23229-29-0

Basic information

• Product Name: 4-Methylbenzaldehyde ethane-1,2-diyl dithioacetal
• Synonyms: 2-(4-Methylphenyl)-1,3-dithiolane;2-(p-Tolyl)-1,3-dithiolane;4-Methylbenzaldehyde (ethane-1,2-diyl)dithioacetal;4-Methylbenzaldehyde ethane-1,2-diyl dithioacetal
• CAS NO: 23229-29-0
• Molecular Formula: C₁₀H₁₂S₂
• Molecular Weight: 196.3323
• Mol File: 23229-29-0.mol
• Article Data: 56

Chemical Properties

• Boiling Point: 325.4°Cat760mmHg
• Flash Point: 157.2°C
• Appearance: /
• Density: 1.167g/cm³
• Vapor Pressure: 0.000437mmHg at 25°C
• Refractive Index: 1.624
• CAS DataBase Reference: 4-Methylbenzaldehyde ethane-1,2-diyl dithioacetal(CAS DataBase Reference)
• NIST Chemistry Reference: 4-Methylbenzaldehyde ethane-1,2-diyl dithioacetal(23229-29-0)
• EPA Substance Registry System: 4-Methylbenzaldehyde ethane-1,2-diyl dithioacetal(23229-29-0)

Safety Data

• Hazardous Substances Data: 23229-29-0(Hazardous Substances Data)

Usage

InChI:InChI=1/C10H12S2/c1-8-2-4-9(5-3-8)10-11-6-7-12-10/h2-5,10H,6-7H2,1H3

Upstream product

• 104-87-0 4-methyl-benzaldehyde 
• 540-63-6 ethane-1,2-dithiol 
• 2403-51-2 2-(4-methylphenyl)-1,3-dioxolane 
• 1900-85-2 phenyl p-methylbenzoate 
• 874-60-2 4-methyl-benzoyl chloride 
• 99-75-2 4-methyl-benzoic acid methyl ester 
• 99-94-5 p-Toluic acid 
• 2929-93-3 p-tolylmethylenediacetate 
• 5663-40-1 2-(4-methylphenyl)-1,3-dioxane 
• 53731-74-1 3,9-di-p-tolyl-2,4,8,10-tetraoxa-spiro[5.5]undecane 
• 22391-04-4 2-(4-tolyl)-1,3-oxathiolane 

Downstream Products

• 22975-58-2 1-methyl-4-(1'-ethyl)propylbenzene 
• 20849-31-4 4-Methyldithiobenzoesaeurephenylester 
• 1822-73-7 phenylthioethylene 
• 104-87-0 4-methyl-benzaldehyde 
• 94-08-6 4-methylbenzoic acid ethyl ester 
• 106-42-3 para-xylene 

Relevant articles and documents

A facile and efficient procedure for the transdithioacetalization of 1,1-diacetates using POCl3-montmorillonite as catalyst

A rapid and efficient method for the transdithioacetalization of 1,1-diacetates with 1,2-dithioglycol was described in good to excellent yield catalyzed by POCl3-montmorillonite.

One-pot two-step conversion of aromatic carboxylic acids and esters to aromatic aldehydes via indium-catalyzed reductive thioacetalization and desulfurization

Described herein is that a new approach to a one-pot two-step conversion of aromatic carboxylic acids/esters to aromatic aldehydes, in which indium(III) iodide effectively catalyzes both the first reductive thioacetalization of carboxylic acids and a subsequent desulfurization of the in-situ formed thioacetal intermediates leading to aldehydes.

Sulfonated polyanthracene-catalyzed highly efficient and chemoselective thioacetalization of carbonyl compounds and transthioacetalization of acetals and acylals

A straightforward and highly efficient procedure for the thioacetalization of a variety of aldehydes and transthioacetalization of acylals and acetals in good to excellent yields using catalytic amounts of sulfonated polyanthracene (S-PAT) is reported. Th