16602
Methyl 2-bromohexanoate
≥99.0% (GC)
Synonym(s):
Methyl 2-bromocaproate
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About This Item
Linear Formula:
CH3(CH2)3CHBrCOOCH3
CAS Number:
Molecular Weight:
209.08
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
226-643-9
Beilstein/REAXYS Number:
1722052
MDL number:
Assay:
≥99.0% (GC)
InChI key
YGLPDRIMFIXNBI-UHFFFAOYSA-N
InChI
1S/C7H13BrO2/c1-3-4-5-6(8)7(9)10-2/h6H,3-5H2,1-2H3
SMILES string
CCCCC(Br)C(=O)OC
assay
≥99.0% (GC)
refractive index
n20/D 1.455
density
1.289 g/mL at 20 °C (lit.)
functional group
bromo, ester
General description
Methyl 2-bromohexanoate undergoes addition reaction with methyl-10-undecenoate to yield lactone and dimethyl-2-butyltridecandioate.
Application
Methyl 2-bromohexanoate was used in the synthesis of 2-butyl-2H-pyrido[3,2-b]-1,4-oxazin-3(4H)-one.
Storage Class
10 - Combustible liquids
wgk
WGK 3
flash_point_f
156.2 °F - closed cup
flash_point_c
69 °C - closed cup
ppe
Eyeshields, Gloves, type ABEK (EN14387) respirator filter
Regulatory Information
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Preparation of 2H-Pyrido [3, 2-b]-l,4-oxazin-3 (4H)-ones and of the Corresponding Dihydropyridooxazines.
Clauson-Kaas NIELS, et al.
Acta Chemica Scandinavica, 23(7), 2322-2324 (1969)
Radical Additions of Alkyl 2-Haloalkanoates and 2-Haloalkanenitriles to Alkenes Initiated by Electron Transfer from Copper in Solvent-Free Systems.
Metzger JO, et al.
European Journal of Organic Chemistry, 1997(11), 2303-2313 (1997)
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