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2-bromo-6-mercaptobenzonitrile is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

1374518-01-0

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1374518-01-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1374518-01-0 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,7,4,5,1 and 8 respectively; the second part has 2 digits, 0 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 1374518-01:
(9*1)+(8*3)+(7*7)+(6*4)+(5*5)+(4*1)+(3*8)+(2*0)+(1*1)=160
160 % 10 = 0
So 1374518-01-0 is a valid CAS Registry Number.

1374518-01-0Upstream product

1374518-01-0Downstream Products

1374518-01-0Relevant academic research and scientific papers

Chemical synthesis, crystal structure, versatile evaluation of their biological activities and molecular simulations of novel pyrithiobac derivatives

Wu, Ren-Jun,Zhou, Kai-Xuan,Yang, Haijin,Song, Guo-Qing,Li, Yong-Hong,Fu, Jia-Xin,Zhang, Xiao,Yu, Shu-Jing,Wang, Li-Zhong,Xiong, Li-Xia,Niu, Cong-Wei,Song, Fu-Hang,Yang, Haitao,Wang, Jian-Guo

, p. 472 - 484 (2019)

Since pyrithiobac (PTB) is a successful commercial herbicide with very low toxicity against mammals, it is worth exploring its derivatives for an extensive study. Herein, a total of 35 novel compounds were chemically synthesized and single crystal of 6–6

About the reaction of aryl fluorides with sodium sulfide: Investigation into the selectivity of substitution of fluorobenzonitriles to yield mercaptobenzonitriles via SNAr displacement of fluorine

Taldone, Tony,Patel, Pallav D.,Patel, Hardik J.,Chiosis, Gabriela

supporting information; experimental part, p. 2548 - 2551 (2012/06/15)

In this report we describe a simple synthesis of mercaptobenzonitriles from the reaction of fluorobenzonitriles with Na2S in DMF at room temperature and following direct treatment with Zn/HCl. Significantly, 2- and 4-fluorobenzonitriles substituted with chlorine or bromine, but not iodine, undergo selective substitution of fluorine at room temperature to yield synthetically useful halo-substituted mercaptobenzonitriles.

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