6007-22-3

Basic information

• Product Name: 2,2-Dimethyl-1,3-dithiane
• Synonyms: 2,2-Dimethyl-1,3-dithiane
• CAS NO: 6007-22-3
• Molecular Formula: C₆H₁₂S₂
• Molecular Weight: 148.29
• Mol File: 6007-22-3.mol
• Article Data: 8

Chemical Properties

• Appearance: /
• CAS DataBase Reference: 2,2-Dimethyl-1,3-dithiane(CAS DataBase Reference)
• NIST Chemistry Reference: 2,2-Dimethyl-1,3-dithiane(6007-22-3)
• EPA Substance Registry System: 2,2-Dimethyl-1,3-dithiane(6007-22-3)

Safety Data

• Hazardous Substances Data: 6007-22-3(Hazardous Substances Data)

Usage

Physical state

A colorless liquid.

Odor

Strong and unpleasant.

Usage

Primarily used as a reagent in organic synthesis.

Applications

As a building block in the preparation of various organic compounds, including pharmaceuticals, agrochemicals, and fine chemicals; as a protecting group for aldehydes and ketones in organic synthesis; as a reagent for the synthesis of complex molecules; and as a source of sulfur in organic reactions.

Hazards

Flammable and may cause irritation to the skin, eyes, and respiratory tract, and should be handled with care.

Upstream product

• 540-63-6 ethane-1,2-dithiol 
• 67-64-1 acetone 
• 109-80-8 1.3-propanedithiol 
• 77-76-9 2,2-dimethoxy-propane 
• 83141-42-8 2-(2,2-dimethyl-1,3-dioxolan-4-yl)acetaldehyde 
• 32233-44-6 2-[(4S)-2,2-dimethyl-1,3-dioxolan-4-yl]acetaldehyde 

Downstream Products

• 79032-16-9 1,2-dithiolane 1-oxide 
• 67-64-1 acetone 
• 87441-49-4 (-)-(1S)-2,2-dimethyl-1,3-dithian 1-oxide 
• 619326-29-3 (R)-2,2-dimethyl-1,3-dithiane-1-oxide 
• 41893-06-5 2,2-dimethyl-1,3-dithiane-1-oxide 

Relevant articles and documents

Novel sulphone-containing lithium ion battery electrolyte additive and preparation and application thereof

The invention discloses a novel sulphone-containing lithium ion battery electrolyte additive and preparation and application thereof, and belongs to the field of electrolyte additives. The lithium ionbattery electrolyte additive is an organic sulfone comp

Effect of β-alkylthioethyl substitution in 1,3-dithianes: Quasianchimeric assistance in photoinduced electron transfer?

(Figure Presented) Nanosecond laser flash photolysis (LFP) experiments show that the rates of ET quenching of triplet benzophenone by 2-alkyldithianes significantly decrease with bulkier substitution. Introduction of sulfur at the β-position of the flexib

Transdithioacetalization of acetals, ketals, oximes, enamines and tosylhydrazones catalysed by natural kaolinitic clay

Natural kaolinitic clay efficiently catalyses the transdithioacetalization of acetals, ketals, oximes, enamines and tosylhydrazones with ethane-1,2-dithiol and propane-1,3-dithiol to produce the corresponding dithiolanes in high yields.