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108262-98-2

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108262-98-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 108262-98-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,8,2,6 and 2 respectively; the second part has 2 digits, 9 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 108262-98:
(8*1)+(7*0)+(6*8)+(5*2)+(4*6)+(3*2)+(2*9)+(1*8)=122
122 % 10 = 2
So 108262-98-2 is a valid CAS Registry Number.

108262-98-2SDS

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 3-[(Z)-4-Bromo-phenylimino]-1-diethylaminomethyl-1,3-dihydro-indol-2-one

1.2 Other means of identification

Product number -
Other names -

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:108262-98-2 SDS

108262-98-2Downstream Products

108262-98-2Relevant articles and documents

Microwave-assisted synthesis and evaluation of indole derivatives as potential anthelmintic agents

Panda, Jnyanaranjan,Kumar, Anjan,Sahoo, Biswa Mohan,Banik, Bimal Krishna

, p. 1283 - 1288 (2020/06/27)

An efficient method is developed and exploited for the synthesis of indole derivatives via microwave-assisted technology. By considering the advantage microwave synthesis in terms of high efficient energy, indole derivatives are prepared. In the current study, the Schiff's bases are first synthesized by reaction of 1H-indole-2,3-dione (isatin) with various substituted anilines in presence of acetic acid under microwave irradiation. Then the Mannich bases are produced by condensation of Schiff bases with different secondary amines in the presence of formaldehyde. The newly synthesized compounds are characterized by TLC report and spectral data followed by evaluation for anthelmintic activity against Pheretima posthuma. Albendazole is used as standard drug for comparative study. The titled compounds are screened for anthelmintic activity at the concentration of 10, 20 and 50 mg/ml. The anthelmintic effect of standard drug Albendazole is also evaluated at 10 mg/ml. The results of present study indicate that some of the tested compounds exhibit significant anthelmintic activity in dose dependent manner.

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