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"Benzenamine, N-[(5-bromo-2-furanyl)methylene]-" is a chemical compound with the molecular formula C12H8BrNO2. It is an aromatic amine derivative, characterized by the presence of a benzene ring and a furan ring connected through a methylene bridge. The compound features a bromine atom attached to the furan ring, which contributes to its reactivity and potential applications in chemical synthesis. This specific structure may be used in the preparation of various pharmaceuticals, agrochemicals, or other specialty chemicals due to its unique reactivity and functional groups.

3680-91-9

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3680-91-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 3680-91-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,6,8 and 0 respectively; the second part has 2 digits, 9 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 3680-91:
(6*3)+(5*6)+(4*8)+(3*0)+(2*9)+(1*1)=99
99 % 10 = 9
So 3680-91-9 is a valid CAS Registry Number.

3680-91-9Relevant academic research and scientific papers

Sulfated polyborate: A dual catalyst for the reductive amination of aldehydes and ketones by NaBH4

Ganwir, Prerna,Chaturbhuj, Ganesh

supporting information, (2021/05/19)

An efficient, quick, and environment-friendly one-pot reductive amination of aldehydes or ketones was developed. In ethanol at 70 °C, a imination catalyzed by sulfated polyborate and further reduced by sodium borohydride yields various amines. The present method has many significant benefits, including a shorter reaction time, excellent yields, and a hassle-free, straightforward experimental process. The reaction has a wide range of applications due to its flexibility, including secondary amine for reductive amination.

Skeletal Wagner-Meerwein rearrangement of perhydro-3a,6;4,5- diepoxyisoindoles

Zubkov, Fedor I.,Zaytsev, Vladimir P.,Nikitina, Eugeniya V.,Khrustalev, Victor N.,Gozun, Sergey V.,Boltukhina, Ekaterina V.,Varlamov, Alexey V.

scheme or table, p. 9148 - 9163 (2011/12/01)

An investigation of a skeletal Wagner-Meerwein rearrangement of variously substituted or quinoline-annulated 3a,6;4,5-diepoxyisoindol-1-ones is reported. Optimum reaction conditions (Ac2O, BF3·OEt 2, rt) were discovered fo

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