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Merck
CN

339997

(S)-(-)-甲基对甲苯亚砜

99%

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关于此项目

线性分子式:
CH3C6H4S(O)CH3
化学文摘社编号:
分子量:
154.23
UNSPSC Code:
12191600
NACRES:
NA.22
PubChem Substance ID:
MDL number:
Beilstein/REAXYS Number:
2324696
Assay:
99%
Form:
solid
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Quality Segment

assay

99%

form

solid

optical activity

[α]20/D −145°, c = 2 in acetone

optical purity

ee: 99% (HPLC)

mp

75-77 °C (lit.)

SMILES string

Cc1ccc(cc1)S(C)=O

InChI

1S/C8H10OS/c1-7-3-5-8(6-4-7)10(2)9/h3-6H,1-2H3/t10-/m0/s1

InChI key

FEVALTJSQBFLEU-JTQLQIEISA-N

Application

(S)-(-)-Methyl p-tolyl sulfoxide can be used as a nucleophilic reagent to synthesize:
  • Optically active β-disulfoxides by reacting with arenesulfinic esters via formation of α-sulfinylcarbanion.
  • α-substituted N-hydroxylamines by treating with nitrones via preparation of (S)-(-)-methyl p-tolyl sulfoxide anion.
  • 2-O-benzyl-3,4-O-isopropylidene-L-erythrose by one-carbon homologation of 2,3-O-isopropylidene-L-glyceraldehyde.



存储类别

11 - Combustible Solids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Gloves, type N95 (US)



历史批次信息供参考:

分析证书(COA)

Lot/Batch Number

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