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(R)-(+)-Methyl p-tolyl sulfoxide

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(R)-(+)-Methyl p-tolyl sulfoxide Basic information

Product Name:
(R)-(+)-Methyl p-tolyl sulfoxide
Synonyms:
  • (R)-(+)-METHYL P-TOLYL SULFOXIDE
  • (R)-methyl4-methylphenylsulfoxide
  • 1-Methanesulfinyl-4-methyl-benzene
  • (R)-1-Methyl-4-(Methylsulfinyl)benzene
  • (R)-(+)-Methyl p-tolyl sulfoxide 99%
  • Benzene, 1-methyl-4-[(R)-methylsulfinyl]-
  • 1-methyl-4-[(R)-methylsulfinyl]benzene
CAS:
1519-39-7
MF:
C8H10OS
MW:
154.23
Product Categories:
  • Chiral Compound
  • Chiral Building Blocks
  • Organic Building Blocks
  • Sulfoxides
Mol File:
1519-39-7.mol
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(R)-(+)-Methyl p-tolyl sulfoxide Chemical Properties

Melting point:
73-75 °C(lit.)
Boiling point:
247.62°C (rough estimate)
alpha 
145 º (c=2, acetone)
Density 
1.1125 (rough estimate)
refractive index 
1.5780 (estimate)
form 
Solid
optical activity
[α]20/D +145°, c = 2 in acetone
BRN 
2040677
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Safety Information

Safety Statements 
22-24/25
WGK Germany 
3
3-10
HS Code 
2930909899

MSDS

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(R)-(+)-Methyl p-tolyl sulfoxide Usage And Synthesis

Uses

Used in asymmetric synthesis; adds diastereoselectively to carbony compounds, esters, imines, nitrones, and nitrile oxides.

General Description

(R)-(+)-Methyl p-tolyl sulfoxide may be used to prepare (R)-(+)-methyl 3,5-dimethoxy-6-[8-oxo-9-(p-tolylsulfinyl) nonyl] benzoate, an intermediate for (R)-lasiodiplodin synthesis. Its anions undergo addition reaction with nitrones to form optically active a-substituted N-hydroxylamines. (R)-(+)-Methyl p-tolyl sulfoxide also reacts with O-mesitylsulfonylhydroxylamine (MSH) to form (-)-(R)-S-methyl-S-p-tolylsulfoximine.

Synthesis

(R)-(+)-Methyl p-tolyl sulfoxide is prepared by the nucleophilic displacement of (-)- (1R,2S,5R)-Menthyl (S)-p-Toluenesulfinate with methyl Grignard with complete inversion of configuration at sulfur (eq 1).

Synthesis

Highly sensitive to air and moisture. Its generation and handling must be carried out under an inert atmosphere of nitrogen or argon. Normally, preparation is carried out immediately prior to use.

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