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36340-59-7

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36340-59-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 36340-59-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,6,3,4 and 0 respectively; the second part has 2 digits, 5 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 36340-59:
(7*3)+(6*6)+(5*3)+(4*4)+(3*0)+(2*5)+(1*9)=107
107 % 10 = 7
So 36340-59-7 is a valid CAS Registry Number.

36340-59-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-(1,3-dioxoisoindolin-2-yl)-N-(2-thiazolyl)benzenesulfonamide

1.2 Other means of identification

Product number -
Other names N,N-Phthaloyl-sulfanilsaeure-thiazol-2-ylamid

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:36340-59-7 SDS

36340-59-7Downstream Products

36340-59-7Relevant articles and documents

Synthesis and antimycobacterial activity of some phthalimide derivatives

Akgün, Hülya,Karamelekoglu, Irem,Berk, Barkin,Kurnaz, I?il,Saribiyik, Gizem,?ktem, Sinem,Kocag?z, Tanil

experimental part, p. 4149 - 4154 (2012/09/08)

Structurally modified phthalimide derivatives were prepared through condensation of phthalic and tetrafluorophthalic anhydride with selected sulfonamides with variable yields. All compounds were screened for their antimycobacterium activity against Mycobacterium tuberculosis H37Ra (ATCC 25177) using a micro broth dilution technique. The fluorinated derivatives (compounds 2c, 2d, 2f and 2h) had antimycobacterium activity comparable with classical sulfonamide drugs. The minimum inhibitory concentration (MIC) of compounds 2c, 2d, 2f and 2h was greater than that of isoniazid (MIC 0.02 μg/mL) and in vitro activity was greater than that of pyrazinamide, another first line antimycobacterium drug (MIC 50-100 μg/mL). The new compounds could be considered new lead compounds in the treatment of multi-drug resistant tuberculosis.

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