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Benzenamine, 4-(9H-pyrido[3,4-b]indol-1-yl)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

771533-61-0

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771533-61-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 771533-61-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 7,7,1,5,3 and 3 respectively; the second part has 2 digits, 6 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 771533-61:
(8*7)+(7*7)+(6*1)+(5*5)+(4*3)+(3*3)+(2*6)+(1*1)=170
170 % 10 = 0
So 771533-61-0 is a valid CAS Registry Number.

771533-61-0SDS

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 4-(9H-pyrido[3,4-b]indol-1-yl)aniline

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:771533-61-0 SDS

771533-61-0Relevant academic research and scientific papers

Synthesis and anti-leishmanial activity of 1-aryl-β-carboline derivatives against Leishmania donovani

Gohil, Vikrantsinh M.,Brahmbhatt, Keyur G.,Loiseau, Philippe M.,Bhutani, Kamlesh K.

, p. 3905 - 3907 (2012/07/03)

β-carbolines from various natural and synthetic sources have been known to show diverse biological activities. As a part of our current ongoing project to search for potent natural product-derived anti-leishmanial compounds, we have synthesized a series of substituted 1-aryl-β-carboline derivatives. A total of 22 compounds were synthesized and tested in vitro against Leishmania donovani, out of which 6 compounds (4, 5, 10, 11, 19 and 22) showed notably more activity than the standard miltefosine (IC50 12.07 ± 0.82 μM), with compound 4 being the most potent (IC 50 2.16 ± 0.26 μM).

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