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N-(1,1'-Biphenyl)-2-yl-N-hydroxyacetamide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

30272-56-1

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30272-56-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 30272-56-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,0,2,7 and 2 respectively; the second part has 2 digits, 5 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 30272-56:
(7*3)+(6*0)+(5*2)+(4*7)+(3*2)+(2*5)+(1*6)=81
81 % 10 = 1
So 30272-56-1 is a valid CAS Registry Number.
InChI:InChI=1/C14H13NO2/c1-11(16)15(17)14-10-6-5-9-13(14)12-7-3-2-4-8-12/h2-10,17H,1H3

30272-56-1SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name N-hydroxy-N-(2-phenylphenyl)acetamide

1.2 Other means of identification

Product number -
Other names N-Biphenyl-2-ylacetohydroxamsaeure

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:30272-56-1 SDS

30272-56-1Downstream Products

30272-56-1Relevant academic research and scientific papers

Catalyst-free generation of acyl radicals induced by visible light in water to construct C-N bonds

Ran, Maogang,He, Jiaxin,Yan, Boyu,Liu, Wenbo,Li, Yi,Fu, Yunfen,Li, Chao-Jun,Yao, Qiuli

supporting information, p. 1970 - 1975 (2021/03/16)

We describe herein a catalyst-free and redox-neutral photochemical strategy for the direct generation of acyl radicals from α-diketones, and its selective conversion of nitrosoarenes to hydroxyamides or amides with AcOH or NaCl as an additive. The reaction was carried out under mild conditions in water with purple LEDs as the light source. A broad scope of substrates was demonstrated. Mechanistic experiments indicate that α-diketones cleave to give acyl radicals, with hydroxyamides being further reduced to amides.

Synthesis method of N-acylhydroxylamine

-

Paragraph 0053-0055, (2020/09/30)

The invention relates to a synthesis method of N-acylhydroxylamine, which comprises the following steps: starting from o-diketone and a nitroso compound, and adding an acid thereby efficiently obtaining the structure of N-acylhydroxylamine under the irradiation of visible light or ultraviolet light, wherein a part of the obtained product is an important biomedical chemical intermediate. Accordingto the method, the o-diketone and the nitroso compound which are cheap and easy to obtain are used as raw materials, only visible light or ultraviolet light irradiation is needed, cheap acid is addedin the reaction process, a catalyst or a metal compound is not needed, and only water can be used as a solvent in mass production. The whole production process is environmentally friendly, economical,efficient and low in cost, and has very remarkable advantages compared with the conventional production process.

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