CAS 13997-73-4

2-Allyl-4-chlorophenol

Description:

2-Allyl-4-chlorophenol, with the CAS number 13997-73-4, is an organic compound characterized by its phenolic structure, which includes a chlorine substituent and an allyl group. This compound typically appears as a colorless to pale yellow liquid and possesses a distinctive aromatic odor. It is soluble in organic solvents but has limited solubility in water due to its hydrophobic characteristics. The presence of the chlorine atom enhances its reactivity, making it useful in various chemical syntheses and applications. 2-Allyl-4-chlorophenol exhibits antimicrobial properties, which can be advantageous in formulations for preservatives or disinfectants. Additionally, it may participate in electrophilic aromatic substitution reactions due to the electron-withdrawing nature of the chlorine atom, influencing its reactivity and interaction with other chemical species. Safety precautions should be observed when handling this compound, as it may pose health risks if inhaled or ingested, and appropriate protective equipment should be used to mitigate exposure.

Formula: C₉H₉ClO

InChI: InChI=1S/C9H9ClO/c1-2-3-7-6-8(10)4-5-9(7)11/h2,4-6,11H,1,3H2

InChI key: InChIKey=NQZKLVHWFYHXGH-UHFFFAOYSA-N

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

Synonyms:

• 4-Chloro-2-(2-propen-1-yl)phenol
• 4-Chloro-2-(Prop-2-En-1-Yl)Phenol
• 4-Chloro-2-allylphenol
• Ai3-39001
• Nsc 1539
• Phenol, 2-allyl-4-chloro-
• Phenol, 2-allyl-4-chloro- (8CI)
• Phenol, 4-chloro-2-(2-propen-1-yl)-
• Phenol, 4-chloro-2-(2-propenyl)-
• Phenol, 4-chloro-2-(2-propenyl)- (9CI)
• 2-Allyl-4-chlorophenol

4-Chloro-2-(prop-2-en-1-yl)phenol

CAS: 13997-73-4

Formula: C₉H₉ClO

Color and Shape: Solid

Molecular weight: 168.6202

Ref: IN-DA001BWB

2-Allyl-4-chlorophenol

CAS: 13997-73-4

2-Allyl-4-chlorophenol is a synthetic antioxidant that scavenges reactive oxygen species. It is also considered to be an environmental pollutant and has been shown to inhibit the production of 4-allyl-2-methoxyphenol, which is a metabolite of the natural antioxidant α-tocopherol. 2-Allyl-4-chlorophenol reacts with water molecules and transfers electrons to hydrogen peroxide, which may lead to the formation of hypochlorous acid. 2-Allyl-4-chlorophenol has inhibitory properties against oxidative stress, particularly in submandibular gland cells. This inhibition may be due to its redox potential, which is higher than that of other antioxidants such as α-tocopherol or eugenol.

Formula: C₉H₉ClO

Purity: Min. 95%

Color and Shape: Powder

Molecular weight: 168.62 g/mol

Ref: 3D-FA150954

2-allyl-4-chloro-phenol

CAS: 13997-73-4

Formula: C₉H₉ClO

Purity: 95.0%

Color and Shape: No data available.

Molecular weight: 168.62

Ref: 10-F515373

4-Chloro-2-(prop-2-en-1-yl)phenol

Controlled Product

CAS: 13997-73-4

Formula: C₉H₉ClO

Color and Shape: Neat

Ref: TR-B421158