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1-(p-metossibenzil)-2-cloroindol-3-carbossialdeide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

77655-47-1

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77655-47-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 77655-47-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,7,6,5 and 5 respectively; the second part has 2 digits, 4 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 77655-47:
(7*7)+(6*7)+(5*6)+(4*5)+(3*5)+(2*4)+(1*7)=171
171 % 10 = 1
So 77655-47-1 is a valid CAS Registry Number.

77655-47-1Relevant academic research and scientific papers

Synthesis and Antimicrobial Activities of Novel Quinazolinone Acylhydrazone Derivatives Containing the Indole Moiety

Li, Xiao-Qin,Gan, Yi-Yuan,Meng, Jiao,Li, Wen,Chen, Jie,Qi, Ya-Yun,Tian, Kun,Ouyang, Gui-Ping,Wang, Zhen-Chao

, p. 1382 - 1390 (2018/04/25)

A series of novel quinazolinone acylhydrazone derivatives containing the indole moiety were designed, synthesized, and evaluated for their inhibition activities against some important phytopathogens in vitro. Antibacterial experiments indicated that some compounds exhibited remarkable inhibition activities against tested bacteria. Especially, the EC50 values of 7a (EC50?=?55.13?μg/mL against Xoo, EC50?=?56.92?μg/mL against Rs) demonstrated the best antibacterial activities against Xoo and Rs than the other compounds, and the control agents Bismerthiazol (EC50?=?89.80?μg/mL against Xoo) and Thiodiazole copper (EC50?=?189.52?μg/mL against Rs), moreover, compound 7o (EC50?=?50.80?μg/mL) displayed the excellent activity against Xac than the control Bismerthiazol (EC50?=?56.92?μg/mL).

SINTESI ED ATTIVITA ANTIBATTERICA IN VITRO DI N-METILNITRONI E NITROVINILI DERIVATI DA ALCUNE 2-CLOROINDOL-3-CARBOSSIALDEIDI N-SOSTITUITE

Gatti, R.,Cavrini, V.,Roveri, P.,Bianucci, F.,Legnani, P.

, p. 102 - 108 (2007/10/02)

N-methylnitrones and nitrovinyl derivatives from 1-substituted-2-chloroindole-3-carboxaldehydes were synthesized and evaluated for their in vitro antibacterial activity.Some nitrovinyl derivatives displayed good in vitro activity against Gram-positive bacteria; the compound (II e), 1-(o-chlorobenzyl)-2-chloro-3-(2-nitroethenyl)indole, was more active than nitrofurantoin against Staphylococcus aureus and Streptococcus pyogenes.Some structure-activity relationships are discussed.

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