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2-(1H-Indol-3-yl)-4-(6-bromo-1H-indol-3-yl)-1H-imidazole is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

134029-45-1

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134029-45-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 134029-45-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,4,0,2 and 9 respectively; the second part has 2 digits, 4 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 134029-45:
(8*1)+(7*3)+(6*4)+(5*0)+(4*2)+(3*9)+(2*4)+(1*5)=101
101 % 10 = 1
So 134029-45-1 is a valid CAS Registry Number.

134029-45-1SDS

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 6-bromo-3-[2-(1H-indol-3-yl)-1H-imidazol-5-yl]-1H-indole

1.2 Other means of identification

Product number -
Other names Nortopsentin C

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:134029-45-1 SDS

134029-45-1Downstream Products

134029-45-1Relevant academic research and scientific papers

Marine-Natural-Product Development: First Discovery of Nortopsentin Alkaloids as Novel Antiviral, Anti-phytopathogenic-Fungus, and Insecticidal Agents

Ji, Xiaofei,Guo, Jincheng,Liu, Yuxiu,Lu, Aidang,Wang, Ziwen,Li, Yongqiang,Yang, Shaoxiang,Wang, Qingmin

, p. 4062 - 4072 (2018/05/03)

Nortopsentin alkaloids were found to have potent antiviral, anti-phytopathogenic-fungus, and insecticidal activities for the first time. Antiviral-activity tests revealed that these compounds were very sensitive to substituents, so a series of nortopsentin derivatives were designed, synthesized, and systematically evaluated for their antiviral activities against TMV, their fungicidal activities, and their insecticidal activities on the basis of a structural-diversity-derivation strategy. Compounds 2e (in vivo inactivation-, curative-, and protective-activity inhibitory rates of 50, 59, and 56%, respectively, at 500 μg/mL) and 2k (in vivo inactivation-, curative-, and protective-activity inhibitory rates of 60, 58, and 52%, respectively, at 500 μg/mL), with excellent antiviral activities and good physicochemical properties, emerged as new lead compounds for novel-antiviral-agent development. Further fungicidal-activity tests revealed that these alkaloids displayed broad-spectrum fungicidal activities. Compounds 2f, 2h, and 2j emerged as new lead compounds for antifungal-activity research. Additionally, all the compounds displayed good insecticidal activities against five kinds of insects, including Mythimna separate, Helicoverpa armigera, Ostrinia nubilalis, Plutella xylostella, and Culex pipiens pallens.

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