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Brc1cnc(nc1)C
Pyrimidine, 5-bromo-2-methyl-
CCCP1(=O)OP(=O)(CCC)OP(=O)(O1)CCC
1,3,5,2,4,6-Trioxatriphosphorinane, 2,4,6-tripropyl-, 2,4,6-trioxide
CC1(C)OB(OC1(C)C)B1OC(C(O1)(C)C)(C)C
2,2'-Bi-1,3,2-dioxaborolane, 4,4,4',4',5,5,5',5'-octamethyl-
O=C(C=Cc1ccccc1)C=Cc1ccccc1.O=C(C=Cc1ccccc1)C=Cc1ccccc1.O=C(C=Cc1ccccc1)C=Cc1ccccc1.[Pd].[Pd]
Tris(dibenzylideneacetone)dipalladium
C1CCC(CC1)P(C1CCCCC1)C1CCCCC1.Cc1cc(C)c(c(c1)C)N1CCN(C1=[Ru](=Cc1ccccc1)(Cl)Cl)c1c(C)cc(cc1C)C
Ruthenium,[1,3-bis(2,4,6-trimethylphenyl)-2-imidazolidinylidene]dichloro(phenylmethylene)(tricyclohexylphosphine)-, (SP-5-41)-

sodium;ethanesulfinate

[O-]S(=O)CC.[Na+] Request for Quotation
Chemical Name: sodium;ethanesulfinate
CAS Number: 20035-08-9
Product Number: AG002CPH(AGN-PC-03XQ0B)
Synonyms:
MDL No:
Molecular Formula: C2H5NaO2S
Molecular Weight: 116.1147

Identification/Properties

Properties
MP:
292 °C
BP:
244°C at 760 mmHg
Storage:
Inert atmosphere;Room Temperature;
Form:
Solid
Computed Properties
Molecular Weight:
116.11g/mol
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
1
Exact Mass:
115.991g/mol
Monoisotopic Mass:
115.991g/mol
Topological Polar Surface Area:
59.3A^2
Heavy Atom Count:
6
Formal Charge:
0
Complexity:
46.8
Isotope Atom Count:
0
Defined Atom Stereocenter Count:
0
Undefined Atom Stereocenter Count:
0
Defined Bond Stereocenter Count:
0
Undefined Bond Stereocenter Count:
0
Covalently-Bonded Unit Count:
2
Compound Is Canonicalized:
Yes

Safety Information

GHS Pictogram:
Signal Word:
Warning
UN#:
N/A
Hazard Statements:
H302-H315-H319-H335
Precautionary Statements:
P261-P305+P351+P338
Class:
N/A
Packing Group:
N/A

NMR Spectrum

Other Analytical Data

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Chemical Structure


Sodium Ethanesulfinate is a versatile chemical reagent commonly used in chemical synthesis processes. Its primary application lies in its ability to act as a mild reducing agent, facilitating various reactions in organic chemistry. When utilized in synthesis, this compound can effectively reduce organic functional groups such as ketones, aldehydes, and olefins, leading to the formation of alcohol or alkane products. Furthermore, Sodium Ethanesulfinate can serve as a key component in the selective reduction of certain functional groups in complex molecules, allowing chemists to target specific sites for modification while leaving other parts of the molecule untouched. Its mild nature makes it particularly useful in scenarios where harsher reducing agents might cause unwanted side reactions or damage sensitive functional groups. Overall, Sodium Ethanesulfinate plays a crucial role in the realm of chemical synthesis by providing a reliable and selective method for reducing organic compounds in a controlled manner. Its versatility and effectiveness make it a valuable tool for chemists working on the synthesis of organic molecules for various applications across industries.