62217-35-0

Basic information

• Product Name: Dimethyl 1,3-Benzodithiol-2-ylphosphonate
• Synonyms: Dimethyl 1,3-Benzodithiol-2-ylphosphonate;1,3-Benzodithiol-2-ylphosphonic Acid Dimethyl Ester 2-Dimethoxyphosphinyl-1,3-benzodithiole
• CAS NO: 62217-35-0
• Molecular Formula: C₉H₁₁O₃PS₂
• Molecular Weight: 262.285601
• Mol File: 62217-35-0.mol
• Article Data: 3

Chemical Properties

• Melting Point: 120.0 to 124.0 °C
• Boiling Point: 383.2±42.0 °C(Predicted)
• Appearance: /
• Density: 1.39±0.1 g/cm3(Predicted)
• Storage Temp.: 0-10°C
• CAS DataBase Reference: Dimethyl 1,3-Benzodithiol-2-ylphosphonate(CAS DataBase Reference)
• NIST Chemistry Reference: Dimethyl 1,3-Benzodithiol-2-ylphosphonate(62217-35-0)
• EPA Substance Registry System: Dimethyl 1,3-Benzodithiol-2-ylphosphonate(62217-35-0)

Safety Data

• Hazardous Substances Data: 62217-35-0(Hazardous Substances Data)

Usage

General Description

Dimethyl 1,3-Benzodithiol-2-ylphosphonate is a chemical compound with the molecular formula C6H7O2PS2. It is a phosphonate ester that contains a benzodithiol group, which gives it unique chemical properties. The compound is commonly used as a reagent in organic synthesis and as a building block for the production of various pharmaceuticals and agrochemicals. It is also used as a stabilizer and flame retardant in the production of plastics and polymers. However, it is important to handle this compound with caution as it can be toxic and harmful if not used properly.

Upstream product

• 121-45-9 phosphorous acid trimethyl ester 
• 57842-27-0 1,3-benzodithiol-2-ylium tetrafluoroborate 

Downstream Products

• 62217-28-1 2-cyclohexylidene-1,3-benzodithiole 
• 38300-94-6 2-benzylidene-benzo[1,3]dithiole 
• 110166-37-5 2-(1-Cyclohexyl-ethylidene)-benzo[1,3]dithiole 
• 110166-41-1 2-(4-tert-Butyl-cyclohexylidene)-benzo[1,3]dithiole 
• 115820-66-1 4,8-Bis-benzo[1,3]dithiol-2-ylidene-4H,8H-benzo[1,2-c;4,5-c']dithiophene 
• 148806-27-3 2-(2-Diethoxymethyl-4,5-dimethyl-cyclohexa-1,4-dienylmethylene)-benzo[1,3]dithiole 
• 148806-24-0 2-(2-Diethoxymethyl-cyclohexa-1,4-dienylmethylene)-benzo[1,3]dithiole 
• 126148-22-9 (6S,9R)-5,10-Bis-benzo[1,3]dithiol-2-ylidene-2,3-diphenyl-5,5a,6,9,9a,10-hexahydro-6,9-methano-benzo[g]quinoxaline 
• 110166-39-7 2-(1-Benzyl-2-phenyl-ethylidene)-benzo[1,3]dithiole 
• 148806-25-1 2-Benzo[1,3]dithiol-2-ylidenemethyl-cyclohexa-1,4-dienecarbaldehyde 
• 148806-28-4 2-Benzo[1,3]dithiol-2-ylidenemethyl-4,5-dimethyl-cyclohexa-1,4-dienecarbaldehyde 
• 1156544-15-8 2,2'-(1-phenylethane-1,2-diylidene)bis(1,3-benzodithiole) 

Relevant articles and documents

Synthesis of new functionalized compounds related to π-extended tetrathiafulvalenes with quinonoidal structures bearing a ferrocene moiety

A number of π-extended conjugated tetrathiafulvalene (TTF) analogues were synthesized as new π-donors, and their structures and physical properties were determined. UV/Vis spectra and cyclic voltammetry of the π-extended ferrocenyl donors were studied in comparison with ferrocene, ferrocenylquinone, and the parent donor. A three-electron redox behaviour was observed. The absorption spectrum of the new donor 16 showed a slight red-shift and a slight increase in intensity relative to the compared compounds.

Synthesis and photochromic behaviour of new dipyrrolylperfluorocyclopentenes

The synthesis of new photoswitchable dipyrrolylethenes having different π-conjugated chain lengths, employing Wittig-Horner reaction, Knoevenagel condensation, Suzuki palladium catalyzed cross-coupling or Sonogashira coupling, is reported. Their photochemical behaviour, and in particular, their thermal stability has been investigated upon continuous irradiation with light of appropriate wavelengths.