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873-55-2,MFCD00149638
Catalog No.:AA004KPH

873-55-2 | Sodium benzenesulfinate

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10g
95%
in stock  
$6.00   $4.00
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25g
95%
in stock  
$13.00   $9.00
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100g
95%
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$23.00   $16.00
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500g
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  • Technical Information
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  • Technical Information
  • Properties
  • Literature
Technical Information
Catalog Number:
AA004KPH
Chemical Name:
Sodium benzenesulfinate
CAS Number:
873-55-2
Molecular Formula:
C6H5NaO2S
Molecular Weight:
164.1575
MDL Number:
MFCD00149638
SMILES:
[O-]S(=O)c1ccccc1.[Na+]
Properties
Properties
 
BP:
339.4°C at 760 mmHg  
Form:
Solid  
MP:
>300 °C(lit.)  
Stability:
Hygroscopic  
Storage:
Inert atmosphere;Room Temperature;  

Computed Properties
 
Complexity:
112  
Covalently-Bonded Unit Count:
2  
Heavy Atom Count:
10  
Hydrogen Bond Acceptor Count:
3  
Rotatable Bond Count:
1  

Literature

Title: Palladium-catalyzed conjugate addition to electron-deficient alkynes with benzenesulfinic acid derived from 1,2-bis(phenylsulfonyl)ethane: selective synthesis of (E)-vinyl sulfones.

Journal: The Journal of organic chemistry 20110204

Title: Stereocontrolled synthesis of the D- and L-glycero-beta-D-manno-heptopyranosides and their 6-deoxy analogues. Synthesis of methyl alpha-l-rhamno-pyranosyl-(1-->3)-D-glycero-beta-D-manno-heptopyranosyl- (1-->3)-6-deoxy-glycero-beta-D-manno-heptopyranosyl-(1-->4)-alpha-L- rhamno-pyranoside, a tetrasaccharide subunit of the lipopolysaccharide from Plesimonas shigelloides.

Journal: Journal of the American Chemical Society 20060621

Title: S,O-acetals as novel 'chiral aldehyde' equivalents.

Journal: Chemistry (Weinheim an der Bergstrasse, Germany) 20060301

Title: A facile solid-phase synthesis of 1,2,4,5-tetrasubstituted imidazoles using sodium benzenesulfinate as a traceless linker.

Journal: Journal of combinatorial chemistry 20050101

Title: Solid-phase synthesis of 3,4-dihydro-1H-pyrimidine-2-ones using sodium benzenesulfinate as a traceless linker.

Journal: Journal of combinatorial chemistry 20050101

Title: 1-Benzenesulfinyl piperidine/trifluoromethanesulfonic anhydride: a potent combination of shelf-stable reagents for the low-temperature conversion of thioglycosides to glycosyl triflates and for the formation of diverse glycosidic linkages.

Journal: Journal of the American Chemical Society 20010919

Title: Interfacial study of benzenesulfinate chemisorbed on silver.

Journal: Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy 20010101

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