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P-aminobenzene-β-hydroxyethyl sulfide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

19284-82-3

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19284-82-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 19284-82-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,9,2,8 and 4 respectively; the second part has 2 digits, 8 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 19284-82:
(7*1)+(6*9)+(5*2)+(4*8)+(3*4)+(2*8)+(1*2)=133
133 % 10 = 3
So 19284-82-3 is a valid CAS Registry Number.

19284-82-3Relevant academic research and scientific papers

Efficient reduction of nitroarenes over nickel-iron mixed oxide catalyst prepared from a nickel-iron hydrotalcite precursor

Shi, Qixun,Lu, Rongwen,Lu, Lianhai,Fu, Xinmei,Zhao, Defeng

, p. 1877 - 1881 (2007)

Nickel-iron mixed oxide prepared from a nickel-iron hydrotalcite precursor was found to be a highly efficient catalyst for the chemoselective reduction of nitroarenes under mild reaction conditions.

Preparation method of p-aminobenzene-beta-hydroxyethylsulfone sulfate

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Paragraph 0082-0083, (2018/01/14)

The invention provides a preparation method of p-aminobenzene-beta-hydroxyethylsulfone sulfate. In the preparation method, parachloronitrobenzene is used as a raw material, and is subjected to reaction steps of reduction, condensation, acylation, catalytic oxidation, esterification and the like, and therefore, the p-aminobenzene-beta-hydroxyethylsulfone sulfate which is high in yield and high in quality can be prepared.

Visible-light-promoted radical C-H trifluoromethylation of free anilines

Xie, Jin,Yuan, Xiangai,Abdukader, Ablimit,Zhu, Chengjian,Ma, Jing

supporting information, p. 1768 - 1771 (2014/04/17)

The trifluoromethyl-substituted anilines are biologically active compounds and useful building blocks. In this communication, we have developed the first visible-light-induced radical trifluoromethylation of free anilines with the commercially available and easily handled Togni reagent at room temperature. The resulting products were successfully transformed into a variety of valuable fluorine-containing molecules and heterocyclic compounds. This protocol provides an economical and powerful route to trifluoromethylated free anilines.

SYNTHESIS OF C-TERMINAL PEPTIDE FRAGMENTS OF THE HEAVY CHAIN OF HEMAGGLUTININ OF INFLUENZA VIRUS OF SUBTYPES H1 AND H3

Kalashnikov, V. V.,Samukov, V. V.

, p. 624 - 629 (2007/10/02)

It is proposed to use the chromogenic 2-ethyl group, which can be eliminated by organic bases in aprotic solvents, for the protection of a C-terminal carboxy group in the synthesis of peptides.The synthesis of a number of 10-1

GRAPHITE CATAlYZED REDUCTION OF AROMATIC AND ALIPHATIC NITRO COMPOUNDS WITH HYDRAZINE HYDRATE

Han, Byung Hee,Shin, Dae Hyun,Cho, Sung Yun

, p. 6233 - 6234 (2007/10/02)

Aromatic and aliphatic nitro compounds were readily reduced to amino compounds in excellant yields with graphite and hydrazine hydrate.

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