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Sodium methanesulfinate

Basic information Description Safety Supplier Related

Sodium methanesulfinate Basic information

Product Name:
Sodium methanesulfinate
Synonyms:
  • Sodium methanesulfinate,Methanesulfinic acid sodium salt
  • Sodium methanesulphinate, tech
  • Methanesulfinic acid,sodiuM salt (1:1)
  • Sodium methanesulphinate Methanesulfinic acid sodium salt
  • Sodium methanesulfinate technical grade, 85%
  • Sodium methylsulfinate
  • METHANESULPHINIC ACID SODIUM SALT
  • METHANESULFINIC ACID
CAS:
20277-69-4
MF:
CH5NaO2S
MW:
104.1
EINECS:
243-669-6
Product Categories:
  • Aliphatics
Mol File:
20277-69-4.mol
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Sodium methanesulfinate Chemical Properties

Melting point:
222-226 °C (dec.) (lit.)
storage temp. 
Inert atmosphere,Room Temperature
solubility 
Methanol, Water (Slightly)
form 
Powder
color 
White to light beige
Water Solubility 
soluble
Sensitive 
Air Sensitive & Hygroscopic
BRN 
3565430
Stability:
Hygroscopic
InChI
InChI=1S/CH4O2S.Na.H/c1-4(2)3;;/h1H3,(H,2,3);;
InChIKey
LYPGDCWPTHTUDO-UHFFFAOYSA-M
SMILES
S(O)(=O)C.[NaH]
CAS DataBase Reference
20277-69-4(CAS DataBase Reference)
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Safety Information

Hazard Codes 
Xn
Risk Statements 
22-20/21/22
Safety Statements 
36/37-24/25
RIDADR 
2811
WGK Germany 
3
PackingGroup 
III
HS Code 
29309090

MSDS

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Sodium methanesulfinate Usage And Synthesis

Description

Sodium methanesulfinate is an aliphatic sodium sulfinate. Conjugate addition of sodium methanesulfinate to vinyl heterocycles has been described. Cross-coupling reaction between aryl boronic acid and sodium methanesulfinate has been studied. It can be used in the preparation of alkyl methyl sulfone and methyl bis(4-tolyl)sulfoniumtrifluoromethanesulfonate. It is also employed in the synthesis of two sulfonyl type reversible addition-fragmentation transfer (RAFT) agents such as benzyl methylsulfonyldithioformate and benzyl phenylsulfonyldithioformate. Moreover, it can be used for synthesizing cyclooxygenase-2 inhibitors.

Chemical Properties

White to light beige powder

Uses

Sodium methylsulfinate can be used to synthesize cyclooxygenase-2 inhibitors.

General Description

Sodium methanesulfinate is an aliphatic sodium sulfinate. Conjugate addition of sodium methanesulfinate to vinyl heterocycles has been described. Cross-coupling reaction between aryl boronic acid and sodium methanesulfinate has been studied. Its stock solution was prepared from methanesulfonic acid by adding one equivalent of sodium hydroxide and diluting it to 4M.

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