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873-55-2 | Sodium benzenesulfinate
CAS No: 873-55-2 Catalog No: AG004KS9 MDL No:MFCD00013135
Product Description
Catalog Number:
AG004KS9
Chemical Name:
Sodium benzenesulfinate
CAS Number:
873-55-2
Molecular Formula:
C6H5NaO2S
Molecular Weight:
164.1575
MDL Number:
MFCD00013135
IUPAC Name:
sodium;benzenesulfinate
InChI:
InChI=1S/C6H6O2S.Na/c7-9(8)6-4-2-1-3-5-6;/h1-5H,(H,7,8);/q;+1/p-1
InChI Key:
CHLCPTJLUJHDBO-UHFFFAOYSA-M
SMILES:
[O-]S(=O)c1ccccc1.[Na+]
EC Number:
212-842-8
Properties
Complexity:
112
Compound Is Canonicalized:
Yes
Covalently-Bonded Unit Count:
2
Defined Atom Stereocenter Count:
0
Defined Bond Stereocenter Count:
0
Exact Mass:
163.991g/mol
Formal Charge:
0
Heavy Atom Count:
10
Hydrogen Bond Acceptor Count:
3
Hydrogen Bond Donor Count:
0
Isotope Atom Count:
0
Molecular Weight:
164.154g/mol
Monoisotopic Mass:
163.991g/mol
Rotatable Bond Count:
1
Topological Polar Surface Area:
59.3A^2
Undefined Atom Stereocenter Count:
0
Undefined Bond Stereocenter Count:
0
Literature
| Title | Journal |
|---|---|
| Palladium-catalyzed conjugate addition to electron-deficient alkynes with benzenesulfinic acid derived from 1,2-bis(phenylsulfonyl)ethane: selective synthesis of (E)-vinyl sulfones. | The Journal of organic chemistry 20110204 |
| 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 of the American Chemical Society 20060621 |
| S,O-acetals as novel 'chiral aldehyde' equivalents. | Chemistry (Weinheim an der Bergstrasse, Germany) 20060301 |
| A facile solid-phase synthesis of 1,2,4,5-tetrasubstituted imidazoles using sodium benzenesulfinate as a traceless linker. | Journal of combinatorial chemistry 20050101 |
| Solid-phase synthesis of 3,4-dihydro-1H-pyrimidine-2-ones using sodium benzenesulfinate as a traceless linker. | Journal of combinatorial chemistry 20050101 |
| 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 of the American Chemical Society 20010919 |
| Interfacial study of benzenesulfinate chemisorbed on silver. | Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy 20010101 |
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