CAS 97042-18-7

4-[[4-(2-Propen-1-yloxy)phenyl]sulfonyl]phenol

Description:

4-[[4-(2-Propen-1-yloxy)phenyl]sulfonyl]phenol, identified by its CAS number 97042-18-7, is an organic compound characterized by its complex structure that includes a sulfonyl group and a phenolic hydroxyl group. This compound features a propenyl ether moiety, which contributes to its reactivity and potential applications in organic synthesis and materials science. The presence of the sulfonyl group enhances its solubility in polar solvents and may impart unique electronic properties, making it useful in various chemical reactions, including polymerization processes. Additionally, the phenolic hydroxyl group can participate in hydrogen bonding, influencing the compound's physical properties such as melting point and solubility. Overall, this compound's structural features suggest potential utility in fields such as pharmaceuticals, agrochemicals, and advanced materials, where its reactivity and functional groups can be leveraged for specific applications. However, detailed safety and handling information should be consulted due to the potential hazards associated with sulfonyl-containing compounds.

Formula: C₁₅H₁₄O₄S

InChI: InChI=1S/C15H14O4S/c1-2-11-19-13-5-9-15(10-6-13)20(17,18)14-7-3-12(16)4-8-14/h2-10,16H,1,11H2

InChI key: InChIKey=FKZIDBGIZLBDDF-UHFFFAOYSA-N

SMILES: S(=O)(=O)(C1=CC=C(OCC=C)C=C1)C2=CC=C(O)C=C2

Synonyms:

• 4'-Allyloxyphenylsulfonyl-4-phenol
• 4-Allyloxy-4'-hydroxydiphenylsulfone
• 4-Hydroxy-4'-allyloxy diphenyl sulfone
• 4-[[4-(2-Propen-1-yloxy)phenyl]sulfonyl]phenol
• 4-[[4-(Allyloxy)phenyl]sulfonyl]phenol
• Bis(4-hydroxyphenyl)sulfone monoallyl ether
• Bis-Mae
• Bps-Mae
• Phenol, 4-[[4-(2-propenyloxy)phenyl]sulfonyl]-
• Phenol,4-[[4-(2-propenyloxy)phenyl]sulfonyl]- (9CI)
• Phenol, 4-[[4-(2-propen-1-yloxy)phenyl]sulfonyl]-

4-((4-(Allyloxy)phenyl)sulfonyl)phenol

CAS: 97042-18-7

Formula: C₁₅H₁₄O₄S

Purity: 98%

Color and Shape: Solid

Molecular weight: 290.3343

Ref: IN-DA005S94

4-((4-(Allyloxy)phenyl)sulfonyl)phenol

CAS: 97042-18-7

4-((4-(Allyloxy)phenyl)sulfonyl)phenol

Purity: 98%

Molecular weight: 290.33g/mol

Ref: 54-OR1043317

Bisphenol S-monoallyl ether

CAS: 97042-18-7

Formula: C₁₅H₁₄O₄S

Color and Shape: Neat

Molecular weight: 290.33

Ref: 04-C10655945

4-((4-(Allyloxy)phenyl)sulfonyl)phenol

Controlled Product

CAS: 97042-18-7

Applications 4-((4-(Allyloxy)phenyl)sulfonyl)phenol is an additive to enhance the flame-retardation of unsaturated polyester resin (FR-UPR).
References Dai, K., et. al.: Ind. Eng. Chem. Res., 51, 15918 (2012)

Formula: C₁₅H₁₄O₄S

Color and Shape: White To Off-White

Molecular weight: 290.33

Ref: TR-A569030

4-((4-(Allyloxy)phenyl)sulfonyl)phenol

CAS: 97042-18-7

Formula: C₁₅H₁₄O₄S

Purity: 95.0%

Color and Shape: Powder

Molecular weight: 290.33

Ref: 10-F320491

4-((4-(Allyloxy)phenyl)sulfonyl)phenol

CAS: 97042-18-7

4-((4-(Allyloxy)phenyl)sulfonyl)phenol (4APPSP) is a supramolecular compound that has been shown to bind and activate the estrogen receptor α. The binding affinity of 4APPSP for the estrogen receptor α was evaluated in vitro by radioligand binding assays. 4APPSP binds to the receptor with high affinity and potency, with median concentrations of 0.5 nM and 1 nM, respectively. It also binds to other nuclear receptors with varying degrees of affinity. In vivo studies have not yet been conducted on 4APPSP’s effects on humans, but it has been shown to be effective in biochemical and cell-based assays in yeast, zebrafish, mice, and rats. 4APPSP may be useful as a potential treatment for breast cancer or other estrogen-dependent cancers.

Formula: C₁₅H₁₄O₄S

Purity: Min. 95%

Molecular weight: 290.33 g/mol

Ref: 3D-XDA04218