CAS 31562-43-3

tert-Butylsulfinyl chloride

Description:

Tert-Butylsulfinyl chloride, with the CAS number 31562-43-3, is an organosulfur compound characterized by the presence of a tert-butyl group attached to a sulfinyl chloride functional group. This compound typically appears as a colorless to pale yellow liquid and is known for its strong odor. It is soluble in organic solvents such as dichloromethane and ether but is generally insoluble in water due to its hydrophobic tert-butyl moiety. Tert-Butylsulfinyl chloride is reactive, particularly with nucleophiles, and is often used as a reagent in organic synthesis, especially in the preparation of sulfinamides and other sulfur-containing compounds. It can also participate in various substitution reactions, making it valuable in the development of pharmaceuticals and agrochemicals. Due to its reactivity, it should be handled with care, as it can cause irritation to the skin, eyes, and respiratory system. Proper safety measures, including the use of personal protective equipment, are essential when working with this compound.

Formula: C₄H₉ClOS

InChI: InChI=1/C4H9ClOS/c1-4(2,3)7(5)6/h1-3H3

SMILES: CC(C)(C)S(=O)Cl

Synonyms:

• 2-Methylpropane-2-sulfinyl chloride
• 2-Propanesulfinyl Chloride, 2-Methyl-

2-methylpropane-2-sulfinyl chloride

CAS: 31562-43-3

Formula: C₄H₉ClOS

Purity: 97%

Color and Shape: Liquid

Molecular weight: 140.6317

Ref: IN-DA003UM1

Tert-Butylsulfinyl Chloride

CAS: 31562-43-3

Tert-Butylsulfinyl Chloride

Purity: 98%

Molecular weight: 140.63g/mol

Ref: 54-OR1027887

t-Butylsulfinyl chloride

CAS: 31562-43-3

Formula: C₄H₉ClOS

Purity: 97.0%

Color and Shape: Clear

Molecular weight: 140.63

Ref: 10-F094558

tert-Butylsulfinylchloride

CAS: 31562-43-3

Tert-Butylsulfinylchloride is a hydroxamic acid that has been shown to be an effective inhibitor of indole alkaloids, such as tryptamine and serotonin. This compound is enantiopure and chiral, which allows for the synthesis of a number of diastereomers. Tert-Butylsulfinylchloride can react with hydrogen peroxide to form reactive intermediates that are thought to have a mechanistic role in the inhibition of indole alkaloid biosynthesis. It also reacts with chloride under thermal conditions to produce an asymmetric synthesis. Tert-Butylsulfinylchloride can be used at temperatures up to 125 degrees Celsius without losing its anti-indole alkaloid properties, making it a good candidate for use in organic syntheses.

Formula: C₄H₉ClOS

Purity: Min. 95%

Color and Shape: Clear Liquid

Molecular weight: 140.63 g/mol

Ref: 3D-FB147204