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162784-88-5

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162784-88-5 Usage

Potency

Potent fluorescence quencher

Applications

Used in biological and analytical applications

Photochemotherapeutic properties

Studied for potential use in cancer therapy

Antimicrobial and antifungal activities

Investigated for its potential in these areas

Versatility

Multifunctional chemical compound with potential applications in various fields

Check Digit Verification of cas no

The CAS Registry Mumber 162784-88-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,6,2,7,8 and 4 respectively; the second part has 2 digits, 8 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 162784-88:
(8*1)+(7*6)+(6*2)+(5*7)+(4*8)+(3*4)+(2*8)+(1*8)=165
165 % 10 = 5
So 162784-88-5 is a valid CAS Registry Number.

162784-88-5SDS

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 9-(2-nitrophenyl)-3,3,6,6-tetramethyl-3,4,6,7,9,10-hexahydro-1,8(2H,5H)acridinedione

1.2 Other means of identification

Product number -
Other names 3,3,6,6-tetramethyl-9-(2-nitrophenyl)-3,4,5,6,9,10-hexahydroacridine-1,8(2H,7H)-dione

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:162784-88-5 SDS

162784-88-5Downstream Products

162784-88-5Relevant articles and documents

Facile and simple route to the synthesis of condensed acridine systems

Murugan, Periyasamy,Hwang, Kuo Chu,Thirumalai, Dhakshanamurthy,Ramakrishnan, Vayalakavoor T.

, p. 1781 - 1788 (2005)

Condensation of cyclohexane-1,3-dione or dimedone with o-nitrobenzaldehyde and ammonium acetate/acetic anhydride furnished the corresponding acridinedione/xanthene derivatives. The middle ring aromatization followed by reductive cyclization afforded the r

An Efficient One-Pot Four-Component Synthesis of 9-Aryl-Hexahydroacridine-1,8-Dione Derivatives in the Presence of a Molecular Sieves Supported Iron Catalyst

Magyar, ágnes,Hell, Zoltán

, p. 2528 - 2534 (2019/06/19)

Abstract: A series of 9-aryl-hexahydroacridine-1,8-diones are synthetized with good to excellent yields (50–99%) via a one-pot four-component reaction of dimedone, aromatic aldehydes and ammonium acetate in the presence of 4?? molecular sieves modified wi

N-Propyl benzoguanamine sulfonic acid supported on magnetic Fe3O4 nanoparticles: A novel and efficient magnetically heterogeneous catalyst for the synthesis of 1,8-dioxo-decahydroacridine derivatives

Gholami Dehbalaei, Masoumeh,Foroughifar, Naser,Pasdar, Hoda,Khajeh-Amiri, Alireza

supporting information, p. 327 - 335 (2017/12/28)

In this study, N-propyl-benzoguanamine-SO3H-stabilized magnetic nanoparticles were prepared as a new heterogeneous acid catalyst in accordance with the principles of green chemistry. The new catalyst is used for the synthesis of derivatives of

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