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49744-74-3

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49744-74-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 49744-74-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 4,9,7,4 and 4 respectively; the second part has 2 digits, 7 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 49744-74:
(7*4)+(6*9)+(5*7)+(4*4)+(3*4)+(2*7)+(1*4)=163
163 % 10 = 3
So 49744-74-3 is a valid CAS Registry Number.

49744-74-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-hydroxy-2-methyl-1-(4-methylphenyl)pyridin-4-one

1.2 Other means of identification

Product number -
Other names 3-hydroxy-2-methyl-1-p-tolyl-4-pyridone

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:49744-74-3 SDS

49744-74-3Relevant articles and documents

Discovery of N-Aryl-pyridine-4-ones as Novel Potential Agrochemical Fungicides and Bactericides

Yu, Xiuqiang,Zhu, Xinyue,Zhou, Yang,Li, Qinglin,Hu, Zhan,Li, Ting,Tao, Jun,Dou, Menglan,Zhang, Meng,Shao, Yu,Sun, Ranfeng

, p. 13904 - 13913 (2019/12/24)

A series of N-aryl-pyridine-4-one derivatives were designed and synthesized using maltol and antidesmone as lead compounds, and then their fungicidal/bactericidal activities and possible mechanism of action against Colletotrichum musae were explored. Most of these compounds exhibited significant fungicidal activity in vitro. Especially, compound 23 has more than 90% inhibitory activity against nine plant pathogenic fungi at 50 μg mL-1, which is superior to azoxystrobin. Moreover, an in vivo bioassay also demonstrated that compound 23 exhibited high-efficiency broad-spectrum antifungal activity and can effectively control postharvest diseases of mango. In addition, it was found that compounds 22 and 23 can also effectively control rice bacterial leaf blight in pot experiments, which was even more effective than zhongshengmycin. Preliminary mechanism studies revealed that compound 23 may cause cell membrane and mitochondria destruction. These findings indicate that compound 23 can be used to develop potential agrochemical fungicides and bactericides.

Synthesis and Characterization of Some 1-Aryl-3-hydroxy-4(1H)-pyridinones. Solubilities and Their Solvation in Methanol-Water Mixtures.

Burgess, John,Castro, Baltazar de,Oliveira, Celeste,Rangel, Maria

, p. 1338 - 1351 (2007/10/03)

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