Welcome to LookChem.com Sign In|Join Free
  • or
1H-naphtho[2,1,8-mna]xanthen-1-one is a complex organic compound with the molecular formula C23H12O2. It belongs to the class of xanthene derivatives, which are characterized by a fused-ring structure consisting of a benzene ring, a pyran ring, and a pyrrole ring. This particular compound features a naphthalene moiety attached to the xanthene core, with the carbonyl group (C=O) at the 1-position. It is known for its potential applications in the field of organic chemistry, particularly in the synthesis of dyes and pigments, due to its extended conjugated system that can absorb light across the visible spectrum. The compound's structure and properties make it a subject of interest for researchers studying the optical and electronic properties of organic materials.

66946-98-3

Post Buying Request

66946-98-3 Suppliers

Recommended suppliers

  • Product
  • FOB Price
  • Min.Order
  • Supply Ability
  • Supplier
  • Contact Supplier

66946-98-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 66946-98-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,6,9,4 and 6 respectively; the second part has 2 digits, 9 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 66946-98:
(7*6)+(6*6)+(5*9)+(4*4)+(3*6)+(2*9)+(1*8)=183
183 % 10 = 3
So 66946-98-3 is a valid CAS Registry Number.

66946-98-3Downstream Products

66946-98-3Relevant academic research and scientific papers

New Routes to Phenalenones from 2,7-Dihydroxynaphthalene. X-Ray Crystal Structure of 4-(α-Hydroxybenzyl)-2-phenyl-6H-phenaleno-pyran-6-one

Carey, John L.,Thomson, Ronald H.,Cox, Philip J.

, p. 1267 - 1274 (2007/10/02)

9-Aryl-6-hydroxy-1H-phenalen-1-ones and 2-aryl-4-aroyl-6H-phenalenopyran-6-ones can be obtained by the reaction of 2,7-dihydroxyphenalene-1-carbaldehyde with acetophenones and by condensation of aroylacetaldehydes with 2,7-dihydroxynaphthalene under acid conditions.Aroylacetaldehydes may be involved in the former reaction also, arising by transfer of the formyl group from the naphthaldehyde to the acetophenone. 2,7-Dihydroxynaphthalene-1-carbaldehyde reacts with 2-hydroxyacetophenone to form 1H-naphthoxanthen-1-one.Interaction of naphthalene-2,7-dioxybismagnesium dibromide with cinnamaldehydes affords 4-benzyl-2-phenyl-6H-phenalenopyran-6-ones.

Post a RFQ

Enter 15 to 2000 letters.Word count: 0 letters

Attach files(File Format: Jpeg, Jpg, Gif, Png, PDF, PPT, Zip, Rar,Word or Excel Maximum File Size: 3MB)

1 Customer Service

What can I do for you?
Get Best Price

Get Best Price for 66946-98-3