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CAS 4513-62-6

:

1,6-Dimethyl 2-methyl-5-methylenehexanedioate

Description:
1,6-Dimethyl 2-methyl-5-methylenehexanedioate, with the CAS number 4513-62-6, is an organic compound characterized by its diester functional groups. This substance features a hexanedioate backbone, which indicates the presence of two carboxylate groups, each esterified with methyl groups. The presence of multiple methyl groups contributes to its branched structure, influencing its physical and chemical properties, such as boiling point, solubility, and reactivity. Typically, compounds of this nature are colorless to pale yellow liquids or solids, depending on their purity and specific structural characteristics. They may exhibit moderate volatility and are often soluble in organic solvents. The compound's reactivity can be attributed to the ester functional groups, making it a potential candidate for various chemical reactions, including hydrolysis and transesterification. Additionally, its branched structure may impart unique properties, such as lower melting points compared to linear analogs. Overall, 1,6-Dimethyl 2-methyl-5-methylenehexanedioate is of interest in organic synthesis and may have applications in the production of polymers or other chemical intermediates.
Formula:C10H16O4
InChI:InChI=1S/C10H16O4/c1-7(9(11)13-3)5-6-8(2)10(12)14-4/h8H,1,5-6H2,2-4H3
InChI key:InChIKey=SUISJNPVANLQPB-UHFFFAOYSA-N
SMILES:C(C(OC)=O)(CCC(C(OC)=O)=C)C
Synonyms:
  • 1,6-Dimethyl 2-methyl-5-methylenehexanedioate
  • 1,6-Dimethyl 2-methyl-5-methylidenehexanedioate
  • Dimethyl 1-hexene-2,5-dicarboxylate
  • Dimethyl 2-Methyl-5-Methylidenehexanedioate
  • Dimethyl 2-methyl-5-methylenehexanedioate
  • Dimethyl 2-methylene-5-methyladipate
  • Hexanedioic acid, 2-methyl-5-methylene-, 1,6-dimethyl ester
  • Hexanedioic acid, 2-methyl-5-methylene-, dimethyl ester
  • Dimethyl 2-methyl-5-methyleneadipate
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