Sign In to View Organizational & Contract Pricing.
Select a Size
Change View
About This Item
Linear Formula:
CH3CH2CHBrCH3
CAS Number:
Molecular Weight:
137.02
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
201-140-7
Beilstein/REAXYS Number:
505949
MDL number:
Assay:
98%
Form:
liquid
Quality Level
assay
98%
form
liquid
refractive index
n20/D 1.437 (lit.)
bp
91 °C (lit.)
density
1.255 g/mL at 25 °C (lit.)
SMILES string
CCC(C)Br
InChI
1S/C4H9Br/c1-3-4(2)5/h4H,3H2,1-2H3
InChI key
UPSXAPQYNGXVBF-UHFFFAOYSA-N
General description
Viscosities of binary mixtures of 2-bromobutane and the isomeric forms of butanol have been evaluated at 298.15 and 313.15K. 2,2-dibromobutane, meso-2,3-dibromobutane and dl-2,3-dibromobutane are formed as major photobromination reaction products, during its reaction with molecular bromine. Smaller yields of 1,2-dibromobutane and 2,2,3-tribromobutane are also obtained in this reaction.
2-Bromobutane is an alkyl halide. Degradation of 2-bromobutane by reductive dehalogenation in the presence of nickel-aluminum alloy in potassium hydroxide solution has been reported. Gas chromatographic determination of 2-bromobutane in mixture of alkyl bromides has been reported. Stereochemistry of dehydrobromination of 2-bromobutane over KOH-silica has been investigated.
Application
2-Bromobutane may be used in the synthesis of series of non-nucleosides.
signalword
Danger
hcodes
Hazard Classifications
Aquatic Chronic 3 - Flam. Liq. 2
Storage Class
3 - Flammable liquids
wgk
WGK 2
flash_point_f
69.8 °F - closed cup
flash_point_c
21 °C - closed cup
ppe
Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter
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.
Photobromination of (-)-(2R)-2-bromobutane with bromine-81.
Tanner DD, et al.
Journal of the American Chemical Society, 99(8), 2714-2723 (1977)
Khalid Mohammed Hassan Hilmy
Archiv der Pharmazie, 339(4), 174-181 (2006-04-06)
A series of non-nucleosides 9-47 were synthesized. Compounds 1-4 were reacted with formic acid (85%) to afford compounds 5-8. Then, the latter compounds were reacted with alkyl halides a-f (2-bromopropane, 2-bromobutane, benzyl bromide, benzyl chloromethyl ether, chloromethyl ethyl ether, phenacyl
STEREOCHEMISTRY AND ISOTOPE EFFECT IN THE DEHYDROBROMINATION OF 2-BROMOBUTANE OVER SOLID CATALYSTS.
Misono M and Yoneda Y.
Chemistry Letters (Jpn), 1(7), 551-552 (1972)
Global Trade Item Number
| SKU | GTIN |
|---|---|
| B59500-500G | 04061833434376 |
| B59500-100G | 04061833434369 |
