CAS 1076-99-9

4-(prop-2-en-1-yl)benzoic acid

Description:

4-(Prop-2-en-1-yl)benzoic acid, also known as p-allylbenzoic acid, is an organic compound characterized by a benzoic acid structure with an allyl group (prop-2-en-1-yl) attached to the para position of the benzene ring. This compound typically appears as a colorless to pale yellow liquid or solid, depending on its form and purity. It is soluble in organic solvents such as ethanol and ether but has limited solubility in water due to its hydrophobic aromatic ring. The presence of the carboxylic acid functional group imparts acidic properties, allowing it to participate in various chemical reactions, including esterification and amidation. Its structure makes it a useful intermediate in organic synthesis, particularly in the production of polymers and pharmaceuticals. Additionally, 4-(prop-2-en-1-yl)benzoic acid can undergo polymerization reactions, making it valuable in materials science. Safety data should be consulted for handling, as it may pose health risks if ingested or inhaled.

Formula: C₁₀H₁₀O₂

InChI: InChI=1/C10H10O2/c1-2-3-8-4-6-9(7-5-8)10(11)12/h2,4-7H,1,3H2,(H,11,12)

InChI key: InChIKey=YBCFIVNTXHMQGZ-UHFFFAOYSA-N

SMILES: C(O)(=O)C1=CC=C(CC=C)C=C1

Synonyms:

• 4-(2-Propen-1-yl)benzoic acid
• 4-Allyl-benzoic acid
• 4-Allylbenzoic acid
• Benzoic acid, 4-(2-propen-1-yl)-
• Benzoic acid, 4-(2-propenyl)-
• Benzoic acid, p-allyl-
• 4-(2-PROPENYL)BENZOIC ACID
• 4-prop-2-enylbenzoic acid

4-ALLYL-BENZOIC ACID

CAS: 1076-99-9

Formula: C₁₀H₁₀O₂

Purity: 95%

Color and Shape: Solid

Molecular weight: 162.1852

Ref: IN-DA008UTE

4-(2-Propenyl)benzoic acid

CAS: 1076-99-9

4-(2-Propenyl)benzoic acid

Purity: 95%

Molecular weight: 162.19g/mol

Ref: 54-OR1045599

4-(2-Propenyl)benzoic acid

CAS: 1076-99-9

Formula: C₁₀H₁₀O₂

Purity: 95%

Color and Shape: Liquid, No data available.

Molecular weight: 162.188

Ref: 10-F200774

4-(Prop-2-en-1-yl)benzoic acid

CAS: 1076-99-9

Glycinamide ribonucleotide (GAR) is a glycinamide that is used as an inhibitor of formyltransferase. It forms a reversible covalent bond with the active site cysteine residue of the enzyme, thereby inhibiting its activity. GAR has been shown to inhibit both eukaryotic and prokaryotic formyltransferases, and also inhibits the related enzyme ribonucleotide reductase. This compound may have potential for use in treating cancer due to its ability to inhibit tumor growth by interfering with DNA synthesis.

Formula: C₁₀H₁₀O₂

Purity: Min. 95%

Molecular weight: 162.18 g/mol

Ref: 3D-BAA07699