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97510-86-6

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97510-86-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 97510-86-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,7,5,1 and 0 respectively; the second part has 2 digits, 8 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 97510-86:
(7*9)+(6*7)+(5*5)+(4*1)+(3*0)+(2*8)+(1*6)=156
156 % 10 = 6
So 97510-86-6 is a valid CAS Registry Number.

97510-86-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name potassium 2-chloro nicotinate

1.2 Other means of identification

Product number -
Other names potassium 2-chloro-nicotinate

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:97510-86-6 SDS

97510-86-6Upstream product

97510-86-6Relevant articles and documents

Novel strobilurin derivatives containing carboxylate unit as potential antifungal agents

Bao, Longzhu,Cao, Xiufang,Song, Di,Wang, Jingjing,Wang, Shuangshuang,Yue, Xiali

, p. 300 - 311 (2020/04/17)

Background: Due to the extensive use of a single fungicide to control crop diseases, the increase of resistant individuals leads to control failures. The search for molecules with fungicidal activity is still ongoing. Strobilurin is one of the most popularly used fungicides in the agrochemical field. A large number of strobilurin derivatives with both high activity and low toxicity have been developed. Methods: In the present study, a series of novel ortho-substituted benzyl carboxylates were efficiently synthesized by the reaction of (E)-methyl 2-(2-(bromom-ethyl)phenyl)-2-methoxyiminoaceta with various carboxylic acids. Their structures were confirmed and characterized by1H NMR,13C NMR, and ESI-MS analysis. Their fungicidal activities against common phytopathogenic fungi from six major cash crops were screened based on the pesticides guidelines for the laboratory bioactivity tests. Results: The primary fungicidal activity test results indicate that all compounds showed a certain inhibitory effect on the growth of 13 plants pathogenic fungi at a concentration of 100 ppm, and Compd 3 has the most obvious inhibitory effect on all fungi. Further fungicidal activity studies indicate that some of these novel strobilurin derivatives containing carboxylate unit exhibited potential in vitro fungicidal activities at the dosage of 6.25 mg·L-1. Conclusion: A series of the ortho-substituted benzyl carboxylates derivatives containing β-methoxyacrylate moiety were designed and synthesized by modifying the side chain of traditional strobilurin fungicide. Compd 3, Compd 2 and Compd 16 were identified as the most promising candidates for further study.

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