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1-(2-Nitro-benzyl)-3,5,7-triaza-1-azonia-tricyclo[3.3.1.13,7]decane; bromide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

57856-66-3

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57856-66-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 57856-66-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,7,8,5 and 6 respectively; the second part has 2 digits, 6 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 57856-66:
(7*5)+(6*7)+(5*8)+(4*5)+(3*6)+(2*6)+(1*6)=173
173 % 10 = 3
So 57856-66-3 is a valid CAS Registry Number.

57856-66-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-(2-nitrobenzyl)-1,3,5,7-tetraazaadamantan-1-ium bromide

1.2 Other means of identification

Product number -
Other names -

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:57856-66-3 SDS

57856-66-3Relevant academic research and scientific papers

Development of a novel class of pyrrolo-[1,2,5]benzothiadiazepine derivatives as potential anti-schistosomal agents

Chen, Jinglei,Sun, Weizhen,Yang, Jingjing,Sun, Huan,Wang, Zhixia,Dong, Lanlan,Qiao, Chunhua,Xia, Chao-Ming

, p. 3785 - 3787 (2013)

Analogues of pyrrolo-[1,2,5]benzothiadiazepine were prepared and evaluated against Schistosoma japonica. The biological data revealed that most benzothiazepine derivatives show anti-schistosomal activity to some extent, while α-chloronation of the title compound and another bioisosteric derivative pyrrolo-[1,2,5]benzodiazepine displayed the most distinct worm killing activity. This study proved that benzodiazepine may serve as a novel structural skeleton for the development of anti-schistosomal agents.

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