CAS 149506-35-4
:Propanedioic acid, 2-(4-bromophenyl)-, 1,3-dimethyl ester
Description:
Propanedioic acid, 2-(4-bromophenyl)-, 1,3-dimethyl ester, also known by its CAS number 149506-35-4, is an organic compound characterized by its structure, which includes a propanedioic acid backbone with two methyl ester groups and a para-bromophenyl substituent. This compound typically exhibits properties associated with esters, such as being a colorless to pale yellow liquid or solid, depending on its specific form and purity. It is likely to be soluble in organic solvents due to the presence of the ester functional groups, while its solubility in water may be limited. The presence of the bromophenyl group can impart unique reactivity, making it a potential candidate for various chemical reactions, including nucleophilic substitutions and coupling reactions. Additionally, the compound may exhibit biological activity, which could be of interest in pharmaceutical applications. As with many organic compounds, handling should be done with care, considering potential toxicity and environmental impact.
Formula:C11H11BrO4
InChI:InChI=1S/C11H11BrO4/c1-15-10(13)9(11(14)16-2)7-3-5-8(12)6-4-7/h3-6,9H,1-2H3
InChI key:InChIKey=UODIEONWLZBSEK-UHFFFAOYSA-N
SMILES:C(C(OC)=O)(C(OC)=O)C1=CC=C(Br)C=C1
Synonyms:- 1,3-Dimethyl 2-(4-bromophenyl)propanedioate
- 2-(4-Bromo-phenyl)-malonic acid dimethyl ester
- 2-(4-Bromophenyl)malonic acid dimethyl ester
- Dimethyl (4-bromophenyl)malonate
- Dimethyl 2-(4-bromophenyl)propanedioate
- Propanedioic acid, (4-bromophenyl)-, dimethyl ester
- Propanedioic acid,2-(4-bromophenyl)-, 1,3-dimethyl ester
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Found 6 products.
1,3-Dimethyl 2-(4-bromophenyl)propanedioate
CAS:Formula:C11H11BrO4Purity:98%Color and Shape:SolidMolecular weight:287.1066Dimethyl 2-(4-bromophenyl)malonate
CAS:Dimethyl 2-(4-bromophenyl)malonatePurity:98%Molecular weight:287.11g/mol1,3-dimethyl 2-(4-bromophenyl)propanedioate
CAS:1,3-dimethyl 2-(4-bromophenyl)propanedioate is a versatile compound with various applications. It has been used as an intermediate in the synthesis of indole-3-acetic acid and dasatinib. Mass spectrometric methods have been employed to analyze the compound's structure and purity. Additionally, it has been studied for its interactions with biomolecules such as histidine and ubiquitin ligases. This compound also exhibits antimicrobial properties, making it a potential candidate for the development of new antimicrobial agents. Researchers have also explored its use in calmodulin-based electrode systems and its ability to modify hydroxyl groups on other compounds. With its wide range of applications, 1,3-dimethyl 2-(4-bromophenyl)propanedioate holds promise as a valuable research chemical in various fields including medicine, chemistry, and biotechnology.Formula:C11H11BrO4Purity:Min. 95%Molecular weight:287.11 g/mol





