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Sulfonate

Index Sulfonate

A sulfonate is a salt or ester of a sulfonic acid. [1]

33 relations: Acid, Adolph Strecker, Base (chemistry), Benzenesulfonic acid, Bissulfosuccinimidyl suberate, Camphorsulfonic acid, Catalysis, Conjugate acid, Ester, Ethanesulfonic acid, Functional group, Haloalkane, Iodide, Ion, Leaving group, Lewis acids and bases, Liebigs Annalen, Mesylate, Methyl group, Methyl trifluoromethanesulfonate, Organic reaction, Oxime, Salt (chemistry), Scandium(III) trifluoromethanesulfonate, Sodium sulfite, Sulfate, Sulfonic acid, Sulfonyl, Sulfoxide, Tosyl, Triflate, Zonisamide, 1,3-Propane sultone.

Acid

An acid is a molecule or ion capable of donating a hydron (proton or hydrogen ion H+), or, alternatively, capable of forming a covalent bond with an electron pair (a Lewis acid).

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Adolph Strecker

Adolph Strecker (October 21, 1822 – November 7, 1871) was a German chemist who is remembered primarily for his work with amino acids.

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Base (chemistry)

In chemistry, bases are substances that, in aqueous solution, release hydroxide (OH−) ions, are slippery to the touch, can taste bitter if an alkali, change the color of indicators (e.g., turn red litmus paper blue), react with acids to form salts, promote certain chemical reactions (base catalysis), accept protons from any proton donor, and/or contain completely or partially displaceable OH− ions.

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Benzenesulfonic acid

Benzenesulfonic acid (conjugate base benzenesulfonate) is an organosulfur compound with the formula C6H5SO3H.

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Bissulfosuccinimidyl suberate

Bissulfosuccinimidyl suberate (BS3) is a crosslinker used in biological research.

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Camphorsulfonic acid

Camphorsulfonic acid, sometimes abbreviated CSA or 10-CSA is an organosulfur compound.

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Catalysis

Catalysis is the increase in the rate of a chemical reaction due to the participation of an additional substance called a catalysthttp://goldbook.iupac.org/C00876.html, which is not consumed in the catalyzed reaction and can continue to act repeatedly.

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Conjugate acid

A conjugate acid, within the Brønsted–Lowry acid–base theory, is a species formed by the reception of a proton (H+) by a base—in other words, it is a base with a hydrogen ion added to it.

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Ester

In chemistry, an ester is a chemical compound derived from an acid (organic or inorganic) in which at least one –OH (hydroxyl) group is replaced by an –O–alkyl (alkoxy) group.

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Ethanesulfonic acid

Ethanesulfonic acid (esylic acid) is a sulfonic acid with the chemical formula CH3CH2SO3H.

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Functional group

In organic chemistry, functional groups are specific substituents or moieties within molecules that are responsible for the characteristic chemical reactions of those molecules.

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Haloalkane

The haloalkanes (also known as halogenoalkanes or alkyl halides) are a group of chemical compounds derived from alkanes containing one or more halogens.

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Iodide

An iodide ion is the ion I−.

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Ion

An ion is an atom or molecule that has a non-zero net electrical charge (its total number of electrons is not equal to its total number of protons).

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Leaving group

In chemistry, a leaving group is a molecular fragment that departs with a pair of electrons in heterolytic bond cleavage.

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Lewis acids and bases

A Lewis acid is a chemical species that contains an empty orbital which is capable of accepting an electron pair from a Lewis base to form a Lewis adduct.

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Liebigs Annalen

Justus Liebigs Annalen der Chemie (often cited as just Liebigs Annalen) was one of the oldest and historically most important journals in the field of organic chemistry worldwide.

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Mesylate

In chemistry, a mesylate is any salt or ester of methanesulfonic acid (CH3SO3H).

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Methyl group

A methyl group is an alkyl derived from methane, containing one carbon atom bonded to three hydrogen atoms — CH3.

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Methyl trifluoromethanesulfonate

Methyl trifluoromethanesulfonate, also commonly called methyl triflate and abbreviated MeOTf, is the organic compound with the formula CF3SO2OCH3.

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Organic reaction

Organic reactions are chemical reactions involving organic compounds.

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Oxime

An oxime is a chemical compound belonging to the imines, with the general formula R1R2C.

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Salt (chemistry)

In chemistry, a salt is an ionic compound that can be formed by the neutralization reaction of an acid and a base.

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Scandium(III) trifluoromethanesulfonate

Scandium trifluoromethanesulfonate, commonly called scandium triflate, is a chemical compound with formula Sc(SO3CF3)3, a salt consisting of scandium cations Sc3+ and triflate SO3CF3− anions.

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Sodium sulfite

Sodium sulfite (sodium sulphite) is a soluble sodium salt of sulfurous acid (sulfite) with the chemical formula Na2SO3.

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Sulfate

The sulfate or sulphate (see spelling differences) ion is a polyatomic anion with the empirical formula.

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Sulfonic acid

A sulfonic acid (or sulphonic acid) refers to a member of the class of organosulfur compounds with the general formula R−S(.

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Sulfonyl

A sulfonyl group can refer either to a functional group found primarily in sulfones or to a substituent obtained from a sulfonic acid by the removal of the hydroxyl group similarly to acyl groups.

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Sulfoxide

A sulfoxide is a chemical compound containing a sulfinyl (SO) functional group attached to two carbon atoms.

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Tosyl

A toluenesulfonyl (shortened tosyl, abbreviated Ts or Tos) group is CH3C6H4SO2.

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Triflate

Triflate, also known by the systematic name trifluoromethanesulfonate, is a functional group with the formula CF3SO3−.

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Zonisamide

Zonisamide is a medication used to treat the symptoms of epilepsy and Parkinson's disease.

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1,3-Propane sultone

1,3-Propane sultone is the organosulfur compound with the formula (CH2)3SO3.

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Strecker sulfite alkylation, Sulfonate anion, Sulfonate ester, Sulfonates, Sulfonato, Sulphonate, Sulphonation, Sultone.

References

[1] https://en.wikipedia.org/wiki/Sulfonate

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