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Benzenecarboximidamide, N-2-benzothiazolyl-, also known as 2-(benzothiazol-2-yl)-1H-benzimidazol-1-amine, is a chemical compound with the molecular formula C14H10N4S. It is a white to off-white crystalline solid that is soluble in organic solvents such as dimethyl sulfoxide (DMSO) and methanol. Benzenecarboximidamide,N-2-benzothiazolyl- is primarily used as an intermediate in the synthesis of various pharmaceuticals and agrochemicals, particularly those containing benzimidazole and benzothiazole moieties. The presence of both benzimidazole and benzothiazole rings in the molecule endows it with unique chemical and biological properties, making it a valuable building block in the development of new drugs and pesticides.

2522-25-0

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2522-25-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 2522-25-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,5,2 and 2 respectively; the second part has 2 digits, 2 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 2522-25:
(6*2)+(5*5)+(4*2)+(3*2)+(2*2)+(1*5)=60
60 % 10 = 0
So 2522-25-0 is a valid CAS Registry Number.

2522-25-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name Diflomotecan

1.2 Other means of identification

Product number -
Other names N-benzothiazol-2-yl-benzamidine

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:2522-25-0 SDS

2522-25-0Relevant academic research and scientific papers

Syntheses of [1,2,4]triazolo[1,5-: A] benzazoles enabled by the transition-metal-free oxidative N-N bond formation

Shang, Erchang,Zhang, Junzhi,Bai, Jinyi,Wang, Zhan,Li, Xiang,Zhu, Bing,Lei, Xiaoguang

supporting information, p. 7028 - 7031 (2016/06/09)

A transition-metal-free oxidative N-N bond formation strategy was developed to generate various structurally interesting [1,2,4]triazolo[1,5-a]benzazoles efficiently. The mechanism of the key oxidative N-N bond formation was investigated by using an intramolecular competition reaction. Notably, the first single crystal structure was also obtained to confirm the structure of 2-aryl[1,2,4]triazolo[1,5-a]benzimidazole.

Efficient Synthesis of Polyfunctionalized Pyrimidine Derivatives

Mahdavi, Mohammad,Kianfard, Hossein,Saeedi, Mina,Ranjbar, Parviz Rashidi,Shafiee, Abbas

, p. 1689 - 1692 (2016/07/06)

A simple and direct procedure was developed for the synthesis of a novel series of polyfunctionalized pyrimidines. They were prepared via reaction of N-(substituted carbamothioyl)benzimidamides (prepared from the reaction of benzimidamide hydrochloride an

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