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2-azido-3-(4-nitrophenyl)-1-phenylprop-2-en-1-one is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

26087-02-5

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26087-02-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 26087-02-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,6,0,8 and 7 respectively; the second part has 2 digits, 0 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 26087-02:
(7*2)+(6*6)+(5*0)+(4*8)+(3*7)+(2*0)+(1*2)=105
105 % 10 = 5
So 26087-02-5 is a valid CAS Registry Number.

26087-02-5Relevant academic research and scientific papers

Access to Imidazole Derivatives by Silver(I) Carbonate Mediated Coupling of Vinyl Azides with Secondary Amines

Adiyala, Praveen Reddy,Borra, Satheesh,Kamal, Ahmed,Maurya, Ram Awatar

, p. 1269 - 1273 (2016)

An efficient protocol for the synthesis of structurally diverse imidazoles by Ag2CO3-mediated coupling of vinyl azides with secondary amines was developed, and 22 different examples were synthesized in good to high yields. This operationally simple synthetic strategy allows the formation of three new C-N bonds by cascade reactions that involve sp3 C-H functionalization.

Continuous-flow photo-induced decarboxylative annulative access to fused imidazole derivatives: Via a microreactor containing immobilized ruthenium

Adiyala, Praveen Reddy,Jang, Seungwook,Vishwakarma, Niraj K.,Hwang, Yoon-Ho,Kim, Dong-Pyo

supporting information, p. 1565 - 1571 (2020/03/26)

Visible-light-driven continuous-flow decarboxylative annulation was achieved and used along with a microreactor containing immobilized ruthenium catalyst to construct valuable fused imidazole derivatives with high yields under an open atmosphere. Notably, this chemistry included the use of l-proline and α-azidochalcone as precursors of an α-amino radical and 2H-azirine via photo-induced decarboxylation and denitrogenation, respectively, to give the annulated imidazole derivatives as a result of the formation of two new C-N bonds. Moreover the novel, environmentally benign and efficient continuous-flow protocol was further improved by carrying out the reaction in a polydimethylsiloxane (PDMS) microreactor with immobilized Ru3+ under fluorescent or white LED light, enabling excellent yields (70-94%) at a reaction time (2 min) significantly shorter than that (16 h) of the batch protocol.

Access to Imidazo[1,2-a]pyridines via Annulation of α-Keto Vinyl Azides and 2-Aminopyridines

Adiyala, Praveen Reddy,Mani, Geeta Sai,Nanubolu, Jagadeesh Babu,Shekar, Kunta Chandra,Maurya, Ram Awatar

supporting information, p. 4308 - 4311 (2015/09/15)

A novel strategy for the synthesis of imidazo[1,2-a]pyridines via efficient catalyst/metal-free annulations of α-keto vinyl azides and 2-aminopyridines is described. Several imidazo[1,2-a]pyridines were synthesized from readily available vinyl azides and

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