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40757-61-7

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40757-61-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 40757-61-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 4,0,7,5 and 7 respectively; the second part has 2 digits, 6 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 40757-61:
(7*4)+(6*0)+(5*7)+(4*5)+(3*7)+(2*6)+(1*1)=117
117 % 10 = 7
So 40757-61-7 is a valid CAS Registry Number.

40757-61-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 11, 2017

Revision Date: Aug 11, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-acetyl-5-methyl-1,2,3-thiadiazole

1.2 Other means of identification

Product number -
Other names 1-(Methyl-[1,2,3]thiadiazol-4-yl)-aethanon

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:40757-61-7 SDS

40757-61-7Upstream product

40757-61-7Relevant articles and documents

Synthesis of 1,2,3-thiadiazole and thiazole-based strobilurins as potent fungicide candidates

Chen, Lai,Zhu, Yu-Jie,Fan, Zhi-Jin,Guo, Xiao-Feng,Zhang, Zhi-Ming,Xu, Jing-Hua,Song, Ying-Qi,Yurievich, Morzherin Y.,Belskaya, Nataliya P.,Bakulev, Vasiliy A.

, p. 745 - 751 (2017/02/10)

Strobilurin fungicides play a crucial role in protecting plants against different pathogens and securing food supplies. A series of 1,2,3-thiadiazole and thiazole-based strobilurins were rationally designed, synthesized, characterized, and tested against various fungi. Introduction of 1,2,3-thiadiazole greatly improved the fungicidal activity of the target molecules. Compounds 8a, 8c, 8d, and 10i exhibited a relatively broad spectrum of fungicidal activity. Compound 8a showed excellent activities against Gibberella zeae, Sclerotinia sclerotiorum, and Rhizoctonia cerealis with median effective concentrations (EC50) of 2.68, 0.44, and 0.01 μg/mL, respectively; it was much more active than positive controls enestroburin, kresoxim-methyl, and azoxystrobin with EC50 between 0.06 and 15.12 μg/mL. Comparable or better fungicidal efficacy of compound 8a compared with azoxystrobin and trifloxystrobin against Sphaerotheca fuliginea and Pseudoperonspera cubensis was validated in cucumber fields at the same application dosages. Therefore, compound 8a is a promising fungicidal candidate worthy of further development.

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