252263
1-Bromo-2-ethylbutane
97%
Synonym(s):
3-(Bromomethyl)pentane
Sign In to View Organizational & Contract Pricing.
Select a Size
About This Item
Linear Formula:
(C2H5)2CHCH2Br
CAS Number:
Molecular Weight:
165.07
NACRES:
NA.22
PubChem Substance ID:
UNSPSC Code:
12352100
EC Number:
223-302-6
MDL number:
Product Name
1-Bromo-2-ethylbutane, 97%
form
liquid
InChI key
KKGUMGWNFARLSL-UHFFFAOYSA-N
InChI
1S/C6H13Br/c1-3-6(4-2)5-7/h6H,3-5H2,1-2H3
SMILES string
CCC(CC)CBr
assay
97%
refractive index
n20/D 1.4498 (lit.)
bp
143-144 °C (lit.)
density
1.179 g/mL at 25 °C (lit.)
functional group
alkyl halide
bromo
Application
1-Bromo-2-ethylbutane was used in the preparation of dialkoxytriarylamine. It was also used as cysteine-modifying reagent.
Reactant involved in the synthesis of biologically active molecules including:
Reactant involved in studies of the effect of oxygenated side chains in Ephedra compounds
- Nantenine analogs with aporphinoid 5-HT2A and α-1A antagonistic activity
- Aporphines with cytotoxicity toward human colon cancer cell lines
- Dimeric amide foldamers acting as alpha-helix mimetics
- Endocrine-disrupting nanylphenol isomers synthesized via demethylation
- Phosphonic acid-containing benzimidazoles for use as fructose-1,6-biphosphatase inhibitors
- 5-Bromo-1H-indole-3-acetohydroxamic acid for use as peptide deformylase inhibitors
Reactant involved in studies of the effect of oxygenated side chains in Ephedra compounds
signalword
Warning
hcodes
Hazard Classifications
Flam. Liq. 3
Storage Class
3 - Flammable liquids
wgk
WGK 3
flash_point_f
96.8 °F - closed cup
flash_point_c
36 °C - closed cup
ppe
Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter
Regulatory Information
新产品
This item has
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.
Enhanced poling efficiency in highly thermal and photostable nonlinear optical chromophores.
Faccini M, et al.
Journal of Materials Chemistry, 18(18), 2141-2149 (2008)
Usama M Hegazy et al.
Chemistry & biology, 13(9), 929-936 (2006-09-21)
Proteins contain amino acid residues essential to structure and function. Ribosomal protein synthesis is typically limited to the 20 amino acids of the genetic code, but posttranslational chemical modifications can greatly expand the diversity of side chain functionalities. In this
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