79206-94-3

Basic information

• Product Name: 4-(2-FURYLMETHYL)-1LAMBDA6,4-THIAZINANE-1,1-DIONE
• Synonyms: 4-(2-FURYLMETHYL)-1LAMBDA6,4-THIAZINANE-1,1-DIONE;4-(FURFURYL)THIOMORPHOLINE-1,1-DIOXIDE
• CAS NO: 79206-94-3
• Molecular Formula: C₉H₁₃NO₃S
• Molecular Weight: 215.27
• Mol File: 79206-94-3.mol
• Article Data: 1

Chemical Properties

• Boiling Point: 378.7°C at 760 mmHg
• Flash Point: 182.8°C
• Appearance: /
• Density: 1.303g/cm³
• Vapor Pressure: 6.17E-06mmHg at 25°C
• Refractive Index: 1.555
• CAS DataBase Reference: 4-(2-FURYLMETHYL)-1LAMBDA6,4-THIAZINANE-1,1-DIONE(CAS DataBase Reference)
• NIST Chemistry Reference: 4-(2-FURYLMETHYL)-1LAMBDA6,4-THIAZINANE-1,1-DIONE(79206-94-3)
• EPA Substance Registry System: 4-(2-FURYLMETHYL)-1LAMBDA6,4-THIAZINANE-1,1-DIONE(79206-94-3)

Safety Data

• Hazardous Substances Data: 79206-94-3(Hazardous Substances Data)

Usage

Description

4-(2-Furylmethyl)-1Lamb6,4-thiazinane-1,1-dione is a chemical compound that belongs to the thiazinane-1,1-dione family. It is composed of a furan ring attached to a thiazinane-1,1-dione core structure. 4-(2-FURYLMETHYL)-1LAMBDA6,4-THIAZINANE-1,1-DIONE has potential applications in the field of medicinal chemistry due to its diverse pharmacological properties.
Used in Medicinal Chemistry:
4-(2-Furylmethyl)-1Lamb6,4-thiazinane-1,1-dione is used as a building block for the synthesis of bioactive molecules. Its unique structure and potential biological activities make it an interesting chemical compound for further research and exploration.
Used in Pharmaceutical Development:
4-(2-Furylmethyl)-1Lamb6,4-thiazinane-1,1-dione is used as a starting material for the development of new pharmaceuticals. Its diverse pharmacological properties make it a promising candidate for creating innovative drugs to address various medical conditions.

InChI:InChI=1/C9H13NO3S/c11-14(12)6-3-10(4-7-14)8-9-2-1-5-13-9/h1-2,5H,3-4,6-8H2

Upstream product

• 107-61-9 1,4-oxathiane-4,4-dioxide 
• 617-89-0 furan-2-ylmethanamine 

Downstream Products

• 79207-38-8 4-Benzyl-4-furan-2-ylmethyl-1,1-dioxo-1λ⁶-thiomorpholin-4-ium; bromide 

Relevant articles and documents

Concerning the Reactivity of Unsubstituted and Alkyl Substituted Thiomorpholines, 5. On the Joint Action of Elementary Sulfur and Gaseous Ammonia on Ketones, 95

The syntheses of 4-amino-thiomorpholine-1,1-dioxide (12) and 4-hydroxy-thiomorpholine-1,1-dioxide (11) from 1,4-thioxane-1,1-dioxide (1) by pressureless reaction of 1 with hydrazine hydrate and hydroxylamine, resp. is described.In analogy various other N-substituted thiomorpholine-1,1-dioxides are obtained with prim. amines (2-8) and diamines (9,10). 12 condensates with aldehydes (14-24) and ketones (25-29); reaction of 12 with 1 gives N,N'-dithiomorpholine-1,1-dioxide (13).Acylation of 12 with monochlorides (30-35), dichlorides of dicarboxylic acids (36-40) and carbo xylic acid anhydrides (41-43) proceeds smoothly.Compounds 38-43 are cyclic imides.Isocyanates give with 12 the expected compounds 45-48. 12 reacts with chlorinated 1,3,5-triazines to compounds which can be purified only with difficulty (49-51).Quaternization of the N-substituted thiomorpholine-1,1-dioxides with benzylbromide (52,53) and methyliodide (54,55) is possible.Ethylenbromide reacts with 9 to give the bis quaternization product 56.Further reactions of thiomorpholine-1,1-dioxide (57) with sulfuryl chloride (58), bromo cyanide (59), allylic chloride (60), chloro acetonitrile (61) and trityl chloride (62) are described. 11 reacts with carboxylic acid chlorides (63-65) and iso-cyanates (66-70) to yield the expected compounds.Propylene oxide gives with 12 the addition product 71; sulfur dioxide is added to 11 to thiomorpholine-1,1-dioxide sulfonic acid (72). - Keywords: 4-Aminothiomorpholine-1,1-dioxide; 4-Hydroxy-thiomorpholine-1,1-dioxide; Reactivity; Synthesis.