124700-26-1

Basic information

• Product Name: Benzene, 1-fluoro-4-(2-propynyloxy)- (9CI)
• Synonyms: Benzene, 1-fluoro-4-(2-propynyloxy)- (9CI);4-Fluoro-phenyl propargyl ether;1-FLUORO-4-(PROP-2-YN-1-YLOXY)BENZENE(WXFC0574)
• CAS NO: 124700-26-1
• Molecular Formula: C₉H₇FO
• Molecular Weight: 150.1496832
• Product Categories: METHOXY
• Mol File: 124700-26-1.mol
• Article Data: 31

Chemical Properties

• Boiling Point: 218.9±20.0 °C(Predicted)
• Appearance: /
• Density: 1.116±0.06 g/cm3(Predicted)
• CAS DataBase Reference: Benzene, 1-fluoro-4-(2-propynyloxy)- (9CI)(CAS DataBase Reference)
• NIST Chemistry Reference: Benzene, 1-fluoro-4-(2-propynyloxy)- (9CI)(124700-26-1)
• EPA Substance Registry System: Benzene, 1-fluoro-4-(2-propynyloxy)- (9CI)(124700-26-1)

Safety Data

• Hazardous Substances Data: 124700-26-1(Hazardous Substances Data)

Upstream product

• 371-41-5 4-Fluorophenol 
• 6921-27-3 dipropargyl ether 
• 107-19-7 propargyl alcohol 
• 2003-82-9 3-bromo-2-propyne 
• 106-96-7 propargyl bromide 

Downstream Products

• 1292210-26-4 1-(2,2-difluoro-2-(phenylthio)ethyl)-4-((4-fluorophenoxy)methyl)-1H-1,2,3-triazole 
• 1292210-40-2 1-(2,2-difluoroethyl)-4-((4-fluorophenoxy)methyl)-1H-1,2,3-triazole 
• 305805-92-9 (2Z)-4-(4-fluorophenoxy)-3-iodo-1-(3,4,5-trimethoxyphenyl)but-2-en-1-one 
• 305806-02-4 (2Z)-4-(4-fluorophenoxy)-3-iodo-1-(3,4,5-trimethoxyphenyl)but-2-en-1-ol 
• 305805-87-2 (3Z)-4-(4-fluorophenoxy)-3-iodo-1-(3,4,5-trimethoxyphenyl)but-3-en-1-one 
• 305805-97-4 (3Z)-4-(4-fluorophenoxy)-3-iodo-1-(3,4,5-trimethoxyphenyl)but-3-en-1-ol 
• 305805-82-7 4-(4-fluorophenoxy)-1-(3,4,5-trimethoxyphenyl)but-2-yn-1-one 
• 305805-85-0 (4Z)-5-(4-fluorophenoxy)-4-iodopent-4-en-2-one 
• 305805-95-2 (4Z)-5-(4-fluorophenoxy)-4-iodopent-4-en-2-ol 
• 305805-90-7 (3Z)-5-(4-fluorophenoxy)-4-iodopent-3-en-2-one 
• 305806-00-2 (3Z)-5-(4-fluorophenoxy)-4-iodopent-3-en-2-ol 
• 305805-80-5 5-(4-fluorophenoxy)pent-3-yn-2-one 
• 371-41-5 4-Fluorophenol 
• 305805-77-0 5-(4-fluorophenoxy)pent-3-yn-2-ol 

Relevant articles and documents

1,2,3-Triazole-based kojic acid analogs as potent tyrosinase inhibitors: Design, synthesis and biological evaluation

A series of kojic acid-derived compounds 6a-p bearing aryloxymethyl-1H-1,2,3-triazol-1-yl moiety were designed by modifying primary alcoholic group of kojic acid as tyrosinase inhibitors. The target compounds 6a-p were synthesized via click reaction. All

Compound of dipyrrolopyridine structure Preparation method and medical application

The invention discloses a compound with a dipyrrolo-pyridine structure as well as a preparation method and medical application thereof. The compound provided by the invention has obvious inhibitory activity on JAK family proteins, is an effective JAK inhibitor, and has the prospect of being developed into drugs for inhibiting JAK and further treating diseases.

Enantioselective Palladium-Catalyzed Hydrophosphinylation of Allenes with Phosphine Oxides: Access to Chiral Allylic Phosphine Oxides

A Pd-catalyzed hydrophosphinylation of alkyl and aryl-oxyallenes with phosphine oxides has been developed for the efficient and rapid construction of a family of chiral allylic phosphine oxides with a diverse range of functional groups. This methodology was further applied in the facile construction of chiral 2H-chromene and later stage functionalization of cholesterol.

Synthesis, characterization, and antiplasmodial efficacy of sulfonamide-appended [1,2,3]-triazoles

A series of benzenesulfonamide-appended [1,2,3]-triazole hybrids was synthesized by using [3 + 2] cycloaddition of primary, secondary, and tertiary sulfonamide azides with various phenoxymethylacetylenes under click reaction conditions. After structural c