|Related Categories||Alkynes, Building Blocks, Chemical Synthesis, Organic Building Blocks, Terminal More...|
|density||0.926 g/mL at 25 °C(lit.)|
Alkynyl substrate used in a study of a palladium-catalyzed coupling with β-tetrionic acid bromide leading to alkynyl substituted furanones in good yield.1
Synthon for preparation of oxygen-containing heterocycles and protected esters of s-Hydroxy-L-isoleucine
5, 25, 100 g in glass bottle
Certificate of Analysis
Certificate of Origin
|Precautionary statements||P261-P305 + P351 + P338|
|Personal Protective Equipment||Eyeshields, Faceshields, full-face respirator (US), Gloves, multi-purpose combination respirator cartridge (US), type ABEK (EN14387) respirator filter|
|Hazard Codes (Europe)||Xi|
|Risk Statements (Europe)||10-36/37/38|
|Safety Statements (Europe)||26-36|
|RIDADR||UN 1986 3/PG 3|
|Flash Point(F)||96.8 °F|
|Flash Point(C)||36 °C|
Alkynes contain a highly versatile functional group that may be utilized for numerous reactions such as electrophilic additions of hydrogen, halogens, hydrogen halides, or water; metathesis; hydrobor...
Aldrich ChemFiles 2008, 8.1, 14.
Keywords: 1,3-Dipolar cycloaddition, Addition reactions, Building blocks, Click chemistry, Cycloadditions, Favorskii Reaction, Metathesis, Nucleophilic additions, Nucleophilic substitutions, Substitutions
Aldrich Chemistry lists over 600 alkyne building blocks, including a wide array of propargyl alcohols, acetylenic boron reagents, and halogenated substrates for cross-coupling. Additionally, many of ...
Keywords: Building blocks, Coupling reactions, Cross couplings
1. Tetrahedron Lett. 48, 105, (2007)
Kopf, Henning; Pietraszuk. et al. Organometallics 25(10), 2533-2546, (2006)
Aldrich MSDS 1, 335:A / Corp MSDS 1 (1), 653:A / FT-IR 2 (3), 4025:C / FT-IR 1 (2), 936:C / FT-NMR 1 (3), 509:B / IR-Spectra (3), 1435:D / IR-Spectra (2), 1253:C / NMR-Reference 2 (2), 953:D / RegBook 1 (2), 2699:N / Structure Index 1, 425:C:7 / Vapor Phase 3, 1585:C
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