Sign In to View Organizational & Contract Pricing.
Select a Size
About This Item
Linear Formula:
CH3C≡CCH2Br
CAS Number:
Molecular Weight:
132.99
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
MDL number:
Beilstein/REAXYS Number:
605306
Assay:
≥98%
Form:
liquid
InChI
1S/C4H5Br/c1-2-3-4-5/h4H2,1H3
SMILES string
CC#CCBr
InChI key
LNNXOEHOXSYWLD-UHFFFAOYSA-N
assay
≥98%
form
liquid
Quality Level
refractive index
n20/D 1.508 (lit.)
bp
40-41 °C/20 mmHg (lit.)
density
1.519 g/mL at 25 °C (lit.)
functional group
alkyl halide, bromo
Related Categories
General description
1-Bromo-2-butyne is a propargyl bromide derivative. It is one of the constitutional isomer of bromo butyne. Its Br-loss threshold photoionization breakdown diagram has been analyzed to derive dissociative photoionization thresholds to C4H5+ production. It participates in the preparation of linagliptin.
Application
1-Bromo-2-butyne was used in the alkylation of L-tryptophan methyl ester. It was used as a source to generate CH3CCCH2 radicals to investigate the reaction kinetics of these radicals with NO and NO2.
It may be used in the synthesis of the following:
It may be used in the synthesis of the following:
- 4-butynyloxybenzene sulfonyl chloride
- mono-propargylated diene derivative
- isopropylbut-2-ynylamine
- allenylcyclobutanol derivatives
- allyl-[4-(but-2-ynyloxy)phenyl]sulfane
- allenylindium
- alkynyl alcohols
- axially chiral teranyl compounds
Exploited in the synthesis of axially chiral teranyl compounds.
Choose from one of the most recent versions:
Already Own This Product?
Find documentation for the products that you have recently purchased in the Document Library.
Exploring the functional space of thiiranes as gelatinase inhibitors using click chemistry.
Testero SA, et al.
ARKIVOC (Gainesville, FL, United States), 7, 221-236 (2011)
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)
A chemical synthesis of 11-methoxy mitragynine pseudoindoxyl featuring the interrupted Ugi reaction.
Jimin Kim et al.
Chemical science, 3(9), 2849-2852 (2013-07-24)
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 and a
Takanori Shibata et al.
Journal of the American Chemical Society, 126(27), 8382-8383 (2004-07-09)
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 enantio- (>99.5% ee) and diastereoselectivities (dl/meso = >95/5)
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 Journal of Organic Chemistry, 2008(14), 2423-2429 (2008)
Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.
Contact Technical Service