20461-89-6

Basic information

• Product Name: 1,3-DITHIANE-2-CARBOXYLIC ACID
• Synonyms: 1,3-DITHIANE-2-CARBOXYLIC ACID;Glyoxylic Acid Trimethylene Dithioacetal
• CAS NO: 20461-89-6
• Molecular Formula: C₅H₈O₂S₂
• Molecular Weight: 164.25
• Mol File: 20461-89-6.mol
• Article Data: 18

Chemical Properties

• Melting Point: 115-116 °C
• Boiling Point: 354.7 °C at 760 mmHg
• Flash Point: 168.3 °C
• Appearance: /
• Density: 1.395 g/cm³
• PKA: 2.79±0.20(Predicted)
• CAS DataBase Reference: 1,3-DITHIANE-2-CARBOXYLIC ACID(CAS DataBase Reference)
• NIST Chemistry Reference: 1,3-DITHIANE-2-CARBOXYLIC ACID(20461-89-6)
• EPA Substance Registry System: 1,3-DITHIANE-2-CARBOXYLIC ACID(20461-89-6)

Safety Data

• Hazardous Substances Data: 20461-89-6(Hazardous Substances Data)

Usage

General Description

1,3-Dithiane-2-carboxylic acid is a chemical compound with the molecular formula C6H10O2S2. It is a carboxylic acid derivative of dithiane, which contains a six-membered ring with two sulfur atoms. 1,3-DITHIANE-2-CARBOXYLIC ACID is mainly used as a building block in organic chemical synthesis, particularly in the preparation of pharmaceuticals and agrochemicals. It is known for its ability to protect aldehydes and ketones from oxidation, as well as its use in the synthesis of complex organic molecules. Additionally, 1,3-dithiane-2-carboxylic acid is used in the preparation of various sulfur-containing compounds and can also be used as a reagent in organic reactions. Overall, this compound has applications in the field of organic chemistry and plays a crucial role in the synthesis of diverse chemical compounds.

Upstream product

• 873411-73-5 3,7-dioxo-3λ⁴,7λ⁴-dithia-nonanedioic acid 
• 505-23-7 1,3 dithiane 
• 124-38-9 carbon dioxide 
• 109-80-8 1.3-propanedithiol 
• 6000-59-5 glyoxalic acid monohydrate 
• 20462-00-4 ethyl 1,3-dithiane-2-carboxylate 
• 563-96-2 2,2-dihydroxyacetic acid 
• 64-19-7 acetic acid 
• 5065-18-9 3,3'-<(propane-1,3-diyl)bis(thio)>bis 
• 924-44-7 glyoxylic acid ethyl ester 
• 105-53-3 diethyl malonate 
• 298-12-4 Glyoxilic acid 
• 57529-04-1 2-chloro-1,3-dithiane 

Downstream Products

• 58216-30-1 2,3-diphenyl-5,9-dithia-2-aza-spiro[3,5]nonan-1-one 
• 71535-43-8 2-Benzyl-<1.3>-dithian-2-carbonsaeure 

Relevant articles and documents

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Anodic oxidation of dithiane carboxylic acids: A rapid and mild way to access functionalized orthoesters

A new electrochemical methodology has been developed for the preparation of a wide variety of functionalized orthoesters under mild and green conditions from easily accessible dithiane derivatives. The new methodology also offers an unprecedented way to access tri(fluorinated) orthoesters, a class of compound that has never been studied before. This provides the community with a rapid and general method to prepare libraries of functionalized orthoesters from simple and readily available starting materials.

Substituted Oxopyridine Derivatives and Use Thereof in the Treatment of Cardiovascular Disorders

The invention relates to substituted oxopyridine derivatives and to processes for their preparation, and also to their use for preparing medicaments for the treatment and/or prophylaxis of diseases, in particular cardiovascular disorders, preferably thrombotic or thromboembolic disorders, and oedemas, and also ophthalmic disorders.