135655-77-5

Basic information

• Product Name: 1,3-Dithiane, 2-(2,4-dimethoxyphenyl)-
• CAS NO: 135655-77-5
• Molecular Formula: C12H16O2S2
• Molecular Weight: 256.39
• Mol File: 135655-77-5.mol
• Article Data: 9

Chemical Properties

• CAS DataBase Reference: 1,3-Dithiane, 2-(2,4-dimethoxyphenyl)-(CAS DataBase Reference)
• NIST Chemistry Reference: 1,3-Dithiane, 2-(2,4-dimethoxyphenyl)-(135655-77-5)
• EPA Substance Registry System: 1,3-Dithiane, 2-(2,4-dimethoxyphenyl)-(135655-77-5)

Safety Data

• Hazardous Substances Data: 135655-77-5(Hazardous Substances Data)

Usage

Type of compound

Dithiane derivative

Structural features

Contains a dithiane ring and a 2,4-dimethoxyphenyl group

Common use

Building block in organic synthesis for creating complex molecules

Specific applications

Creation of pharmaceuticals and natural products

Protective function

Shields aldehydes and ketones from unwanted reactions during chemical synthesis

Additional applications

Materials science and polymer chemistry

Reactivity

Unique reactivity due to its structural features

Importance

Valuable compound with diverse applications in organic chemistry

Upstream product

• 109-80-8 1.3-propanedithiol 
• 613-45-6 2,4-Dimethoxybenzaldehyde 
• 173282-52-5 Acetic acid acetoxy-(2,4-dimethoxy-phenyl)-methyl ester 

Downstream Products

• 91763-35-8 1-(p-methylphenyl)-1-pentanol 
• 613-45-6 2,4-Dimethoxybenzaldehyde 

Relevant articles and documents

Nickel(II) chloride as an efficient and useful catalyst for chemoselective thioacetalization of aldehydes

A wide variety of acyclic and cyclic dithioacetals can be prepared chemoselectively from the corresponding aldehydes by employing a catalytic amount of nickel(II) chloride in dry CH2Cl2-MeOH (5:1) at room temperature in good yields.

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

Efficient method for thioacetalization of carbonyl compounds in the presence of a catalytic amount of benzyltriphenylphosphonium tribromide (BTPTB) under solvent-free conditions

A variety of carbonyl compounds have been successfully converted to the corresponding thioacetal derivatives in good to excellent yields on reaction of carbonyl compounds with 1,2-ethanedithiole, 1,3-propanedithiol, and ethylthiol in the presence of a cat