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Phenol, 2-[5-(trifluoromethyl)-1H-benzimidazol-2-yl]- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

104619-92-3

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104619-92-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 104619-92-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,4,6,1 and 9 respectively; the second part has 2 digits, 9 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 104619-92:
(8*1)+(7*0)+(6*4)+(5*6)+(4*1)+(3*9)+(2*9)+(1*2)=113
113 % 10 = 3
So 104619-92-3 is a valid CAS Registry Number.

104619-92-3SDS

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-[(5-trifluoromethyl)-1H-benzimidazol-2-yl]phenol

1.2 Other means of identification

Product number -
Other names 2-(5-Trifluoromethyl-1H-benzoimidazol-2-yl)-phenol

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:104619-92-3 SDS

104619-92-3Relevant academic research and scientific papers

6,7-Dihydrobenzo[f]benzo[4,5]imidazo[1,2-d][1,4]oxazepine derivatives as selective inhibitors of PI3Kα

Yin, Yong,Zhang, Yan-Qing,Jin, Biao,Sha, Shao,Wu, Xun,Sangani, Chetan B.,Wang, She-Feng,Qiao, Fang,Lu, Ai-Min,Lv, Peng-Cheng,Zhu, Hai-Liang

, p. 1231 - 1240 (2015/03/04)

Twenty eight 6,7-dihydrobenzo[f]benzo[4,5]imidazo[1,2-d][1,4]oxazepine derivatives were synthesized and evaluated their biological activities as PI3K inhibitors. Biological evaluation against four human tumor cell lines revealed that most target compounds

Microwave-assisted one-pot synthesis of 2-(substituted phenyl)-1H- benzimidazole derivatives

Navarrete-Vazquez, Gabriel,Moreno-Diaz, Hermenegilda,Estrada-Soto, Samuel,Torres-Piedra, Mariana,Leon-Rivera, Ismael,Tlahuext, Hugo,Munoz-Muniz, Omar,Torres-Gomez, Hector

, p. 2815 - 2825 (2008/02/11)

A series of 2-(substituted phenyl)-1H-benzimidazole derivatives with various 5-and 6-position substituents (-H, -CH3, -CF3) were synthesized via microwave irradiation using a short synthetic route and Na2S2O5 as oxidant. This simple, fast, and efficient p

Substituted 2-(2-Hydroxyphenyl)benzimidazoles as Potential Agents for the Control of Periodontal Diseases

Coburn, Robert A.,Clark, Michael T.,Evans, Richard T.,Genco, Robert J.

, p. 205 - 208 (2007/10/02)

A series of 16 substituted 2-(2-hydroxyphenyl)benzimidazoles was synthesized and evaluated in vitro for antibacterial activity against bacteria associated with periodontal diseases.Several compounds demonstrated a high level of activity, in tube dilution

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