CAS 16274-33-2

3,4-Dihydro-2,2-dimethyl-2H-naphtho[1,2-b]pyran

Description:

3,4-Dihydro-2,2-dimethyl-2H-naphtho[1,2-b]pyran, with CAS number 16274-33-2, is an organic compound characterized by its unique bicyclic structure that combines elements of naphthalene and pyran. This compound features a dihydro configuration, indicating the presence of two hydrogen atoms that contribute to its saturation. The two methyl groups attached to the carbon framework enhance its hydrophobic characteristics and influence its reactivity. Typically, compounds of this nature exhibit interesting chemical properties, including potential applications in organic synthesis and materials science. The presence of the pyran ring suggests possible reactivity in electrophilic aromatic substitution reactions, while the naphthalene moiety may contribute to its stability and aromaticity. Additionally, the compound's structural features may impart specific biological activities, making it a subject of interest in medicinal chemistry. Overall, 3,4-Dihydro-2,2-dimethyl-2H-naphtho[1,2-b]pyran represents a fascinating example of complex organic chemistry with potential implications in various fields.

3,4-Dihydro-2,2-Dimethyl-2H-Naphtho[1,2-B]pyran

CAS: 16274-33-2

Formula: C₁₅H₁₆O

Molecular weight: 212.2869

Ref: IN-DA001TDW

3,4-Dihydro-2,2-dimethyl-2H-naphtho[1,2-b]pyran

CAS: 16274-33-2

3,4-Dihydro-2,2-dimethyl-2H-naphtho_1,2-b_pyran is a natural product of Galium, Rubiaceae.

Formula: C₁₅H₁₆O

Purity: 98%

Color and Shape: Solid

Molecular weight: 212.29

Ref: TM-TN2874

3,4-Dihydro-2,2-dimethyl-2H-naphtho[1,2-b]pyran

CAS: 16274-33-2

Formula: C₁₅H₁₆O

Purity: 95%~99%

Color and Shape: Oil

Molecular weight: 212.292

Ref: BP-SBP01717

3,4-Dihydro-2,2-dimethyl-2H-naphtho[1,2-b]pyran

CAS: 16274-33-2

3,4-Dihydro-2,2-dimethyl-2H-naphtho[1,2-b]pyran is an advanced photochromic compound, which is synthesized from naphthalene and pyran structures. This compound, upon exposure to ultraviolet light, undergoes a structural transformation that results in a reversible change in color. The mode of action involves the absorption of UV radiation causing a conformational change in the molecular structure, enabling the compound to switch between two forms with differing optical properties.

Formula: C₁₅H₁₆O

Purity: Min. 95%

Molecular weight: 212.29 g/mol

Ref: 3D-RAA27433