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tert-butyl (4-methyl-1-phenylpent-1-yn-3-yl)carbamate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

950522-80-2

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950522-80-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 950522-80-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,5,0,5,2 and 2 respectively; the second part has 2 digits, 8 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 950522-80:
(8*9)+(7*5)+(6*0)+(5*5)+(4*2)+(3*2)+(2*8)+(1*0)=162
162 % 10 = 2
So 950522-80-2 is a valid CAS Registry Number.

950522-80-2Downstream Products

950522-80-2Relevant academic research and scientific papers

Graphitic Carbon Nitride Polymer as a Recyclable Photoredox Catalyst for Decarboxylative Alkynylation of Carboxylic Acids

Guo, Jiaqi,Wang, Yating,Li, Yuhang,Lu, Kailin,Liu, Shihui,Wang, Wei,Zhang, Yongqiang

supporting information, p. 3898 - 3904 (2020/08/07)

Visible-light-induced heterogeneous photocatalysis for decarboxylative alkynylation has been performed. The using of cheap, metal-free and recyclable graphitic carbon nitride (g-C3N4) as the photoredox catalyst in the process enables

9,10-Dicyanoanthracene Catalyzed Decarboxylative Alkynylation of Carboxylic Acids under Visible-Light Irradiation

Yang, Chen,Yang, Jin-Dong,Li, Yi-He,Li, Xin,Cheng, Jin-Pei

, p. 12357 - 12363 (2016/12/23)

A metal-free, visible-light-induced photocatalytic procedure for decarboxylative alkynylation of carboxylic acids was reported. With 9,10-dicyanoanthracene as the photoredox catalyst, the reaction covered a broad scope of α-amino acids, α-oxo acids, and α-keto acids with blue LED irradiation at room temperature under an atmosphere of argon, delivering alkynyl products in moderate to excellent yields. Natural sun light also promoted this alkynylation strategy. This work represents the first example of an organophotocatalytic method for decarboxylative alkynylation of carboxylic acids.

Synthesis of N-Boc-Propargylic and Allylic Amines by Reaction of Organomagnesium Reagents with N-Boc-Aminals and Their Oxidation to N-Boc-Ketimines

Kano, Taichi,Kobayashi, Ryohei,Maruoka, Keiji

supporting information, p. 276 - 279 (2016/02/03)

Previously inaccessible N-Boc-protected propargylic and allylic amines were synthesized by the reaction between N-Boc-aminals and organomagnesium reagents through the in situ generated N-Boc-imine intermediates. The obtained N-Boc-propargylic amines could be readily converted into unprecedented N-Boc-ketimines by oxidation with manganese dioxide.

A practical gold-catalyzed route to 4-substituted oxazolidin-2-ones from N-Boc propargylamines

Lee, Eun-Sun,Yeom, Hyun-Suk,Hwang, Ji-Hyun,Shin, Seunghoon

, p. 3503 - 3507 (2008/02/12)

Au1-catalyzed cyclization of N-Boc propargylamines into 4-alkylidene oxazolidin-2-ones is described. This modular approach provides access to a variety of nonproteogenic 4-substituted oxazolidinones that are important in asymmetric synthesis an

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