CAS 1200-89-1

Cyclopentadiene-Benzoquinone Adduct (1:1)

Description:

Cyclopentadiene-Benzoquinone Adduct (1:1), with the CAS number 1200-89-1, is a chemical compound formed through the Diels-Alder reaction between cyclopentadiene and benzoquinone. This adduct typically exhibits a stable structure characterized by a fused bicyclic system, which contributes to its unique reactivity and properties. The compound is known for its potential applications in organic synthesis and materials science due to its ability to undergo further chemical transformations. It is generally a solid at room temperature and may display a range of colors depending on its purity and specific formulation. The adduct is also notable for its electron-rich nature, which can influence its reactivity in subsequent reactions, making it a valuable intermediate in the synthesis of more complex organic molecules. Safety precautions should be observed when handling this compound, as it may pose health risks if inhaled or ingested, and appropriate personal protective equipment should be used.

Formula: C₁₁H₁₀O₂

InChI: InChI=1/C11H10O2/c12-8-3-4-9(13)11-7-2-1-6(5-7)10(8)11/h1-4,6-7,10-11H,5H2

InChI key: InChIKey=FQLRTGXTYFCECH-UHFFFAOYSA-N

SMILES: C1=CC2CC1C1C(=O)C=CC(=O)C21

Synonyms:

• 1,4,4A,8A-Tetrahydro-1,4-Methanonaphthalene-5,8-Dione
• 1,4-Methanonaphthalene-5,8-dione, 1,4,4a,8a-tetrahydro-
• Cyclopentadienebenzoquinone
• NSC 25329
• Tricyclo[6.2.1.0^2,7]undeca-4,9-diene-3,6-dione
• endo-Tricyclo[6.2.1.0(2,7)]undeca-4,9-diene-3,6-dione

1,4,4a,8a-Tetrahydro-1,4-methanonaphthalene-5,8-dione

CAS: 1200-89-1

1,4,4a,8a-Tetrahydro-1,4-methanonaphthalene-5,8-dione

Purity: 98%

Molecular weight: 174.2g/mol

Ref: 54-OR1036206

1,4,4a,8a-Tetrahydro-endo-1,4-methanonaphthalene-5,8-dione

CAS: 1200-89-1

Purity: 98%

Molecular weight: 174.1990051

Ref: 10-F875610

1,4,4a,8a-Tetrahydro-1,4-methano-naphthalene-5,8-dione

CAS: 1200-89-1

1,4,4a,8a-Tetrahydro-1,4-methano-naphthalene-5,8-dione is a cyclopentadiene derivative that is used as an inhibitor of the enzyme quinolinium. It has been shown to inhibit the activity of quinolinium at low concentrations with no detectable effect on other enzymes. The compound was crystallized and its X-ray diffraction pattern showed it to be dihedral (two noncoplanar planes) and stereoselective (the left side of the molecule is active). The compound was also found to have low yields in synthesis and inhibits ethyl cinnamate without affecting pyridinium.

Formula: C₁₁H₁₀O₂

Purity: Min. 95%

Molecular weight: 174.2 g/mol

Ref: 3D-FT137769

1,4,4a,8a-Tetrahydro-endo-1,4-methanonaphthalene-5,8-dione

Controlled Product

CAS: 1200-89-1

Formula: C₁₁H₁₀O₂

Color and Shape: Neat

Molecular weight: 174.2

Ref: TR-T294485