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1-Naphthalenesulfonamide, 5-amino-N-(2,3-dimethylphenyl)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

648899-07-4

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648899-07-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 648899-07-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 6,4,8,8,9 and 9 respectively; the second part has 2 digits, 0 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 648899-07:
(8*6)+(7*4)+(6*8)+(5*8)+(4*9)+(3*9)+(2*0)+(1*7)=234
234 % 10 = 4
So 648899-07-4 is a valid CAS Registry Number.

648899-07-4SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 5-amino-N-(2,3-dimethylphenyl)naphthalene-1-sulfonamide

1.2 Other means of identification

Product number -
Other names 1-Naphthalenesulfonamide,5-amino-N-(2,3-dimethylphenyl)

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:648899-07-4 SDS

648899-07-4Downstream Products

648899-07-4Relevant academic research and scientific papers

Caffeoyl naphthalenesulfonamide derivatives as HIV integrase inhibitors

Xu, Yu-Wen,Zhao, Gui-Sen,Shin, Cha-Gyun,Zang, Heng-Chang,Lee, Chong-Kyo,Lee, Yong Sup

, p. 3589 - 3593 (2007/10/03)

HIV-1 integrase (IN) is an essential enzyme for retroviral replication and a rational target for the design of anti-AIDS drugs. In the present study, we have designed, synthesized and tested a series of caffeoyl naphthalenesulfonamide derivatives as HIV integrase inhibitors. Among these compounds, we found that HIV integrase inhibitory activities of compounds III-3 and III-4 were more potent than L-chicoric acid (IC50=11.8 μg/mL) and others were comparable to L-chicoric acid. Furthermore, the structure-activity relationships of these compounds were studied. The information gathered from this paper will be useful in the development and design of HIV-1 integrase inhibitors in the future.

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