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
Beilstein:
1722052
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22
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Assay
≥99.0% (GC)
refractive index
n20/D 1.455
density
1.289 g/mL at 20 °C (lit.)
functional group
bromo
ester
SMILES string
CCCCC(Br)C(=O)OC
InChI
1S/C7H13BrO2/c1-3-4-5-6(8)7(9)10-2/h6H,3-5H2,1-2H3
InChI key
YGLPDRIMFIXNBI-UHFFFAOYSA-N
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 Code
10 - Combustible liquids
WGK
WGK 3
Flash Point(F)
156.2 °F - closed cup
Flash Point(C)
69 °C - closed cup
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
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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)
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)
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