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3-{2-[(6-oxocyclohexa-2,4-dien-1-ylidene)methyl]hydrazino}-2H-indol-2-one is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

70565-00-3

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70565-00-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 70565-00-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,0,5,6 and 5 respectively; the second part has 2 digits, 0 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 70565-00:
(7*7)+(6*0)+(5*5)+(4*6)+(3*5)+(2*0)+(1*0)=113
113 % 10 = 3
So 70565-00-3 is a valid CAS Registry Number.

70565-00-3SDS

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-[2-[(E)-(6-oxocyclohexa-2,4-dien-1-ylidene)methyl]hydrazinyl]indol-2-one

1.2 Other means of identification

Product number -
Other names 3-salicylidenehydrazono-2-indolinone

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:70565-00-3 SDS

70565-00-3Downstream Products

70565-00-3Relevant academic research and scientific papers

Pharmacological characteristics of some 3-salicylidenehydrazono-2- indolinone coordination compounds

Konstantinovi?, Sandra S.,Caki?, Vanja S.

, p. 771 - 781 (2010)

1 3-Salicylidenehydrazono-2-indolinone (SHI) complexes with Co(II), Ni(II), Cu(II), Zn(II), and Pd(II) were synthesized. All compounds were evaluated for their antimicrobial activity against seven pathogenic bacteria and four fungi. The compounds also hav

Application of SBA-Pr-SO3H in the green synthesis of isatinhydrazone derivatives: Characterization, UV-Vis investigation and computational studies

Gholamzadeh, Parisa,Mohammadi Ziarani, Ghodsi,Badiei, Alireza

, p. 2935 - 2939 (2016/10/06)

An efficient and green synthesis is developed for the preparation of the arylidene isatinhydrazone derivatives 4a-m using a heterogeneous mesoporous acid catalyst of SBA-Pr-SO3H with a pore size of 6 nm under solvent free conditions. The hydrazones 4a-m were then analyzed by UV-Vis spectroscopy and the results were used for the calculation of the HOMO-LUMO band gap. In addition, the quantum chemical calculations were performed to provide an illustrative explanation for the obtained band gap; it is found that probably these molecules have a high tendency to donate electrons to the appropriate small-molecule acceptors with low energy and empty molecular orbital.

Synthesis leishmanicidal activities of bis-Schiff bases of isatins

Khan, Momin,Khan, Khalid Mohammed,Rahim, Fazal,Samreen,Perveen, Shahnaz,Karim, Aneela,Imtiazuddin,Choudhary, Muhammad Iqbal

, p. 520 - 526 (2015/08/04)

Twenty seven (27) derivatives of bis-Schiff bases of isatins 1-27 were studied for their leishmanicidal potential. Out of twenty seven (27) analogs, five exhibited varying degree of leishmanicidal activity with IC50 values 44.86 ± 0.66, 65.27 ±

Superoxide respiratory burst inhibitory activity of bis-schiff bases of Isatins

Khan, Khalid Mohammed,Khan, Momin,Ali, Muhammad,Qadir, Muhammad Irfan,Perveen, Shahnaz,Karim, Aneela,Choudhary, Muhammad Iqbal

, p. 987 - 993 (2013/07/26)

Bis-Schiff bases 1-27 were synthesized and evaluated for their anti-inflammatory activity and possible cytotoxicity. Compounds 1-27 showed a varying degree of respiratory burst inhibitory activity with IC50 values between 242.97 - 652.12 μM. Co

Synthesis of bis-Schiff bases of isatins and their antiglycation activity

Khan, Khalid Mohammed,Khan, Momin,Ali, Muhammad,Taha, Muhammad,Rasheed, Saima,Perveen, Shahnaz,Choudhary, M. Iqbal

experimental part, p. 7795 - 7801 (2010/03/30)

Bis-Schiff bases 1-27 have been synthesized and their in vitro antiglycation potential has been evaluated. Compounds 21 (IC50 = 243.95 ± 4.59 μM), 20 (IC50 = 257.61 ± 5.63 μM), and 7 (IC50 = 291.14 ± 2.53 μM) showed an exc

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