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Phenol, 2-[bis(2-methyl-1H-indol-3-yl)methyl]- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

110200-68-5

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110200-68-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 110200-68-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,0,2,0 and 0 respectively; the second part has 2 digits, 6 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 110200-68:
(8*1)+(7*1)+(6*0)+(5*2)+(4*0)+(3*0)+(2*6)+(1*8)=45
45 % 10 = 5
So 110200-68-5 is a valid CAS Registry Number.

110200-68-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-[bis(2-methyl-1H-indol-3-yl)methyl]phenol

1.2 Other means of identification

Product number -
Other names Phenol,2-[bis(2-methyl-1H-indol-3-yl)methyl]

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:110200-68-5 SDS

110200-68-5Downstream Products

110200-68-5Relevant academic research and scientific papers

Silica Supported Sodium Hydrogen Sulfate and Amberlyst-15: Two Efficient Heterogeneous Catalysts for Facile Synthesis of Bis- and Tris(1H-indol-3-yl) methanes from Indoles and Carbonyl Compounds

Ramesh, Chimmani,Banerjee, Joydeep,Pal, Rammohan,Das, Biswanath

, p. 557 - 559 (2003)

Bis- and tris(1H-indol-3-yl)methanes are synthesized in high yields by an electrophilic substitution reaction of indoles with carbonyl compounds under mild reaction conditions using two efficient heterogeneous catalysts, silica supported sodium hydrogen s

One-pot access to indolylchromeno[2,3-b]indoles via iodine-mediated Friedel-Crafts alkylation/oxidative coupling reaction of indoles and salicylaldehydes

Rong, Guang-Qing,Zhao, Jian-Qiang,Zhang, Xiao-Mei,Xu, Xiao-Ying,Yuan, Wei-Cheng,Zhou, Ming-Qiang

, p. 2383 - 2390 (2018)

An I2-mediated Friedel-Crafts alkylation/oxidative coupling reaction of indoles and salicylaldehydes was developed. With the developed protocol, a series of indolylchromeno[2,3-b]indoles were obtained in good yields (up to 88%) under mild reaction conditions. Two possible reaction mechanisms were tentatively brought forward to account for the formation of the products in light of some control experiments.

The first urea-based ionic liquid-stabilized magnetic nanoparticles: An efficient catalyst for the synthesis of bis(indolyl)methanes and pyrano[2,3-d]pyrimidinone derivatives

Zolfigol, Mohammad Ali,Ayazi-Nasrabadi, Roya,Baghery, Saeed

, p. 273 - 281 (2016/05/02)

Urea-based ionic liquid stabilized on silica-coated Fe3O4 magnetic nanoparticles, {Fe3O4atSiO2@(CH2)3-Urea-SO3H/HCl}, as an unexceptionable and smooth releasing urea f

Glycerol as a promoting medium for electrophilic activation of aldehydes: Catalyst-free synthesis of di(indolyl)methanes, xanthene-1,8(2H)-diones and 1-oxo-hexahydroxanthenes

He, Fei,Li, Peng,Gu, Yanlong,Li, Guangxing

experimental part, p. 1767 - 1773 (2011/02/27)

Glycerol was used, for the first time, as a green and effective promoting medium for electrophilic activation of aldehydes, and with which, a catalyst-free system for some reactions that conventionally carried out using acid catalysts, such as synthesis o

A convenient, rapid and eco-friendly synthesis of bis-indolylmethanes under microwave irradiation

Das, Biswanath,Pal, Rammohan,Banerjee, Joydeep,Ramesh, Chimmani,Mahender, Gurram,Venkateswarlu, Katta

, p. 327 - 330 (2007/10/03)

Silica chloride has been applied as a catalyst for the first time for rapid synthesis of bis-indolylmethanes in excellent yields by electrophilic substitution reaction of indoles with carbonyl compounds under microwave irradiation. The process is environm

Electrophilic Substitution of Indoles: Part IX - Reaction of Indoles with Iminium Systems

Banerji, J.,Saha, M.,Chakrabarti, R.,Das, A. K.,Pandit, U. K.,et al.

, p. 1204 - 1208 (2007/10/02)

The electrophilic substitution of indoles with iminium systems has led to the synthesis of new and interesting heterocyclic compounds, the structures of which have been settled from detailed 1H and 13C NMR studies.

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