CAS 55170-74-6
:5-methylhex-5-enoic acid
Description:
5-Methylhex-5-enoic acid, with the CAS number 55170-74-6, is an unsaturated carboxylic acid characterized by a six-carbon chain with a double bond and a methyl group at the fifth carbon position. This compound features a terminal carboxylic acid functional group, which imparts acidic properties and enhances its reactivity. The presence of the double bond contributes to its unsaturation, making it more reactive in addition reactions compared to saturated fatty acids. 5-Methylhex-5-enoic acid is typically a colorless to pale yellow liquid at room temperature and has a distinctive odor. It is soluble in organic solvents and exhibits moderate solubility in water due to the polar carboxylic acid group. This compound can be used in various chemical syntheses, including the production of polymers and other organic compounds. Its reactivity and structural features make it a valuable intermediate in organic chemistry and industrial applications. Safety precautions should be observed when handling this substance, as it may cause irritation to the skin and eyes.
Formula:C7H12O2
InChI:InChI=1/C7H12O2/c1-6(2)4-3-5-7(8)9/h1,3-5H2,2H3,(H,8,9)
SMILES:C=C(C)CCCC(=O)O
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Found 3 products.
5-Methyl-5-hexenoic acid
CAS:Formula:C7H12O2Purity:97.0%Color and Shape:LiquidMolecular weight:128.1715-Methyl-5-hexenoic acid
CAS:<p>5-Methyl-5-hexenoic acid is a synthetic chemical that can be used as a marker for biochemical pathways. It is synthesized from hydrochloric acid and boron trifluoride etherate, which are heated together at 130°C until all the HCI has been evaporated. 5-Methyl-5-hexenoic acid is then reacted with an amide to produce a fatty acid. Oxazolidinones are often used to synthesize this compound, although it can also be made through dehydrating and anhydrous sodium chloride. The product contains impurities and diastereomers that must be removed before it can be used in the manufacture of pharmaceuticals.</p>Formula:C7H12O2Purity:Min. 95%Molecular weight:128.17 g/mol


