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1,3-dichloro-6-(trifluoromethyl)phenanthren-9-carboxylic acid is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

38635-85-7

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38635-85-7 Usage

Molecular structure

Complex, polycyclic aromatic compound

Functional groups

Carboxylic acid, chlorine, and fluorine atoms

Usage

Primarily as a research reagent

Presence in commercial products

Not commonly found

Potential applications

Pharmaceuticals, organic synthesis, and material science

Notability

Unique structure and properties, but not widely used or well-known outside scientific research settings

Check Digit Verification of cas no

The CAS Registry Mumber 38635-85-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,8,6,3 and 5 respectively; the second part has 2 digits, 8 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 38635-85:
(7*3)+(6*8)+(5*6)+(4*3)+(3*5)+(2*8)+(1*5)=147
147 % 10 = 7
So 38635-85-7 is a valid CAS Registry Number.
InChI:InChI=1/C16H7Cl2F3O2/c17-8-4-11-10-3-7(16(19,20)21)1-2-9(10)13(15(22)23)6-12(11)14(18)5-8/h1-6H,(H,22,23)

38635-85-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 1,3-dichloro-6-(trifluoromethyl)phenanthrene-9-carboxylic acid

1.2 Other means of identification

Product number -
Other names EINECS 254-048-4

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:38635-85-7 SDS

38635-85-7Relevant academic research and scientific papers

3-Hydroxy-N′-arylidenepropanehydrazonamides with Halo-Substituted Phenanthrene Scaffolds Cure P. berghei Infected Mice When Administered Perorally

Leven, Michael,Knaab, Tanja C.,Held, Jana,Duffy, Sandra,Meister, Stephan,Fischli, Christoph,Meitzner, Diane,Lehmann, Ursula,Lungerich, Beate,Kuna, Krystina,Stahlke, Petra,Delves, Michael J.,Buchholz, Mirko,Winzeler, Elizabeth A.,Avery, Vicky M.,Mordmüller, Benjamin,Wittlin, Sergio,Kurz, Thomas

, p. 6036 - 6044 (2017/08/02)

Structural optimization of 3-hydroxy-N′-arylidenepropanehydrazonamides provided new analogs with nanomolar to subnanomolar antiplasmodial activity against asexual blood stages of Plasmodium falciparum, excellent parasite selectivity, and nanomolar activity against the earliest forms of gametocyte development. Particularly, derivatives with a 1,3-dihalo-6-trifluoromethylphenanthrene moiety showed outstanding in vivo properties and demonstrated in part curative activity in the Plasmodium berghei mouse model when administered perorally.

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