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CAS 4222-20-2: 3,3-Diphenyl-3H-naphtho[2,1-b]pyran
Formula:C25H18O
InChI:InChI=1S/C25H18O/c1-3-10-20(11-4-1)25(21-12-5-2-6-13-21)18-17-23-22-14-8-7-9-19(22)15-16-24(23)26-25/h1-18H
InChI key:InChIKey=UBNNJVRNPJVYBU-UHFFFAOYSA-N
SMILES:C1(OC=2C(C=C1)=C3C(=CC2)C=CC=C3)(C4=CC=CC=C4)C5=CC=CC=C5
Synonyms:- 2,2-Diphenyl-5,6-benzo(2H)chromene
- 3,3-Diphenyl-3H-benzo[f]chromene
- 3,3-Diphenylbenzo[f]chromene
- 3H-Naphtho[2,1-b]pyran, 3,3-diphenyl-
- D 3197
- Photopia AQ Ink Yellow
- Variacrol Yellow L
- 3,3-Diphenyl-3H-naphtho[2,1-b]pyran
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Found 5 products.
3,3-Diphenyl-3H-benzo[f]chromene
CAS:Formula:C25H18OPurity:98%Color and Shape:SolidMolecular weight:334.40983,3-Diphenyl-3H-Benzo[f]Chromene
CAS:3,3-Diphenyl-3H-Benzo[f]ChromenePurity:98%Molecular weight:334.41g/mol3,3-Diphenyl-3H-naphtho[2,1-b]pyran
CAS:Formula:C25H18OPurity:>98.0%(HPLC)Color and Shape:White to Light yellow powder to crystalMolecular weight:334.423,3-Diphenyl-3H-naphtho[2,1-b]pyran
CAS:3,3-Diphenyl-3H-naphtho[2,1-b]pyran is a functional group that is found in many organic compounds. It can be derived from the ring-opening of naphthalene to form biphenyl. The reaction scheme for this process is shown below: The kinetic data for this reaction were obtained by measuring the rate constants and the activation energies. A spectrometer was used to identify the functional groups present in the product. FTIR spectroscopy was used to determine the photochemical properties of 3,3-diphenyl-3H-naphtho[2,1-b]pyran as well as its mass spectrometric data. The mechanism for this reaction is unknown but it may be due to an electron transfer reaction or a hydrogen transfer reaction.END>>Purity:Min. 95%Ref: 3D-FD62474
Discontinued product
![3,3-Diphenyl-3H-benzo[f]chromene](/_next/image/?url=https%3A%2Fstatic.cymitquimica.com%2Fproducts%2FIN%2Fthumb%2FDA003IDS.jpg&w=3840&q=75)
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