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N-[(2-hydroxyphenyl)methyl]formamide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

86386-68-7

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86386-68-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 86386-68-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,6,3,8 and 6 respectively; the second part has 2 digits, 6 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 86386-68:
(7*8)+(6*6)+(5*3)+(4*8)+(3*6)+(2*6)+(1*8)=177
177 % 10 = 7
So 86386-68-7 is a valid CAS Registry Number.

86386-68-7Downstream Products

86386-68-7Relevant academic research and scientific papers

METHOD OF CARBON MONOXIDE FIXATION AND METHOD OF AMINE FORMYLATION

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Paragraph 0078; 0081-0085; 0096-0098, (2021/02/19)

The present invention relates to a method for fixing carbon monoxide in a metal-free condition and a method for formating amine using the same.

Metal-free Carbon Monoxide (CO) Capture and Utilization: Formylation of Amines

Noh, Hyeong-Wan,An, Youngjoon,Lee, Seulchan,Jung, Jaehoon,Son, Seung Uk,Jang, Hye-Young

, (2019/04/26)

The capture and utilization of CO by 1,5,7-triazabicyclo[4.4.0]dec-5-ene (TBD) were performed in the absence of transition-metal complexes. The reaction of TBD with CO afforded TBD-CO adducts, which were converted to formylated TBD (TBD-CHO). TBD-CO adducts may include an interaction of CO with positively charged species based on NMR and IR analysis. In the presence of amines, CO was transferred from TBD-CO to amines, producing formylated amines with good yields. The reaction mechanism involving TBD-CO adducts is presented based on theoretical calculations. (Figure presented.).

Synthesis of 3,4-dihydro-2H-1,3-benzoxazine-2-thiones via cyclization of 2-(1-isothiocyanatoalkyl)phenols

Kobayashi, Kazuhiro,Inouchi, Hiroki,Matsumoto, Naoki,Chikazawa, Yuuki

, p. 63 - 74 (2017/03/11)

Convenient sequences for the preparation of 3,4-dihydro-2H-1,3-benzoxazine-2-thiones from 2-hydroxybenzaldehyde and 2-hydroxyphenyl ketones or 2-methylphenols have been developed, which both employ cyclization of 2-(1-isothiocyanatoalkyl)phenols generated

Leuckart-Wallach Route Toward Isocyanides and Some Applications

Neochoritis, Constantinos G.,Zarganes-Tzitzikas, Tryfon,Stotani, Silvia,D?mling, Adrian,Herdtweck, Eberhardt,Khoury, Kareem,D?mling, Alexander

supporting information, p. 493 - 499 (2015/09/22)

Isocyanide-based multicomponent reactions (IMCR) are among the most important chemical reactions to efficiently generate molecular diversity and have found widespread use in industry and academia. Generally, isocyanides are synthesized in 1-2 steps starting from primary amines. Here, we provide experimental detail on an alternative approach toward formamides and, thus, isocyanides via the Leuckart-Wallach reaction in an improved variation. The resulting >50 synthesized and characterized formamides are useful starting materials for IMCR, as well as other chemistries. The advantage of using the Leuckart-Wallach pathway to formamides and isocyanides is the lower price, on average, of the starting materials, as well as their differential and complementary structural diversity, as compared to the primary amine pathway.

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