13702-09-5

Basic information

• Product Name: DIPROPARGYL SULFIDE
• Synonyms: DIPROPARGYL SULFIDE;Propargyl Sulfide
• CAS NO: 13702-09-5
• Molecular Formula: C₆H₆S
• Molecular Weight: 110.18
• Mol File: 13702-09-5.mol

Chemical Properties

• Boiling Point: 59°C/14mmHg(lit.)
• Appearance: /
• Refractive Index: 1.5190 to 1.5230
• CAS DataBase Reference: DIPROPARGYL SULFIDE(CAS DataBase Reference)
• NIST Chemistry Reference: DIPROPARGYL SULFIDE(13702-09-5)
• EPA Substance Registry System: DIPROPARGYL SULFIDE(13702-09-5)

Safety Data

• RIDADR: UN 1993 3/PG III
• HazardClass: 3
• PackingGroup: III
• Hazardous Substances Data: 13702-09-5(Hazardous Substances Data)

Usage

Uses

Used in Pharmaceutical Industry:
Dipropargyl sulfide is used as a key intermediate in the synthesis of pharmaceuticals for its ability to contribute to the development of new drugs with potential therapeutic applications.
Used in Organic Synthesis:
In the field of organic chemistry, dipropargyl sulfide serves as a valuable building block for the creation of complex organic molecules, facilitating the advancement of chemical research and innovation.
Used in Antimicrobial Applications:
Dipropargyl sulfide is utilized as an antimicrobial agent due to its potential to combat various microorganisms, making it a candidate for use in sanitizing products and treatments.
Used in Anticancer Research:
As an anticancer agent, dipropargyl sulfide is explored for its capacity to inhibit the growth of cancer cells, offering a promising avenue for cancer treatment development.
Used in Anti-inflammatory and Antifungal Applications:
Dipropargyl sulfide is employed in the treatment of inflammation and fungal infections, leveraging its properties to alleviate symptoms and treat affected areas effectively.

InChI:InChI=1S/C6H6S/c1-3-5-7-6-4-2/h1-2H,5-6H2

Upstream product

• 106-96-7 propargyl bromide 
• 624-65-7 2-propynyl chloride 
• 75-15-0 carbon disulfide 

Downstream Products

• 127793-16-2 1-Oxa-6-thia-3,8-cyclodecadiyne 
• 291-21-4 [1,3,5]trithiane 
• 536725-05-0 3-[4-(3-{3-[4-(3-hydroxy-prop-1-ynyl)-phenyl]-prop-2-ynylsulfanyl}-prop-1-ynyl)-phenyl]-prop-2-yn-1-ol 
• 536725-04-9 3-[3-(3-{3-[3-(3-hydroxy-prop-1-ynyl)-phenyl]-prop-2-ynylsulfanyl}-prop-1-ynyl)-phenyl]-prop-2-yn-1-ol 
• 536725-06-1 C₂₄H₁₆Br₂S 
• 536725-07-2 C₂₄H₁₆Br₂S 
• 150782-89-1 tert-Butyl-dimethyl-[4-methyl-1-(3-prop-2-ynylsulfanyl-prop-1-ynyl)-cyclohex-3-enyloxy]-silane 
• 150782-88-0 4-{3-[1-(tert-Butyl-dimethyl-silanyloxy)-4-methyl-cyclohex-3-enyl]-prop-2-ynylsulfanyl}-but-2-ynal 
• 53690-50-9 1,6-Dithia-3,8-cyclodecadiin 
• 1150634-49-3 ethyl 2-phenyl-2-(propargylthio)penta-3,4-dienoate 
• 1226910-53-7 C₁₄H₁₂S 

Relevant articles and documents

Preparation of Structurally and Electronically Diverse N → B-Ladder Boranes by [2 + 2 + 2] Cycloaddition

We report the synthesis of a series of eight N → B-ladder boranes through cobalt-mediated cyclotrimerization of (2-cyanophenyl)-dimesitylborane with different dialkynes. The resulting tetracoordinate boranes show variable electrochemical and optical prope

POLYFUNCTIONAL PROPARGYL COMPOUND AND OPTICAL COMPOSITION COMPRISING THE SAME

PROBLEM TO BE SOLVED: To provide a new monomer compound from which an optical material can be manufactured that has at least one improved characteristic in a high refractive index and a high glass transition temperature, and a composition for an optical material comprising the above compound. SOLUTION: The present invention discloses a polyfunctional propargyl compound represented by formula (1) below. In the formula, m represents an integer of 3 to 30; R1 represents an alkyl which may have one or more sulfide bonds in the chain, and the alkyl is substituted if necessary; and each RA is independently selected from the group consisting of a hydrogen atom, halogen, alkyl having 1 to 10 carbon atoms, substituted or unsubstituted phenyl, substituted or unsubstituted naphthyl, and silyl. SELECTED DRAWING: None COPYRIGHT: (C)2019,JPOandINPIT

POLYMERIZABLE COMPOSITION AND NOVEL ALKYNE COMPOUND

Provided is a polymerizable composition including an alkyne compound represented by the following general formula (1): wherein, in general formula (1), X1 and X2 represent a sulfur atom, an oxygen atom, or an NH group and may be the same or different from each other, Q represents an alkylene group having 1 or 2 carbon atoms, a carbonyl group, or a thiophenylene group in which one of carbon atoms is substituted by an antimony atom, R1 and R2 represent an alkylene group having 1 or 2 carbon atoms and may be the same or different from each other, and m and n each represent 0 or 1.

Aryne triggered [2,3]-sigmatropic rearrangement of allyl and propargyl thioethers

An efficient protocol for [2,3]-sigmatropic rearrangement of allyl and propargyl thioethers is reported. The key sulfonium ylide intermediate is in situ formed via S-arylation of arynes. This transition metal-free method allows for ready access to a wide

Reactions of HDDA-Derived Benzynes with Sulfides: Mechanism, Modes, and Three-Component Reactions

We report here reactions of alkyl sulfides with benzynes thermally generated by the hexadehydro-Diels-Alder (HDDA) cycloisomerization. The initially produced 1,3-betaine (o-sulfonium/aryl carbanion) undergoes intramolecular proton transfer to generate a more stable S-aryl sulfur ylide. This can react in various manners, including engaging weak acids (HA) in the reaction medium. This can produce transient ion pairs ArSR2+A- that proceed to the products ArSR + RA. When cyclic sulfides are used, A- opens the ring and is incorporated into the product, an outcome that constitutes a versatile, three-component coupling process.