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C-Pyridin-4-yl-methylamine; hydrochloride is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

18205-56-6

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18205-56-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 18205-56-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,8,2,0 and 5 respectively; the second part has 2 digits, 5 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 18205-56:
(7*1)+(6*8)+(5*2)+(4*0)+(3*5)+(2*5)+(1*6)=96
96 % 10 = 6
So 18205-56-6 is a valid CAS Registry Number.

18205-56-6Downstream Products

18205-56-6Relevant academic research and scientific papers

Fabrication of ω-Transaminase@Metal-Organic Framework Biocomposites for Efficiently Synthesizing Benzylamines and Pyridylmethylamines

Yu, Jinhai,Zong, Weilu,Ding, Yingying,Liu, Junzhong,Chen, Lina,Zhang, Hongjuan,Jiao, Qingcai

, p. 380 - 390 (2021/11/05)

In this study, ten ω-transaminases (ω-TAs) have been investigated to efficiently catalyze the synthesis of twenty-four functionalized benzylamines and pyridylmethylamines. We optimized the reactions, screened suitable amino donors and compared ω-transaminases activities for all aromatic aldehyde substrates. Under the optimized conditions, eighteen aromatic amines have been obtained with 60.4%–96.6% conversions and isolated only via simple extraction and recrystallization with 18.5%–81% yields on a preparative scale. Furthermore, we first immobilized the Bm-STA onto the MOFs via the physical adsorption to overcome the limitation of free enzyme and improve their industrial applications. The obtained Bm-STA/UiO-66-NH2 composites exhibited not only high enzymes loading (80.4 mg g?1) and enzyme activity recovery (95.8%), but also the better reusability, storage stability, pH stability and the tolerance to acetone and DMF.

A Facile Preparation of 4-(1-acetyl-4(1H)-pyridylidene)-2-oxazolin-5-ones

Hirota, Kazuhiro,Shimamura, Michiya,Ikeda, Mikiko,Ohmori, Shinji

, p. 1551 - 1552 (2007/10/02)

4-(1-Acetyl-4(1H)-pyridylidene)-2-oxazolin-5-ones were prepared by the reaction of acylglycines with pyridine and acetic anhydride under oxygen.Acidic and alkaline hydrolysis of 2-oxazolin-5-ones provided oxazole derivatives, pyridine derivatives and carboxylic acids.

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