hcodes
Hazard Classifications
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
target_organs
Respiratory system
Storage Class
11 - Combustible Solids
wgk_germany
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
dust mask type N95 (US), Eyeshields, Gloves
Certificates of Analysis (COA)
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Efficient One-Pot Preparation of Methylthio Arylbutadiynes by Double Elimination Protocol.
Su Q, et al.
Synthetic Communications, 43(19), 2648-2655 (2019)
Rigid, conjugated and shaped arylethynes as mediators for the assembly of gold nanoparticles.
Yan H, et al.
Journal of Materials Chemistry, 21(6), 1890-1901 (2011)
B M Trost et al.
Carbohydrate research, 202, 1-12 (1990-07-15)
An asymmetric synthesis of 6-N-benzoyl-5'-O-benzyl-2'-deoxyadenosine and its a anomer from non-carbohydrate building blocks is achieved in 7 steps. The sequence builds the basic structures using bis(methylthio)methane and methylthiomethyl phenyl sulfone as both nucleophilic and electrophilic building blocks, a feature that
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