1-Bromo-2-butyne
1-Bromo-2-butyne structure
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Common Name | 1-Bromo-2-butyne | ||
|---|---|---|---|---|
| CAS Number | 3355-28-0 | Molecular Weight | 132.986 | |
| Density | 1.5±0.1 g/cm3 | Boiling Point | 124.7±23.0 °C at 760 mmHg | |
| Molecular Formula | C4H5Br | Melting Point | N/A | |
| MSDS | Chinese USA | Flash Point | 36.3±17.0 °C | |
| Symbol |
GHS02 |
Signal Word | Warning | |
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A chemical synthesis of 11-methoxy mitragynine pseudoindoxyl featuring the interrupted Ugi reaction.
Chem. Sci. 3(9) , 2849-2852, (2012) A synthesis of 11-methoxy mitragynine pseudoindoxyl, a new member of the mitragynine class of opioid agonists, from a derivative of the Geissman-Waiss lactone is described. An internal attack of an electron-rich aromatic ring on an electrophilic nitrilium ion... |
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Iridium complex-catalyzed highly enantio- and diastereoselective [2+2+2] cycloaddition for the synthesis of axially chiral teraryl compounds.
J. Am. Chem. Soc. 126(27) , 8382-8383, (2004) An asymmetric [2+2+2] cycloaddition of an alpha,omega-diyne, possessing ortho-substituted aryl groups on its terminus, and a monoalkyne with oxygen functionalities gave various axially chiral teraryl compounds. The coupling proceeded with extremely high enant... |
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Imaging breakdown diagrams for bromobutyne isomers with photoelectron-photoion coincidence. Bodi A and Hemberger P.
Phys. Chem. Chem. Phys. 16(2) , 505-515, (2014)
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Facile Entry to 4, 5, 6, 7-Tetrahydro [1, 2, 3] triazolo [1, 5-a] pyrazin-6-ones from Amines and Amino Acids. Sai SV, et al.
European J. Org. Chem. 2008(14) , 2423-2429, (2008)
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Acetylenic TACE inhibitors. Part 1. SAR of the acyclic sulfonamide hydroxamates. Levin JI, et al.
Bioorg. Med. Chem. Lett. 13(16) , 2799-2803, (2003)
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Reaction of zirconacyclopentadienes with electrophiles such as benzaldehyde, methyl methacrylate and 1-bromo-2-butyne after treatment with RLi. Seki T, et al.
Tetrahedron Lett. 45(49) , 9041-9043, (2004)
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Strained, Stable 2-Aza-1-Phosphabicyclo [n.1.0] alkane and-alkene Fe(CO)4 Complexes with Dynamic Phosphinidene Behavior. Borst MLG, et al.
Chemistry 11(12) , 3631-3642, (2005)
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Stereoselective synthesis of a-disubstituted cyclopentanones by palladium-catalyzed rearrangement of allenylcyclobutanols with aryl halides. Yoshida M, et al.
Tetrahedron 58(39) , 7839-7846, (2002)
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Exploring the functional space of thiiranes as gelatinase inhibitors using click chemistry. Testero SA, et al.
ARKIVOC 7 , 221-36, (2011)
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Synthesis of Cyclic Compounds Having exo-Methylene Groups through the Diels-Alder Reactions of Vinyl Allenes Obtained from Propargyl Bromide and Indium. Lee K and Lee PH.
Bull. Korean Chem. Soc. 29(2) , 487, (2008)
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