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2-(2-methyl-1H-indol-3-yl)cyclohexa-2,5-diene-1,4-dione is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

80641-49-2

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80641-49-2 Usage

Structure

Derivative of indole and cyclohexane

Usage

Research and synthesis in organic chemistry

Pharmaceutical potential

Interest in medicinal chemistry due to indole moiety

Biological activity

Potential for further exploration in drug development or treatment

Versatility

Potential uses in various scientific and medical applications

Check Digit Verification of cas no

The CAS Registry Mumber 80641-49-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,0,6,4 and 1 respectively; the second part has 2 digits, 4 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 80641-49:
(7*8)+(6*0)+(5*6)+(4*4)+(3*1)+(2*4)+(1*9)=122
122 % 10 = 2
So 80641-49-2 is a valid CAS Registry Number.
InChI:InChI=1/C15H11NO2/c1-9-15(11-4-2-3-5-13(11)16-9)12-8-10(17)6-7-14(12)18/h2-8,16H,1H3

80641-49-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-(2-methyl-1H-indol-3-yl)cyclohexa-2,5-diene-1,4-dione

1.2 Other means of identification

Product number -
Other names 2-(2'-methylindol-3-yl)-1,4-benzoquinone

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:80641-49-2 SDS

80641-49-2Downstream Products

80641-49-2Relevant academic research and scientific papers

Light induced activity switch in interfacial hydrogen-bond catalysis with photo sensitive metal oxides

Niu, Fang,Zhai, Jin,Jiang, Lei,Song, Wei-Guo

supporting information; experimental part, p. 4738 - 4740 (2010/01/16)

UV light switches on the catalytic activities of several metal oxides in hydrogen bond catalyzed reactions because of the changes in the concentration of the surface hydroxyl groups. The Royal Society of Chemistry 2009.

Promotion of organic reactions by interfacial hydrogen bonds on hydroxyl group rich nano-solids

Niu, Fang,Liu, Chang-Chang,Cui, Zhi-Min,Zhai, Jin,Jiang, Lei,Song, Wei-Guo

supporting information; body text, p. 2803 - 2805 (2009/02/05)

Surface hydroxyl group rich nano-structured solids dramatically increase the rate of several organic reactions; such effect is attributed to the formation of interfacial hydrogen bonds between the surface hydroxyl groups and the reactants; this catalytic

Novel synthesis of 3-indolylquinones catalyzed by molecular iodine under ultrasonic irradiation

Liu, Bing,Ji, Shun-Jun,Su, Xiao-Ming,Wang, Shun-Yi

, p. 1279 - 1290 (2008/09/18)

The conjugate addition reactions of indoles with quinones were catalyzed efficiently by molecular iodine under ultrasonic irradiation to afford 3-indolylquinones in good to excellent yields, which provided a novel, mild, convenient approach for the prepar

"On water"-promoted direct coupling of indoles with 1,4-benzoquinones without catalyst

Zhang, Hai-Bo,Liu, Li,Chen, Yong-Jun,Wang, Dong,Li, Chao-Jun

, p. 869 - 873 (2007/10/03)

A highly efficient direct coupling of indole compounds with 1,4-benzoquinones was developed "on water" in the absence of any catalyst, organic co-solvent, or additives. The "on-water" conditions provided the best yields of the corresponding products and the only system to produce bis(coupling) products. Wiley-VCH Verlag GmbH & Co. KGaA, 2006.

ACID-CATALYZED REACTIONS OF INDOLES WITH 1,4-QUINONES

Corradini, Maria Grazia,Costantini, Claudio,Prota, Giuseppe,Schultz, Thomas M.

, p. 153 - 156 (2007/10/02)

Under anaerobic conditions, indoles with unsubstituted 3-positions react with 1,4-benzoquinone and 1,4-naphthoquinone in acidic solution to give intensely coloured 2-(3-indolyl)quinones in good yields.In the case of 3-methylindole, the reaction with 1,4-n

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