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
• Article Data: 7

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

General Description

Dipropargyl sulfide is a chemical compound with the molecular formula C6H8S. It is a colorless to pale yellow liquid with a strong garlic-like odor. It is commonly used in the synthesis of organic compounds and pharmaceuticals. Dipropargyl sulfide is also known for its potential antimicrobial and anticancer properties. It has been studied for its use in the treatment of various medical conditions, including as an anti-inflammatory and antifungal agent. However,

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

Upstream product

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

Downstream Products

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

Relevant articles and documents

Reaction of bis(prop-2-yn-1-yl) sulfide with sulfur dichloride. First example of cyclization of bis(prop-2-yn-1-yl) chalcogenides by the action of chalcogen halides

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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

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