Propanedioic acid,2,2-dibromo-, 1,3-diethyl ester
Propanedioic acid,2,2-dibromo-, 1,3-diethyl ester structure
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Common Name | Propanedioic acid,2,2-dibromo-, 1,3-diethyl ester | ||
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| CAS Number | 631-22-1 | Molecular Weight | 317.96000 | |
| Density | 1.68 | Boiling Point | 108ºC(4 torr) | |
| Molecular Formula | C7H10Br2O4 | Melting Point | N/A | |
| MSDS | Chinese USA | Flash Point | >230 °F | |
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Reductive and brominative termination of alkenol cyclization in aerobic cobalt-catalyzed reactions.
J. Am. Chem. Soc. 131(36) , 12918-20, (2009) Tetrahydrofur-2-ylmethyl radicals were stereoselectively generated from substituted pent-4-en-1-ols in aerobic cobalt(II)-catalyzed oxidations. Intermediates were trapped with cyclohexa-1,4-diene, gamma-terpinene, BrCCl(3), diethyl dibromomalonate, or electro... |
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Investigations into the Bromination of Substituted Phenols using Diethyl Bromomalonate and Diethyl Dibromomalonate. Coumbarides GS, et al.
Bull. Chem. Soc. Jpn. 74(1) , 179-80, (2001)
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Reaction of diethyl dibromomalonate with methoxide: Evidence for a novel bromophilic attack. Mebane RC, et al.
Tetrahedron Lett. 40(8) , 1459-62, (1999)
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A novel bromination for an unsaturated a-anion ester. Synthesis of 2-bromo-cis-8, cis-11, cis-14-eicosatrienoic acid. van der Wolf L and Pabon HJJ.
Rec. Trav. Chim. 96(3) , 72-74, (1977)
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Reactions of organocobalt complexes with bromoesters: regiospecific synthesis of allyl-and cyclopropylmethyl-substituted malonic and acetoacetic esters. Veber M, et al.
J. Organomet. Chem. 209(3) , 393-99, (1981)
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