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2,5-Pyrrolidinedione, 1-[(2,4-dimethoxyphenyl)methyl]- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

684287-65-8

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684287-65-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 684287-65-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 6,8,4,2,8 and 7 respectively; the second part has 2 digits, 6 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 684287-65:
(8*6)+(7*8)+(6*4)+(5*2)+(4*8)+(3*7)+(2*6)+(1*5)=208
208 % 10 = 8
So 684287-65-8 is a valid CAS Registry Number.

684287-65-8SDS

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 1-(2,4-dimethoxybenzyl)pyrrolidine-2,5-dione

1.2 Other means of identification

Product number -
Other names 1-(2,4-Dimethoxy-benzyl)-pyrrolidine-2,5-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:684287-65-8 SDS

684287-65-8Downstream Products

684287-65-8Relevant academic research and scientific papers

INHIBITORS OF IRES-MEDIATED PROTEIN SYNTHESIS

-

Page/Page column 38-40, (2017/12/18)

This disclosure relates to inhibitors of IRES-mediated protein synthesis, compositions comprising therapeutically effective amounts of these compounds, and methods of using those compounds and compositions in treating hyperproliferative disorders, e.g., cancers. This disclosure also relates to compositions comprising inhibitors of IRES-mediated protein synthesis and mTOR inhibitors, and to methods of treating cancer by conjoint administration of inhibitors of IRES-mediated protein synthesis and mTOR inhibitors.

Tricyclic HIV integrase inhibitors V. SAR studies on the benzyl moiety

Jin, Haolun,Metobo, Sammy,Jabri, Salman,Mish, Michael,Lansdown, Rachael,Chen, Xiaowu,Tsiang, Manuel,Wright, Matthew,Kim, Choung U.

body text, p. 2263 - 2265 (2009/12/07)

SAR studies on the para-fluorobenzyl moiety of tricyclic HIV integrase inhibitors are discussed and lead compounds with potency and PK properties comparable to raltegravir were identified.

Integrase inhibitor compounds

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Page/Page column 78, (2010/11/26)

Tricyclic compounds, protected intermediates thereof, and methods for inhibition of HIV-integrase are disclosed.

PHOSPHONATE ANALOGS OF HIV INTEGRASE INHIBITOR COMPOUNDS

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Page/Page column 571, (2010/02/15)

Novel HIV integrase inhibitor compounds having at least one phosphonate group, protected intermediates thereof, and methods for inhibition of HIV-integrase are disclosed.

Design and optimization of tricyclic phtalimide analogues as novel inhibitors of HIV-1 integrase

Verschueren, Wim G.,Dierynck, Inge,Amssoms, Katie I. E.,Hu, Lili,Boonants, Paul M. J. G.,Pille, Geert M. E.,Daeyaert, Frits F. D.,Hertogs, Kurt,Surleraux, Dominique L. N. G.,Wigerinck, Piet B. T. P.

, p. 1930 - 1940 (2007/10/03)

Human immunodeficiency virus type-1 integrase is an essential enzyme for effective viral replication and hence a valid target for the design of inhibitors. We report here on the design and synthesis of a novel series of phthalimide analogues as integrase

PRE-ORGANIZED TRICYCLIC INTEGRASE INHIBITOR COMPOUNDS

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Page 332;333, (2008/06/13)

Tricyclic compounds according to the structure below, protected intermediates thereof, and methods for inhibition of HIV-integrase are disclosed. Formula (I). Al and A2 are moieties forming a five, six, or seven membered ring. L is a bond or a linker connecting a ring atom of Ar to N. X is O, S, or substituted nitrogen. Ar is aryl or heteroaryl. Q is N, +NR, or CR4. The aryl carbons may be independently substituted with substituents other than hydrogen. The compounds may include prodrug moieties covalently attached at any site.

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