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(4-Hydroxyphenyl)(1H-indol-3-yl)methanone, also known as 4-hydroxyphenyl-3-indolylketone, is an organic compound with the molecular formula C15H11NO2. It is a white crystalline solid that is formed by the condensation of 4-hydroxybenzaldehyde and indole-3-carboxaldehyde. (4-HYDROXYPHENYL)(1H-INDOL-3-YL)METHANONE is of interest in the field of organic chemistry and may have potential applications in the synthesis of pharmaceuticals and other chemical products due to its unique structure that combines a hydroxyphenyl group with an indolyl group. The presence of both aromatic and heterocyclic moieties in the molecule suggests it could be a precursor to various biologically active compounds or a building block in the creation of more complex molecules.

98647-12-2

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98647-12-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 98647-12-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,8,6,4 and 7 respectively; the second part has 2 digits, 1 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 98647-12:
(7*9)+(6*8)+(5*6)+(4*4)+(3*7)+(2*1)+(1*2)=182
182 % 10 = 2
So 98647-12-2 is a valid CAS Registry Number.
InChI:InChI=1/C15H11NO2/c17-11-7-5-10(6-8-11)15(18)13-9-16-14-4-2-1-3-12(13)14/h1-9,16-17H

98647-12-2SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name (4-hydroxyphenyl)-(1H-indol-3-yl)methanone

1.2 Other means of identification

Product number -
Other names -

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
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More Details:98647-12-2 SDS

98647-12-2Downstream Products

98647-12-2Relevant academic research and scientific papers

Palladium catalyzed addition of arylboronic acid or indole to nitriles: Synthesis of aryl ketones

Das, Tuluma,Chakraborty, Amarnath,Sarkar, Amitabha

supporting information, p. 7198 - 7202 (2015/01/09)

Aryl ketones can be synthesized conveniently by a palladium catalyzed addition of arylboronic acid to nitriles in aqueous triflic acid. This catalytic system was extended to the addition of unprotected indoles to nitriles under a slightly modified condition to produce 3-acyl indoles in good yields.

COMPOUNDS AND METHODS FOR TREATING PROTEIN FOLDING DISORDERS

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Page/Page column 95, (2008/12/05)

The invention is directed to compounds and methods for treating protein folder disorders. In certain embodiments the invention provides compounds and methods for treating neurodegenerative diseases such as Alzheimer's disease, tauopathy, cerebral amyloid angiopathy, Lewy body disease, dementia, Huntington's disease and prion-based spongiform encelopathy. The invention further provides compounds, methods and pharmaceutical compositions for inhibiting tau protein, Aβ protein or α-synuclein protein aggregation.

Acylindole derivatives and their use in pharmaceutical compositions

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, (2008/06/13)

The present invention is concerned with novel acylindole derivatives of the formula (I) and platelet-aggregation inhibiting agents containing them as an active ingredient. STR1 In the formula (I), either R1 and R2 is hydrogen, an alk

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