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1503-84-0

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1503-84-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1503-84-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,5,0 and 3 respectively; the second part has 2 digits, 8 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 1503-84:
(6*1)+(5*5)+(4*0)+(3*3)+(2*8)+(1*4)=60
60 % 10 = 0
So 1503-84-0 is a valid CAS Registry Number.

1503-84-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name phenyl anthracene-9-carboxylate

1.2 Other means of identification

Product number -
Other names 9-Anthracenecarboxylic acid,phenyl ester

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:1503-84-0 SDS

1503-84-0Downstream Products

1503-84-0Relevant articles and documents

The novel anthracene decorated dendrimeric cyclophosphazenes for highly selective sensing of 2,4,6-trinitrotoluene (TNT)

?zcan, Emrah,Tümay, Süreyya O?uz,Ke?an, Gürkan,Ye?ilot, Serkan,?o?ut, Bünyemin

, (2019)

Novel fluorescent anthracene-decorated cyclotri- and cyclotetraphosphazenes (5 and 6) are designed and synthesized, and their chemosensor behaviors against nitroaromatic compounds are examined by UV/Vis and fluorescence spectroscopies for addressing the s

Metal-free synthesis of aryl esters from carboxylic acids and diaryliodonium salts

Petersen, Tue B.,Khan, Rehan,Olofsson, Berit

, p. 3462 - 3465 (2011/08/07)

An efficient arylation of carboxylic acids with diaryliodonium salts has been developed, giving aryl esters in high yields within short reaction times for both aromatic and aliphatic substrates. The transition-metal-free conditions are compatible with a range of functional groups, and good chemoselectivity is observed with unsymmetric diaryliodonium salts. Furthermore, steric hindrance in the ortho positions is well tolerated both in the carboxylic acid and in the diaryliodonium salt, yielding aryl esters that cannot be obtained via other esterification protocols.

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