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1H-Indol-5-ol, 2-(4-hydroxyphenyl)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

62613-59-6

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62613-59-6 Usage

Chemical Family

Indole

Structure

A derivative of indole with a hydroxyl group attached at the 4th carbon position of the phenyl ring.

Usage

Synthesis of pharmaceuticals and agrochemicals, research for potential biological activities.

Biological Activities

Exhibits antioxidant, anti-inflammatory, and anti-cancer properties.

Potential Applications

Drug development, medical and agricultural fields.

Check Digit Verification of cas no

The CAS Registry Mumber 62613-59-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,2,6,1 and 3 respectively; the second part has 2 digits, 5 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 62613-59:
(7*6)+(6*2)+(5*6)+(4*1)+(3*3)+(2*5)+(1*9)=116
116 % 10 = 6
So 62613-59-6 is a valid CAS Registry Number.

62613-59-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-(4-hydroxyphenyl)-1H-indol-5-ol

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 -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:62613-59-6 SDS

62613-59-6Downstream Products

62613-59-6Relevant academic research and scientific papers

Programmable genotoxic agents and uses therefor

-

, (2008/06/13)

The compositions and methods disclosed herein provide heterobifunctional programmable genotoxic compounds that can be designed to kill selected cells present in a heterogenous cell population. The present compounds comprise a first agent that inflicts damage on cellular DNA, and a second agent that attracts a macromolecular cell component such as a protein, which in turn shields genomic lesions from repair. Unrepaired lesions therefore persist in the cellular genome and contribute to the death of selected cells. In contrast, lesions formed in nonselected cells, which lack the cell component, are unshielded and thus are repaired. As a result, compounds described herein are less toxic to nonselected cells. Compounds of this invention can be designed to cause the selective killing of transformed cells, viral-infected cells and the like.

2-Phenylindoles. Relationship between Structure, Estrogen Receptor Affinity, and Mammary Tumor Inhibiting Activity in the Rat

Angerer, Erwin von,Prekajac, Jelica,Strohmeier, Josef

, p. 1439 - 1447 (2007/10/02)

A number of 2-phenylindole derivatives with one hydroxy group in the meta or para position of the phenyl ring and a second one in position 5, 6, or 7 of the indole nucleus were synthesized.In addition, different alkyl groups were introduced into positions

2-Phenyl-indole derivatives

-

, (2008/06/13)

The present invention relates to new stabilizers of polymers and co-polymers of vinyl chloride corresponding to the general formula: STR1 wherein R1, R2, R3, R4, R5 and R6, which are the sa

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