CAS 99-67-2

2-(2-Propenyl)-4-pentenoic acid

Description:

2-(2-Propenyl)-4-pentenoic acid, also known as 2-propenyl-4-pentenoic acid, is an organic compound characterized by its unsaturated carboxylic acid structure. It features a pentenoic acid backbone with a propenyl group at the second carbon position, contributing to its reactivity and potential applications in organic synthesis. This compound is typically a colorless to pale yellow liquid with a distinctive odor. It is soluble in organic solvents and exhibits moderate solubility in water due to the presence of the carboxylic acid functional group. The presence of multiple double bonds in its structure makes it susceptible to polymerization and other addition reactions, which can be exploited in various chemical processes. Additionally, 2-(2-Propenyl)-4-pentenoic acid can serve as a building block in the synthesis of more complex molecules, including polymers and other functionalized compounds. Safety precautions should be observed when handling this substance, as it may cause irritation to the skin and eyes.

Formula: C₈H₁₂O₂

InChI: InChI=1S/C8H12O2/c1-3-5-7(6-4-2)8(9)10/h3-4,7H,1-2,5-6H2,(H,9,10)

InChI key: InChIKey=OKJQSUPURXTNME-UHFFFAOYSA-N

SMILES: C(CC=C)(CC=C)C(O)=O

Synonyms:

• 4-Pentenoic acid, 2-(2-propenyl)-
• 2-(2-Propen-1-yl)-4-pentenoic acid
• 4-Pentenoic acid, 2-(2-propen-1-yl)-
• 2-Allyl-4-pentenoic acid
• 4-Pentenoic acid, 2-allyl-

Valproic Acid Related Compound A

CAS: 99-67-2

Unsaturated acyclic monocarboxylic acids, their anhydrides, halides, peroxides, peroxyacids and their derivatives, nesoi

Formula: C₈H₁₂O₂

Color and Shape: Clear Liquid

Molecular weight: 140.08373

Ref: 45-1708729

Valproic Acid USP Related Compound A

CAS: 99-67-2

Formula: C₈H₁₂O₂

Molecular weight: 140.18

Ref: 4Z-V-0631

Diallylacetic acid

CAS: 99-67-2

Diallylacetic acid

Formula: C₈H₁₂O₂

Purity: 95%

Molecular weight: 140.18

Ref: 54-OR1034043

4-Pentenoic acid, 2-(2-propen-1-yl)-

CAS: 99-67-2

Formula: C₈H₁₂O₂

Purity: 95%

Color and Shape: Liquid

Molecular weight: 140.1797

Ref: IN-DA0065I1

Diallylacetic Acid

CAS: 99-67-2

Formula: C₈H₁₂O₂

Color and Shape: Neat

Molecular weight: 140.18

Ref: 86-MM0751.17

Diallylacetic Acid

Controlled Product

CAS: 99-67-2

Impurity Valproic Acid USP Related Compound A
Applications Diallylacetic Acid (Valproic Acid USP Related Compound A), is a metabolite of Valproic Acid (V094750) as anticonvulsant agents. It can also be used for the synthesis of Velbanamine.
References Liu, H., et al.: Beilstein J. Org. Chem., 9, 983 (2013); Loscher, W., Prog. Neurobiol., 58, 31 (1999); Netzeva, T., et al.: Pharmac. Res., 17, 727 (2000);

Formula: C₈H₁₂O₂

Color and Shape: Neat

Molecular weight: 140.18

Ref: TR-D416010

Valproic Acid USP Related compound A

CAS: 99-67-2

Formula: C₈H₁₂O₂

Molecular weight: 140.18

Ref: ST-EA-CP-V6019

2-Allylpent-4-enoic acid

CAS: 99-67-2

Formula: C₈H₁₂O₂

Molecular weight: 140.18

Ref: BE-RMCV021024

2-Allylpent-4-enoic acid

CAS: 99-67-2

Formula: C₈H₁₂O₂

Purity: 95%

Molecular weight: 140.182

Ref: 10-F363949

Valproic Acid Related Compound A

CAS: 99-67-2

2-Allylpent-4-enoic acid

Formula: C₈H₁₂O₂

Purity: 95%

Molecular weight: 140.18

Ref: IN-DG267657

Valproic acid related compound A

CAS: 99-67-2

Valproic acid related compound A is a polycarboxylic acid that can be polymerized to form polyolefins. Polyolefins are homogeneous catalysts for the production of various ester compounds, and are used in the industrial production of plasticizers, lubricants, and surfactants. Valproic acid related compound A is also a peroxide that can be used as a polymerization initiator in the polymerization of polycarboxylic acids. This chemical is also a functional group with an -OH group on one side and a formyl group on the other.

Formula: C₈H₁₂O₂

Purity: Min. 95%

Color and Shape: Clear Liquid

Molecular weight: 140.18 g/mol

Ref: 3D-AAA09967