924906-80-9

Basic information

• Product Name: 2-Propyn-1-ol, 3-(4-methoxyphenyl)-, 1-methanesulfonate
• CAS NO: 924906-80-9
• Molecular Formula: C11H12O4S
• Molecular Weight: 240.28
• Mol File: 924906-80-9.mol
• Article Data: 6

Chemical Properties

• CAS DataBase Reference: 2-Propyn-1-ol, 3-(4-methoxyphenyl)-, 1-methanesulfonate(CAS DataBase Reference)
• NIST Chemistry Reference: 2-Propyn-1-ol, 3-(4-methoxyphenyl)-, 1-methanesulfonate(924906-80-9)
• EPA Substance Registry System: 2-Propyn-1-ol, 3-(4-methoxyphenyl)-, 1-methanesulfonate(924906-80-9)

Safety Data

• Hazardous Substances Data: 924906-80-9(Hazardous Substances Data)

Upstream product

• 696-62-8 para-iodoanisole 
• 37614-59-8 4-(4-methoxyphenyl)prop-2-yn-1-ol 
• 124-63-0 methanesulfonyl chloride 

Downstream Products

• 1041791-80-3 1-(1-ethyl-1,2-propadienyl)-4-methoxybenzene 
• 1613190-45-6 methyl 2-(2-(3-(4-methoxyphenyl)prop-2-ynyl)-2,3,4,9-tetrahydro-1H-pyrido[3,4-b]indol-1-yl)acetate 
• 1352213-67-2 N-(3-(4-methoxyphenyl)prop-2-yn-1-yl)-4-methyl-N-(3-phenylprop-2-yn-1-yl)benzenesulfonamide 
• 1599470-65-1 1-benzyl-3-(6-methoxy-1,3-dihydronaphtho[2,3-c]furan-4-yl)-1H-indole 
• 1599470-64-0 C₂₈H₂₃NO₂ 
• 1599470-54-8 1-benzyl-3-(3-((3-(4-methoxyphenyl)prop-2-yn-1-yl)oxy)prop-1-yn-1-yl)-1H-indole 
• 1599470-67-3 5-(4-methoxyphenyl)-6,8-dihydrofuro[3,4-g]quinoline 
• 1599470-70-8 1-benzyl-8-(4-methoxyphenyl)-3a,5,7,8a-tetrahydro-1H-isobenzofuro[5,6-d]imidazole 
• 1599470-55-9 2-(3-(3-(4-methoxyphenyl)prop-2-ynyloxy)prop-1-ynyl)pyridine 
• 1599470-56-0 1-benzyl-4-(3-(3-(4-methoxyphenyl)prop-2-ynyloxy)prop-1-ynyl)-1H-imidazole 
• 1453164-27-6 1-(3-azidoprop-1-yn-1-yl)-4-methoxybenzene 
• 91350-53-7 2-amino-4-(4-methoxybenzyl)thiazole 
• 1190928-74-5 C₁₂H₁₄N₂OS 
• 924906-85-4 N-benzyl-N-(3-(4-methoxyphenyl)prop-2-ynyl)-2,2-dimethylhexa-3,4-dienamide 

Relevant articles and documents

Intercepting the Banert cascade with nucleophilic fluorine: Direct access to α-fluorinated: N H-1,2,3-triazoles

The treatment of propargylic azides with silver(i) fluoride in acetonitrile was found to yield α-fluorinated NH-1,2,3-triazoles via the Banert cascade. The reaction was regioselective and the products result from an initial [3,3] rearrangement. The reacti

Selectivity in Garratt-Braverman cyclization of aryl-/heteroaryl- substituted unsymmetrical bis-propargyl systems: Formal synthesis of 7′-desmethylkealiiquinone

Unsymmetrical bis-propargyl ethers and sulfonamides containing various combinations of aryl/heteroaryl substituents at the acetylene termini were synthesized, and their reactivity under basic conditions was studied. Moderate to high (chemo)selectivity was

Rhodium(I)-catalyzed allenic carbocyclization reaction affording δ- and ε-lactams

(Chemical Equation Presented) This letter extends the scope of the rhodium(I)-catalyzed allenic Alder-ene carbocyclization reaction to the preparation of δ- and ε-lactams from amides. A variety of allenic propiolamides were cycloisomerized to give a numbe