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6-hydroxy-9-(4-methoxyphenyl)-1H-phenalen-1-one is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

87618-30-2

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87618-30-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 87618-30-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,7,6,1 and 8 respectively; the second part has 2 digits, 3 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 87618-30:
(7*8)+(6*7)+(5*6)+(4*1)+(3*8)+(2*3)+(1*0)=162
162 % 10 = 2
So 87618-30-2 is a valid CAS Registry Number.

87618-30-2Downstream Products

87618-30-2Relevant 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.

Colouring Matters of Australian Plants. XXIV. Haemofluorone B: New Synthetic Models and a Revised Structure

Chaffee, Alan L.,Cooke, Raymond G.,Dagley, Ian J.,Perlmutter, Patrick,Thomas, Raymond L.

, p. 587 - 598 (2007/10/02)

The occurrence of haemofluorone B in Anigozanthos rufus and Conostylis setosa has been confirmed.The revised structure 5,8,9-trihydroxy-3H-naphthoxanthen-3-one is now proposed for this pigment.Dihydroxyanigorufone has also been found in Conostylis setosa and the structure 9-(3,4-dihydroxyphenyl)-2-hydroxy-1H-phenalen-1-one has been confirmed by synthesis of the trimethyl ether.Some model arylphenalenones and naphthoxanthenones have been prepared from naphthylphenylpropanones and some unusual products have been obtained by photolysis of arylphenalenones and by the reactions of Grignard reagents with phenalenones.

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