CAS 6553-96-4

2,4,6-Tris(1-methylethyl)benzenesulfonyl chloride

Description:

2,4,6-Tris(1-methylethyl)benzenesulfonyl chloride, with the CAS number 6553-96-4, is an organic compound characterized by its sulfonyl chloride functional group attached to a benzene ring that is further substituted with three isopropyl groups. This structure imparts significant steric hindrance, influencing its reactivity and solubility. The sulfonyl chloride group is known for its high reactivity, particularly in nucleophilic substitution reactions, making this compound useful in organic synthesis, especially for the introduction of sulfonyl groups into various substrates. It is typically a colorless to pale yellow liquid or solid, depending on its purity and form. The compound is sensitive to moisture, as it can hydrolyze to form the corresponding sulfonic acid. Safety precautions are necessary when handling this substance, as it can be corrosive and irritating to skin and mucous membranes. Proper storage in a cool, dry place, away from moisture and incompatible substances, is essential to maintain its stability and reactivity.

Formula: C₁₅H₂₃ClO₂S

InChI: InChI=1S/C15H23ClO2S/c1-9(2)12-7-13(10(3)4)15(19(16,17)18)14(8-12)11(5)6/h7-11H,1-6H3

InChI key: InChIKey=JAPYIBBSTJFDAK-UHFFFAOYSA-N

SMILES: S(Cl)(=O)(=O)C1=C(C(C)C)C=C(C(C)C)C=C1C(C)C

Synonyms:

• 2,4,6-Tri(Propan-2-Yl)Benzenesulfonyl Chloride
• 2,4,6-Triisopropybenzenesulfonyl*Chloride
• 2,4,6-Triisopropylbenzene-1-sulfonyl chloride
• 2,4,6-Triisopropylbenzenesulfonoyl chloride
• 2,4,6-Triisopropylphenylsulfonyl chloride
• 2,4,6-Tris(1-methylethyl)benzenesulfonyl chloride
• 2,4,6-Tris(isopropyl)benzenesulfonyl chloride
• Benzenesulfonyl chloride, 2,4,6-triisopropyl-
• Benzenesulfonyl chloride, 2,4,6-tris(1-methylethyl)-
• NSC 102803
• Tpscl
• Tripsyl chloride

2,4,6-Triisopropylbenzenesulfonyl Chloride

CAS: 6553-96-4

Formula: C₁₅H₂₃ClO₂S

Purity: >97.0%(T)

Color and Shape: White powder to lump

Molecular weight: 302.86

Ref: 3B-T0459

2,4,6-Triisopropylbenzenesulfonyl chloride, 98%

CAS: 6553-96-4

2,4,6-Triisopropylbenzenesulfonyl chloride is used for the synthesis of glycerophospholipids as a condensing agent and in the analysis of phosphonolipids in egg yolk by HPLC/MS technique. It acts as a coupling reagent for the synthesis of oligonucleotides and as sulfonates of pyrimidine nucleosides.

Formula: C₁₅H₂₃ClO₂S

Purity: 98%

Color and Shape: Crystals or powder or crystalline powder, White to pale pink to pale cream

Molecular weight: 302.86

Ref: 02-A11458

2,4,6-Triisopropylbenzene-1-sulfonyl chloride

CAS: 6553-96-4

Formula: C₁₅H₂₃ClO₂S

Purity: 98%

Color and Shape: Solid

Molecular weight: 302.8599

Ref: IN-DA0032YM

2,4,6-Triisopropylbenzenesulfonyl chloride

CAS: 6553-96-4

Formula: C₁₅H₂₃ClO₂S

Molecular weight: 302.87

Ref: 7W-GK2646

2,4,6-Tris(isopropyl)benzenesulphonyl chloride

CAS: 6553-96-4

2,4,6-Tris(isopropyl)benzenesulphonyl chloride

Formula: C₁₅H₂₃ClO₂S

Purity: 98%

Color and Shape: white to off white solid

Molecular weight: 302.86g/mol

Ref: 54-OR5360

2,4,6-Triisopropylbenzenesulfonyl chloride

CAS: 6553-96-4

2,4,6-Triisopropylbenzenesulfonyl chloride is a molecule that belongs to the class of ethylene diamine. It has been shown to inhibit the replication of herpes simplex virus in cell culture. This compound has an intramolecular hydrogen and steric interactions with a hydroxyl group. The analog of this molecule is 2,4,6-triisopropylbenzenesulfonic acid.
2,4,6-Triisopropylbenzenesulfonyl chloride can be used as a sulfonation agent and is known for its ability to react with nitrogen nucleophiles such as amines or ammonia.

Formula: C₁₅H₂₃SO₂Cl

Purity: Min. 95%

Molecular weight: 302.86 g/mol

Ref: 3D-FT47022

2,4,6-Triisopropylbenzenesulfonyl chloride

CAS: 6553-96-4

Formula: C₁₅H₂₃ClO₂S

Purity: 97%

Color and Shape: Solid, Clear

Molecular weight: 302.86

Ref: 10-F003615

2,4,6-Triisopropylbenzenesulfonyl Chloride

Controlled Product

CAS: 6553-96-4

Applications 2,4,6-Triisopropylbenzenesulfonyl Chloride, is a building block used for the synthesis of various pharmaceutical compounds, such as derivatives of Valproic Acid (V094750). It can also be used for the synthesis of glycerophospholipids as a condensing agent.
Not a dangerous good if item is equal to or less than 1g/ml and there is less than 100g/ml in the package
References Aneja, R., et al.: Biochimica et Biophysica Acta, 218, 102 (1970); Loscher, W., Prog. Neurobiol., 58, 31 (1999);

Formula: C₁₅H₂₃ClO₂S

Color and Shape: Neat

Molecular weight: 302.86

Ref: TR-T795575