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Merck

368539

Sigma-Aldrich

甲硫甲基苯基砜

99%

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About This Item

线性分子式:
C6H5SO2CH2SCH3
CAS号:
分子量:
202.29
MDL號碼:
分類程式碼代碼:
12352100
PubChem物質ID:
NACRES:
NA.22

化驗

99%

mp

85-87 °C (lit.)

SMILES 字串

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 密鑰

XBGGZYQBIQAYII-UHFFFAOYSA-N

一般說明

Methylthiomethyl phenyl sulfone is a sulfone derivative.

應用

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)

象形圖

Exclamation mark

訊號詞

Warning

危險聲明

危險分類

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

標靶器官

Respiratory system

儲存類別代碼

11 - Combustible Solids

水污染物質分類(WGK)

WGK 3

閃點(°F)

Not applicable

閃點(°C)

Not applicable

個人防護裝備

dust mask type N95 (US), Eyeshields, Gloves


历史批次信息供参考:

分析证书(COA)

Lot/Batch Number

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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)
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
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)

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