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4-chloro-1-N-propylbenzene-1,2-diamine is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

1040083-67-7

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1040083-67-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1040083-67-7 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,4,0,0,8 and 3 respectively; the second part has 2 digits, 6 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 1040083-67:
(9*1)+(8*0)+(7*4)+(6*0)+(5*0)+(4*8)+(3*3)+(2*6)+(1*7)=97
97 % 10 = 7
So 1040083-67-7 is a valid CAS Registry Number.

1040083-67-7Downstream Products

1040083-67-7Relevant academic research and scientific papers

Hit-to-lead optimization of novel benzimidazole phenylacetamides as broad spectrum trypanosomacides

Avery, Vicky M.,Baell, Jonathan,McNamara, Nicole,Rahmani, Raphael,Sykes, Melissa L.

, p. 685 - 695 (2020/08/24)

Trypanosoma cruzi and Trypanosoma brucei are the parasitic causative agents of Chagas disease and human African trypanosomiasis (HAT), respectively. The drugs currently used to treat these diseases are not efficacious against all stages and/or parasite sub-species, often displaying side effects. Herein, we report the SAR exploration of a novel hit, 2-(4-chlorophenyl)-N-(1-propyl-1H-benzimidazol-2-yl)acetamide previously identified from high throughput screens against T. cruzi, Trypanosoma brucei brucei and Leishmania donovani. An informative set of analogues was synthesized incorporating key modifications of the scaffold resulting in improved potency whilst the majority of compounds retained low cytotoxicity against H9c2 and HEK293 cell lines. The SAR observed against T. cruzi broadly matches that observed against T.b. brucei, suggesting the possibility for a broad-spectrum candidate. This class of compounds therefore warrants further investigation towards development as a treatment for Chagas disease and HAT. This journal is

Design and syntheses of a series of novel serotonin3 antagonists

Hori,Suzuki,Yamamoto,Nakajima,Ozaki,Ohtaka

, p. 1832 - 1841 (2007/10/02)

From a structural comparison study between serotonin and serotonin3 (5- HT3) antagonists using a two-dimensional grid template composed of regular hexagons, we deduced structural modification patterns from agonists to antagonists, an

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