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5973-53-5

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5973-53-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 5973-53-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,9,7 and 3 respectively; the second part has 2 digits, 5 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 5973-53:
(6*5)+(5*9)+(4*7)+(3*3)+(2*5)+(1*3)=125
125 % 10 = 5
So 5973-53-5 is a valid CAS Registry Number.

5973-53-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 2,6-dinitro-N-pentan-3-yl-4-(trifluoromethyl)aniline

1.2 Other means of identification

Product number -
Other names Benzenamine,N-(1-ethylpropyl)-2,6-dinitro-4-(trifluoromethyl)

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:5973-53-5 SDS

5973-53-5Downstream Products

5973-53-5Relevant articles and documents

Synthesis and evaluation of dinitroanilines for treatment of cryptosporidiosis

Benbow, John W.,Bernberg, Erin L.,Korda, Anna,Mead, Jan R.

, p. 339 - 343 (2007/10/03)

The efficacy of a series of dinitroaniline herbicide derivatives for the treatment of Cryptosporidium parvum infections has been studied. The lead compounds oryzalin (compound 1) and trifluralin (compound 2) have low water solubility (3 ppm) which was alleged to be a major contributor to their poor pharmacokinetic availability. Derivatives of compounds 1 and 2 were synthesized. In these derivatives the functionality at the C-1 amine position or the C-4 position was substituted with groups with various hydrophilicities to determine if a direct relation existed between water solubility and overall activity. The chlorinated precursors of these derivatives were also examined and were found to be less active in the C. parvum assays, a result in direct contrast to earlier work with Leishmania. Enhanced water solubility alone did not overcome the drug availability problem; however, several candidates with similar activities but with toxicities lower than those of the lead compounds were produced.

4-Trifluoromethyl-2,6-dinitroanilines

-

, (2008/06/13)

This invention relates to a group of novel substituent anilines, useful in eliminating germinating and seedling weed grasses and selected broadleaf weeds.

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