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85438-53-5

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85438-53-5 Usage

Chemical Class

Isoindole derivatives

Physical State

White solid substance

Common Uses

Building block in the synthesis of pharmaceuticals and organic compounds, dye intermediate, pigment in manufacturing, production of agrochemicals and specialty chemicals

Known For

Versatile chemical properties and unique chemical structure.

Check Digit Verification of cas no

The CAS Registry Mumber 85438-53-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,5,4,3 and 8 respectively; the second part has 2 digits, 5 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 85438-53:
(7*8)+(6*5)+(5*4)+(4*3)+(3*8)+(2*5)+(1*3)=155
155 % 10 = 5
So 85438-53-5 is a valid CAS Registry Number.

85438-53-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-[4-[4-(1,3-dioxoisoindol-2-yl)phenyl]sulfonylphenyl]isoindole-1,3-dione

1.2 Other means of identification

Product number -
Other names N,N'-4,4'-diphenylenesulfonebisphthalimide

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:85438-53-5 SDS

85438-53-5Downstream Products

85438-53-5Relevant articles and documents

Synthesis and in vitro anti Mycobacterium tuberculosis activity of a series of phthalimide derivatives

Santos, Jean L.,Yamasaki, Paulo R.,Chin, Chung Man,Takashi, Celio H.,Pavan, Fernando R.,Leite, Clarice Q.F.

, p. 3795 - 3799 (2009)

New phthalimide derivatives were easily prepared through condensation of phthalic anhydride and selected amines with variable yields (70-90%). All compounds (3a-l) were evaluated against Mycobacterium tuberculosis H37Rv using Alamar Blue susceptibility. The compounds 3c, 3i, and 3l have the minimum inhibitory concentrations (MICs) of 3.9, 7.8, and 5.0 μg/mL, respectively, and could be considered new lead compounds in the treatment of tuberculosis and multi-drug resistant tuberculosis. Crown Copyright

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