What is the structure of 2 methylbutanoic acid?
What is the structure of 2 methylbutanoic acid?
C5H10O2
2-Methylbutanoic acid/Formula
Is 2 methylbutanoic acid chiral?
… an example, consider 2-hydroxy-2-methylbutanoic acid shown in Figure 1. The a-carbon is chiral, and thus this molecule has two mirror-image structures. … can occur when connections to the double-bonded atoms are terminal atoms rather than structural fragments.
Is 2 methylbutanoic acid soluble in water?
Belongs to the class of organic compounds known as methyl-branched fatty acids….Structure for FDB008135 (2-Methylbutanoic acid)
| Property | Value | Source |
|---|---|---|
| Water Solubility | 57.2 g/L | ALOGPS |
| logP | 1.47 | ALOGPS |
| logP | 1.46 | ChemAxon |
| logS | -0.25 | ALOGPS |
What is the structure of 2 methyl Butan 1?
2-methylbutyric acid is a methylbutyric acid comprising a butyric acid core carrying a 2-methyl substituent. Produced from amino acid leucine during nutrient starvation in bacteria.
What is the functional group of 2 methylbutanoic acid?
alkyl carboxylic acid
2-Methylbutanoic acid, also known as 2-methylbutyric acid is a branched-chain alkyl carboxylic acid with the chemical formula CH3CH2CH(CH3)CO2H, classified as a short-chain fatty acid.
What does isovaleric acid smell like?
Isovaleric acid has a strong pungent cheesy or sweaty smell, but its volatile esters such as ethyl isovalerate have pleasant odors and are widely used in perfumery.
What is the structure of 2 2 Dimethylpropanoic acid?
2,2-dimethylpropanoic acid
| Compound number: | MolPort-001-779-774 |
|---|---|
| IUPAC traditional: | pivalic acid |
| SMILES: | CC(C)(C)C(O)=O |
| InChI key: | IUGYQRQAERSCNH-UHFFFAOYSA-N |
| Molecular formula: | C5H10O2 |
What is the common name for 2 methylbutanoic acid?
2-Methylbutyric acid Methylethylacetic acid
2-Methylbutanoic acid
| Names | |
|---|---|
| Preferred IUPAC name 2-Methylbutanoic acid | |
| Other names 2-Methylbutyric acid Methylethylacetic acid | |
| Identifiers | |
| CAS Number | R/S: 116-53-0 R: 32231-50-8 S: 1730-91-2 |
What is the use of isovaleric acid?
Uses. Isovaleric acid has a strong pungent cheesy or sweaty smell, but its volatile esters such as ethyl isovalerate have pleasant odors and are widely used in perfumery. It is also the primary flavor added to wine when made using Brettanomyces yeasts.
What is the boiling point of 3 methylbutanoic acid?
348.8°F (176°C)
3-Methylbutanoic acid/Boiling point
What is the structure of 2 2 Dimethylbutanoic acid?
2,2-dimethylbutanoic acid
| Compound number: | MolPort-001-787-741 |
|---|---|
| IUPAC traditional: | 2,2-dimethyl butyric acid |
| SMILES: | CCC(C)(C)C(O)=O |
| InChI key: | VUAXHMVRKOTJKP-UHFFFAOYSA-N |
| Molecular formula: | C6H12O2 |
What is the common name of 2 hydroxy propanoic acid?
lactic acid
The common name that is given to 2-hydroxypropanoic acid is lactic acid or milk acid.
What is the formula for 2-methylbutanoic acid?
2-Methylbutanoic acid, also known as 2-methylbutyric acid is a branched-chain alkyl carboxylic acid with the chemical formula CH 3 CH 2 CH (CH 3 )CO 2 H, classified as a short-chain fatty acid. It exists in two enantiomeric forms, ( R )- and ( S )-2-methylbutanoic acid.
What is a methylbutyric acid?
A methylbutyric acid comprising a butyric acid core carrying a 2-methyl substituent. Produced from amino acid leucine during nutrient starvation in bacteria. ChEBI CHEBI:37070, https://www.ebi.ac.uk/chebi/searchId.do?chebiId=CHEBI:37070
How can I obtain the enantiomer of 2-methylbutanoic acid?
Either enantiomer of 2-methylbutanoic acid can now be obtained by asymmetric hydrogenation of tiglic acid using a ruthenium – BINAP catalyst. The compound and its enantiomers react as typical carboxylic acids: they can form amide, ester, anhydride, and chloride derivatives.
What is the Grignard reaction for 2-methylbutanoic acid?
Racemic 2-methylbutanoic acid can readily be prepared by a Grignard reaction using 2-chlorobutane and carbon dioxide. It was the target of the first enantioselective synthesis in 1904 when the German chemist W. Marckwald heated ethyl (methyl)malonic acid with the chiral base brucine and obtained an optically active product mixture.
