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6-bromophenanthrene-9-carboxylic acid is a chemical compound with the molecular formula C18H9BrO2. It is a derivative of phenanthrene with a carboxylic acid group and a bromine atom attached to its molecular structure.
Used in Organic Synthesis:
6-bromophenanthrene-9-carboxylic acid is used as a building block in organic synthesis for creating other organic compounds.
Used in Chemical Research:
6-bromophenanthrene-9-carboxylic acid is used as a research compound in chemical research to study its unique chemical properties and potential applications.
Used in Pharmaceutical Industry:
6-bromophenanthrene-9-carboxylic acid is used as a potential building block in the development of new drugs due to its unique chemical properties.
Used in Materials Science:
6-bromophenanthrene-9-carboxylic acid is used as a potential component in the development of new materials with specific properties.
Used in Agrochemicals:
6-bromophenanthrene-9-carboxylic acid is used as a potential building block in the development of new agrochemicals.

53581-38-7

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53581-38-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 53581-38-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,3,5,8 and 1 respectively; the second part has 2 digits, 3 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 53581-38:
(7*5)+(6*3)+(5*5)+(4*8)+(3*1)+(2*3)+(1*8)=127
127 % 10 = 7
So 53581-38-7 is a valid CAS Registry Number.

53581-38-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 6-bromophenanthrene-9-carboxylic acid

1.2 Other means of identification

Product number -
Other names 3-Brom-phenanthren-10-carbonsaeure

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:53581-38-7 SDS

53581-38-7Downstream Products

53581-38-7Relevant academic research and scientific papers

NOVEL MATERIALS FOR ORGANIC ELECTROLUMINESCENT DEVICES

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Page/Page column 0059; 0098-0102, (2017/01/05)

The present invention relates to the compounds of the formula (1) and to organic electroluminescent devices, in particular blue-emitting devices, in which these compounds are used as host material in the emitting layer and/or as electron-transport materia

Soluble Catalysts for Improved Pschorr Cyclizations

Wassmundt, Frederick W.,Kiesman, William F.

, p. 196 - 201 (2007/10/02)

Several improved catalysts for the Pschorr phenanthrene synthesis have been discovered; all are soluble substances which initiate free-radical reactions by electron donation and thereby shorten the reaction time and increase the yield.One technique with K

PHOTOCATALYSIS OF THE PSCHORR REACTION BY TRIS-(2,2'-BIPYRIDYL)RUTHENIUM(II) IN THE PHENANTHRENE SERIES

Cano-Yelo, Herminia,Deronzier, Alain

, p. 1093 - 1098 (2007/10/02)

The photocatalytic conversion of the tetrafluoroborate salt of the stilbenediazonium ion (1) into the corresponding phenanthrene (2) (Pschorr reaction) by Ru(bpy)3(2+) (bpy = 2,2'-bipyridyl) has been investigated.We have shown that this particular Pshorr

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