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Acetamide, N-(4-nitrophenoxy)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

90370-48-2

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90370-48-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 90370-48-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,0,3,7 and 0 respectively; the second part has 2 digits, 4 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 90370-48:
(7*9)+(6*0)+(5*3)+(4*7)+(3*0)+(2*4)+(1*8)=122
122 % 10 = 2
So 90370-48-2 is a valid CAS Registry Number.

90370-48-2Downstream Products

90370-48-2Relevant academic research and scientific papers

Cobalt(III)-Catalyzed Intermolecular Carboamination of Propiolates and Bicyclic Alkenes via Non-Annulative Redox-Neutral Coupling

Zhu, Yuelu,Chen, Feng,Zhao, Xinyang,Yan, Dingyuan,Yong, Wanxiong,Zhao, Jing

supporting information, p. 5884 - 5888 (2019/08/20)

A cobalt(III)-catalyzed, redox-neutral, intermolecular carboamination of propiolates and bicyclic alkenes was developed. This non-annulative coupling strategy features atom economy, high regioselectivity, good yields, and functional groups tolerance. Such a carboamination reaction was applied to modified phenols from the corresponding phenols under mild conditions.

Rhodium(III)-Catalyzed Cascade Redox-Neutral C–H Functionalization and Aromatization: Synthesis of Unsymmetrical ortho-Biphenols

Hu, Zhiyong,Liu, Guixia

supporting information, p. 1643 - 1648 (2017/05/22)

An efficient rhodium(III)-catalyzed coupling reaction of N-aryloxyacetamides with 6-diazo-2-cyclohexenones through a cascade redox-neutral C–H functionalization and aromatization has been developed. This novel and scalable transformation provides a straightforward way to construct unsymmetrical ortho-biphenols with broad substrate scope under mild and redox-neutral conditions. The synthetic utility of this approach is demonstrated in the late-stage functionalization of bioactive compounds and the synthesis of an optically active ortho-biphenol. (Figure presented.).

Direct Conversion of Haloarenes to Phenols under Mild, Transition-Metal-Free Conditions

Fier, Patrick S.,Maloney, Kevin M.

supporting information, p. 2244 - 2247 (2016/06/01)

A high-yielding and practical method for the synthesis of phenols from electron-deficient haloarenes and heteroarenes has been developed. The products are formed from acetohydroxamic acid as the hydroxide source via a novel SNAr reaction/Lossen rearrangement sequence. Notably, these reactions employ inexpensive and air-stable reagents, require no special handling, occur under mildly basic conditions, and form products in high yields in the presence of electrophilic and protic functionality. The utility of this methodology is demonstrated by the high-yielding hydroxylation of two base-sensitive complex substrates.

Rhodium(III)-catalyzed C-H olefination for the Synthesis of ortho-alkenyl phenols using an oxidizing directing group

Shen, Yangyang,Liu, Guixia,Zhou, Zhi,Lu, Xiyan

, p. 3366 - 3369 (2013/07/26)

By using an oxidizing directing group, a mild, efficient Rh(III) catalyzed C-H olefination reaction between N-phenoxyacetamides and alkenes was developed. This reaction provided a straightforward way for the synthesis of ortho-alkenyl phenols, and the directing group is traceless in the product.

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