2514-70-7

Basic information

• Product Name: benzenesulfonic acid [3-phenylsulfonyloxy-2,2-bis(phenylsulfonyloxymethyl)propyl] ester
• Synonyms: [3-phenylsulfonyloxy-2,2-bis(phenylsulfonyloxymethyl)propyl] benzenesulfonate;benzenesulfonic acid [3-phenylsulfonyloxy-2,2-bis(phenylsulfonyloxymethyl)propyl] ester;USQQFBRJEIDVBV-UHFFFAOYSA-N
• CAS NO: 2514-70-7
• Molecular Formula: C₂₉H₂₈O₈S₄
• Molecular Weight: 696.78542
• Mol File: 2514-70-7.mol

Chemical Properties

• Boiling Point: 855°Cat760mmHg
• Flash Point: 470.9°C
• Appearance: /
• Density: 1.447g/cm³
• Vapor Pressure: 1.94E-28mmHg at 25°C
• Refractive Index: 1.607
• CAS DataBase Reference: benzenesulfonic acid [3-phenylsulfonyloxy-2,2-bis(phenylsulfonyloxymethyl)propyl] ester(CAS DataBase Reference)
• NIST Chemistry Reference: benzenesulfonic acid [3-phenylsulfonyloxy-2,2-bis(phenylsulfonyloxymethyl)propyl] ester(2514-70-7)
• EPA Substance Registry System: benzenesulfonic acid [3-phenylsulfonyloxy-2,2-bis(phenylsulfonyloxymethyl)propyl] ester(2514-70-7)

Safety Data

• Hazardous Substances Data: 2514-70-7(Hazardous Substances Data)

Usage

Uses

Used in Polymer and Plastic Production:
Benzenesulfonic acid [3-phenylsulfonyloxy-2,2-bis(phenylsulfonyloxymethyl)propyl] ester is used as a coupling agent in the manufacturing of polymers and plastics. Its strong bonding capabilities enhance the durability and flexibility of these materials.
Used in Adhesive Production:
This chemical is also used in the production of adhesives, where it acts as a coupling agent to improve the adhesive's bonding strength and stability.
Used in Dye Manufacturing:
Benzenesulfonic acid [3-phenylsulfonyloxy-2,2-bis(phenylsulfonyloxymethyl)propyl] ester is utilized as a coupling agent in the manufacturing of dyes, contributing to the colorfastness and stability of the dyes.
Used in Pharmaceutical Synthesis:
In the pharmaceutical industry, this chemical serves as an important intermediate in the synthesis of various drugs, playing a crucial role in the development of new medications.
Used as a Heat Stabilizer in PVC Production:
Due to its high thermal stability, benzenesulfonic acid [3-phenylsulfonyloxy-2,2-bis(phenylsulfonyloxymethyl)propyl] ester is used as a heat stabilizer in the production of PVC, preventing the degradation of PVC at high temperatures.
Used as a Plasticizer in Polymer Production:
This chemical is also used as a plasticizer in the production of PVC and other polymers, improving their flexibility and durability.
While benzenesulfonic acid [3-phenylsulfonyloxy-2,2-bis(phenylsulfonyloxymethyl)propyl] ester is considered to be relatively stable and has low toxicity, it is essential to follow proper handling and storage procedures to minimize any potential health or environmental risks.

InChI:InChI=1/C29H28O12S4/c30-42(31,25-13-5-1-6-14-25)38-21-29(22-39-43(32,33)26-15-7-2-8-16-26,23-40-44(34,35)27-17-9-3-10-18-27)24-41-45(36,37)28-19-11-4-12-20-28/h1-20H,21-24H2

Upstream product

• 115-77-5 Pentaerythritol 
• 98-59-9 p-toluenesulfonyl chloride 
• 98-09-9 benzenesulfonyl chloride 
• 16873-35-1 1,3-bis-phenylsulfanyl-2,2-bis-phenylsulfanylmethyl-propane 

Downstream Products

• 3229-00-3 pentaerythritol tetrabromide 
• 3221-64-5 1,1,1,1-tetrakis[(2-salicylaldimino)methyl]methane 
• 14302-75-1 2,2-bis(aminomethyl)propane-1,3-diamine tetrahydrochloride 
• 1443793-84-7 C₅₃H₄₈N₄O₈S₄ 
• 381670-43-5 4-{2,2-bis[(4-formylphenoxy)methyl]-3-(4-formylphenoxy)propoxy}benzaldehyde 
• 3057-91-8 spiro[3.3]heptane-2,6-dicarboxylic acid 
• 342886-91-3 6,6-bis-(5-amino-2-azapentyl)-1,11-diamino-4,8-diazaundecane 

Relevant articles and documents

A bright entry to improve the performance of DSSCs with the influence of novel optoelectronic acridinedione based macromolecules in I-/I 3- electrolytes

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Synthesis, crystal structure and luminescence properties of homodinuclear lanthanide complexes with a new tetrapodal thenylsalicylamide ligand

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Cyclobutane-derived diamines: Synthesis and molecular structure

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Multiple metal coordinating behaviour of the tetrapodal ligand 1,1,1,1-tetrakis[(salicylaldimino)methyl]methane

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Process for producing heterocyclic aldehyde

The present invention provides a process for preparing a heterocyclic aldehyde by oxidizing a heterocyclic alcohol with high selectivity and high yield. Specifically, the heterocyclic aldehyde is prepared by reacting a heterocyclic compound having at least one hydroxymethyl group bonded to a carbon atom of a heterocyclic ring with a hypohalogenous acid salt in the presence of a base to oxidize the hydroxymethyl group, wherein reaction is conducted in the co-presence of a 2,2,6,6-tetramethylpiperidine-1-oxyl derivative having at least two 2,2,6,6-tetramethylpiperidine-1-oxyl-4-yl groups.