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(E)-4-(2,4,6-trichlorophenyl)but-3-en-2-one is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

1290100-54-7

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1290100-54-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1290100-54-7 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,9,0,1,0 and 0 respectively; the second part has 2 digits, 5 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 1290100-54:
(9*1)+(8*2)+(7*9)+(6*0)+(5*1)+(4*0)+(3*0)+(2*5)+(1*4)=107
107 % 10 = 7
So 1290100-54-7 is a valid CAS Registry Number.

1290100-54-7Downstream Products

1290100-54-7Relevant academic research and scientific papers

Dehydrozingerone Inspired Discovery of Potential Broad-Spectrum Fungicidal Agents as Ergosterol Biosynthesis Inhibitors

Song, Xiangmin,Zhu, Xinyue,Li, Ting,Liang, Cai,Zhang, Meng,Shao, Yu,Tao, Jun,Sun, Ranfeng

, p. 11354 - 11363 (2019/10/16)

A series of dehydrozingerone derivatives were synthesized, and their fungicidal activities and action mechanism against Colletotrichum musae were evaluated. The bioassay result showed that most compounds exhibited excellent fungicidal activity in vitro at 50 μg mL-1. Compounds 13, 16, 18, 19, and 27 exhibited broad-spectrum fungicidal activity; especially, compounds 19 and 27 were found to have more potent fungicidal activity than azoxystrobin. The EC50 values of compounds 19 and 27 against Rhizoctonia solani were 0.943 and 0.161 μg mL-1 respectively. Moreover, compound 27 exhibited significant in vitro bactericidal activity against Xanthomonas oryzae pv. oryzae, with an EC50 value of 11.386 μg mL-1, and its curative effect (49.64%) and protection effect (51.74%) on rice bacterial blight disease was equivalent to that of zhongshengmycin (42.90%, 40.80% respectively). Compound 27 could also effectively control gray mold (87.10%, 200 μg mL-1) and rice sheath blight (100%, 200 μg mL-1 82.89%, 100 μg mL-1) in vivo. Preliminary action mechanism study showed that compound 27 mainly acted on the cell membrane and significantly inhibited ergosterol biosynthesis in Colletotrichum musae.

NOVEL MICROBIOCIDES

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Page/Page column 19, (2012/08/27)

Compounds of formula (I), in which the substituents are as defined in claim 1, are suitable for use as microbiocides.

NOVEL MICROBIOCIDES

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Page/Page column 40, (2011/05/05)

Compounds of formula (I), in which the substituents are as defined in claim 1, are suitable for use as microbiocides.

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