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1-ethyl-2-(4-hydroxyphenyl)-3-methyl-1H-indol-5-ol is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

86111-11-7

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86111-11-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 86111-11-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,6,1,1 and 1 respectively; the second part has 2 digits, 1 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 86111-11:
(7*8)+(6*6)+(5*1)+(4*1)+(3*1)+(2*1)+(1*1)=107
107 % 10 = 7
So 86111-11-7 is a valid CAS Registry Number.

86111-11-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-ethyl-5-hydroxy-2-(4-hydroxyphenyl)-3-methyl-1H-indol

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:86111-11-7 SDS

86111-11-7Downstream Products

86111-11-7Relevant academic research and scientific papers

Modular counter-Fischer?indole synthesis through radical-enolate coupling

Chung, Hyunho,Kim, Jeongyun,Gonzalez-Montiel, Gisela A.,Cheong, Paul Ha-Yeon,Lee, Hong Geun

supporting information, p. 1096 - 1102 (2021/01/26)

A single-electron transfer mediated modular indole formation reaction from a 2-iodoaniline derivative and a ketone has been developed. This transition-metal-free reaction shows a broad substrate scope and unconventional regioselectivity trends. Moreover, important functional groups for further transformation are tolerated under the reaction conditions. Density functional theory studies reveal that the reaction proceeds by metal coordination, which converts a disfavored 5-endo-trig cyclization to an accessible 7-endo-trig process.

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

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