34310
Methyl 2,3-dibromopropionate
≥97.0% (GC)
Sign Into View Organizational & Contract Pricing
Select a Size
About This Item
Linear Formula:
CH2BrCHBrCOOCH3
CAS Number:
Molecular Weight:
245.90
Beilstein:
1750190
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22
Assay
≥97.0% (GC)
form
liquid
refractive index
n20/D 1.514
bp
83-86 °C/10 mmHg (lit.)
density
1.944 g/mL at 20 °C (lit.)
storage temp.
2-8°C
SMILES string
COC(=O)C(Br)CBr
InChI
1S/C4H6Br2O2/c1-8-4(7)3(6)2-5/h3H,2H2,1H3
InChI key
ROXQOUUAPQUMLN-UHFFFAOYSA-N
Looking for similar products? Visit Product Comparison Guide
General description
Methyl 2,3-dibromopropionate is the methyl ester of 2,3-dibromopropanoic acid. It reacts with 2-acetamido-3-hydroxypyridine to give 2-substituted pyrido-oxazine.
Application
Methyl 2,3-dibromopropionate may be used in the preparation of methyl 2-azidoacrylate. It may be used in the preparation of methyl (+)-(1′R, 2R) and (-)-(1′R, 2S)-1-(2-phenylethanol)aziridine-2-carboxylates.
Signal Word
Warning
Hazard Statements
Precautionary Statements
Hazard Classifications
Eye Irrit. 2 - STOT SE 3
Target Organs
Respiratory system
Storage Class Code
10 - Combustible liquids
WGK
WGK 3
Flash Point(F)
Not applicable
Flash Point(C)
Not applicable
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
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.
Regiospecific and Enantiospecific Ring Opening of Methyl (+)-(1'R, 2R)-and (-)-(1'R, 2S)-1-(2-phenylethanol) Aziridine-2-carboxylates.
Gnecco D, et al.
Molecules (Basel), 5(8), 998-1003 (2000)
2H-Azirines as dipolarophiles.
Pinho e Melo TMVD, et al.
Tetrahedron Letters, 44(33), 6313-6315 (2003)
Synthesis of substituted 3, 4-dihydro-2< i> H</i>-pyrido [3, 2-< i> b</i>][1, 4] oxazine as new scaffolds for potential bioactive compounds.
Henry N, et al.
Tetrahedron, 62(10), 2405-2412 (2006)
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