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681160-67-8

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681160-67-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 681160-67-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 6,8,1,1,6 and 0 respectively; the second part has 2 digits, 6 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 681160-67:
(8*6)+(7*8)+(6*1)+(5*1)+(4*6)+(3*0)+(2*6)+(1*7)=158
158 % 10 = 8
So 681160-67-8 is a valid CAS Registry Number.

681160-67-8Relevant articles and documents

Synthesis, Crystal Structure, Herbicidal Activity, and SAR Study of Novel N-(Arylmethoxy)-2-chloronicotinamides Derived from Nicotinic Acid

Yu, Chen-Sheng,Wang, Qiao,Bajsa-Hirschel, Joanna,Cantrell, Charles L.,Duke, Stephen O.,Liu, Xing-Hai

, p. 6423 - 6430 (2021/06/28)

Nicotinic acid, also known as niacin, is a natural product, which is widely found in plants and animals. To discover novel natural-product-based herbicides, a series of N-(arylmethoxy)-2-chloronicotinamides were designed and synthesized. Some of the new N-(arylmethoxy)-2-chloronicotinamides exhibited excellent herbicidal activity against Agrostis stolonifera (bentgrass) at 100 μM. Compound 5f (2-chloro-N-((3,4-dichlorobenzyl)oxy)nicotinamide) possessed excellent herbicidal activity against Lemna paucicostata (duckweed), with an IC50 value of 7.8 μM, whereas the commercial herbicides clomazone and propanil had values of 125 and 2 μM, respectively. The structure-activity relationships reported in this paper could be used for the development of new herbicides against monocotyledonous weeds.

Ultrasound accelerated synthesis of: O-alkylated hydroximides under solvent- A nd metal-free conditions

Jiang, Hongmei,Tang, Xiaoyue,Liu, Sihan,Wang, Lian,Shen, Haicheng,Yang, Jiankui,Wang, Huixian,Gui, Qing-Wen

, p. 10223 - 10227 (2019/12/26)

A novel, sustainable, environmentally friendly, high substrate scope, efficient, solvent-free and metal catalyst-free method for the cross-dehydrogenative coupling (CDC) reaction between N-hydroxyphthalimide (NHPI) and benzyl/ether compounds is described. This coupling reaction proceeds through ultrasound acceleration. Compared to conventional heating conditions, the use of ultrasound techniques not only improves the reaction efficiency and enhances the reaction rate but also minimizes the side reactions.

Method for preparing PINO (phthimide-n-oxyl) derivatives through directly coupling NHPI (n-hydroxyphthalimide)and benzyl-containing compounds under non-metal catalysis

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Paragraph 0040; 0041; 0045 - 0047; 0060 - 0062, (2017/04/22)

The invention discloses a method for preparing PINO (phthimide-n-oxyl) derivatives through directly coupling NHPI (n-hydroxyphthalimide) and benzyl-containing compounds under non-metal catalysis. According to the method, under the nitrogen protection, the

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