CAS 14752-66-0

Benzenesulfinic acid, 4-chloro-, sodium salt (1:1)

Description:

Benzenesulfinic acid, 4-chloro-, sodium salt (1:1) is an organosulfur compound characterized by the presence of a sulfinic acid functional group attached to a benzene ring that also features a chlorine substituent at the para position. This compound is typically encountered as a white to off-white crystalline solid, which is soluble in water due to the presence of the sodium salt. The sulfinic acid group imparts acidic properties, allowing it to participate in various chemical reactions, including nucleophilic substitutions and redox reactions. Its chlorine substituent can influence the reactivity and stability of the compound, making it useful in synthetic organic chemistry. Additionally, benzenesulfinic acids are often employed as intermediates in the synthesis of dyes, pharmaceuticals, and agrochemicals. Safety data indicates that, like many chemical substances, it should be handled with care, as it may pose health risks if ingested or inhaled. Proper laboratory practices and safety protocols should be followed when working with this compound.

Formula: C₆H₄ClNaO₂S

InChI: InChI=1/C6H5ClO2S.Na/c7-5-1-3-6(4-2-5)10(8)9;/h1-4H,(H,8,9);/q;+1/p-1

InChI key: InChIKey=GJAKRMFICWCSQW-UHFFFAOYSA-N

SMILES: S(=O)(O)C1=CC=C(Cl)C=C1.[Na]

Synonyms:

• 4-Chlorobenzenesulfinate
• 4-Chlorobenzenesulfinic acid sodium salt
• 4-Chlorobenzenesulfinic acid sodium salt hydrate
• 4-Chlorobenzenesulfinic acid sodium salt4
• Benzenesulfinic acid, 4-chloro-, sodium salt
• Benzenesulfinic acid, 4-chloro-, sodium salt (1:1)
• Benzenesulfinic acid, p-chloro-, sodium salt
• NSC 67146
• Sodium 4-Chlorobenzenesulfinate
• Sodium 4-chlorophenylsulfinate
• Sodium p-chlorobenzenesulfinate
• Sodium p-chlorophenylsulfinate
• Sodium 4-chlorobenzenesulphinate
• 4-Chlorobenzenesulfinic acid hydrate sodium salt
• Sodium 4-chlorobenzenesulfinate hydrate
• SODIUM 4-CHLOROBENZENE SULFINIC ACID
• sodium p-chlorobenzenesulphinate
• 4-CHLOROBENZENESULPHINIC ACID SODIUM SALT
• P-CHLOROBENZENESULFINIC ACID SODIUM SALT
• 4-Chlorobenzenesulfinic acid sodium salt, 97+%

Sodium 4-Chlorobenzenesulfinate

CAS: 14752-66-0

Formula: C₆H₄ClNaO₂S

Purity: >98.0%(T)

Color and Shape: White to Light yellow powder to crystal

Molecular weight: 198.60

Ref: 3B-C1559

4-Chlorobenzenesulfinic acid sodium salt hydrate, 97%

CAS: 14752-66-0

This Thermo Scientific Chemicals brand product was originally part of the Alfa Aesar product portfolio. Some documentation and label information may refer to the legacy brand. The original Alfa Aesar product / item code or SKU reference has not changed as a part of the brand transition to Thermo Sci

Formula: C₆H₄ClNaO₂S

Purity: 97%

Color and Shape: Crystals or powder or crystalline powder, White

Molecular weight: 198.60

Ref: 02-A12583

Benzenesulfinic acid, 4-chloro-, sodium salt (1:1)

CAS: 14752-66-0

Formula: C₆H₄ClNaO₂S

Purity: 98%

Color and Shape: Solid

Molecular weight: 198.6025

Ref: IN-DA001EYT

Sodium 4-chlorobenzenesulfinate

CAS: 14752-66-0

Sodium 4-chlorobenzenesulfinate

Purity: 98%

Molecular weight: 198.60g/mol

Ref: 54-OR80184

4-Chlorobenzenesulfinic acid sodium salt

CAS: 14752-66-0

Formula: C₆H₄ClNaO₂S

Purity: 95%

Color and Shape: Solid

Molecular weight: 198.6

Ref: 10-F005929

4-Chloro-benzene-sulfinic acid sodium salt

CAS: 14752-66-0

The 4-chloro-benzenesulfinic acid sodium salt is a type of sulfinic acid. It can be used to control experiments involving methides, halides, and human macrophages. Sodium salts of this compound have been shown to inhibit the growth of Candida glabrata and Galleria mellonella in vitro. The 4-chloro-benzenesulfinic acid sodium salt reacts with chloride ion to form a nucleophilic trifluoroacetate anion, which reacts with thiosulfonates to produce type strain. Trifluoroacetic acid is used as a solvent in the reaction.

Formula: C₆H₄ClNaO₂S

Purity: Min. 95%

Molecular weight: 198.6 g/mol

Ref: 3D-FC02150