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aniline dithiocarbamate(1-) is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

22296-13-5

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22296-13-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 22296-13-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,2,2,9 and 6 respectively; the second part has 2 digits, 1 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 22296-13:
(7*2)+(6*2)+(5*2)+(4*9)+(3*6)+(2*1)+(1*3)=95
95 % 10 = 5
So 22296-13-5 is a valid CAS Registry Number.

22296-13-5Relevant academic research and scientific papers

Synthesis and nematicidal activity of piperazinedione derivatives based on the natural product Barettin

Sun, Haiyang,Li, Hui,Wang, Jiayi,Song, Gonghua

, p. 977 - 980 (2018)

Nematodes are serious constraints of crop production worldwide. However, the traditional nematicides suffer from the side-effects, including environmental and human toxicity. Herein, more than 70 novel piperazinedione derivatives based on the natural product Barettin were synthesized and evaluated against the root-knot nematode Meloidogyne incognita (M. incognita). While most of synthesized compounds exhibited certain nematicidal activity at high concentration, the best one showed a nematicidal activity of 75% at 2.4 μmol/L.

Iron-promoted one-pot approach: Synthesis of isothiocyanates

Pendem, Venkata Bhavanarushi,Nannapaneni, Madhavi

, p. 485 - 490 (2020/02/18)

We have established a facile and versatile synthesis for the construction of isothiocyanates from their respective amines in the presence of an eco-friendly, inexpensive, easily available Iron catalyst under mild conditions. This reaction provides the target products through the formation of thiocarbamate salt as an intermediate. Both aromatic amines and aliphatic amines provided the respective target products in moderate to high yield under optimized reaction conditions. However, electron withdrawing substituents were difficult to give target product at room temperature, whereas, they obtained final products in good yield at moderate temperature. In addition, mechanistic studies were revealed that the synthetic route involved iron based subsequent reactions of addition and removal of sulfur.

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