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Methyl (5E)-5-{[2-(benzyloxy)phenyl]methylidene}-2-methyl-4-oxo-4,5-dihydro-1H-pyrrole-3-carboxylate is a complex organic compound with the molecular formula C21H19NO4. It features a pyrrole ring, which is a five-membered aromatic ring containing one nitrogen atom, and a carboxylate group attached to the methyl group. The compound also has a 5E configuration, indicating the presence of a trans double bond between the pyrrole ring and the phenyl group. The phenyl group is further modified with a benzyloxy substituent, which is a benzyl group attached to an oxygen atom. This chemical is primarily used in the synthesis of various pharmaceuticals and biologically active compounds due to its unique structure and reactivity.

6537-59-3

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6537-59-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 6537-59-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,5,3 and 7 respectively; the second part has 2 digits, 5 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 6537-59:
(6*6)+(5*5)+(4*3)+(3*7)+(2*5)+(1*9)=113
113 % 10 = 3
So 6537-59-3 is a valid CAS Registry Number.

6537-59-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name Benzo[g]quinazoline-5,10-dione

1.2 Other means of identification

Product number -
Other names -

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

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More Details:6537-59-3 SDS

6537-59-3Downstream Products

6537-59-3Relevant academic research and scientific papers

Cycloaddition Routes to Azaanthraquinone Derivatives. 1. Use of Azadienophiles

Potts, Kevin T.,Bhattacharjee, Debkumar,Walsh, Eileen B.

, p. 2011 - 2021 (2007/10/02)

The mono- and diazanaphthoquinones underwent facile cycloaddition with cyclic and alicyclic dienes, and in the majority of these cycloadditions the initial 1:1-cycloadducts or their tautomers and intermediate products formed in the oxidation procedure leading to the final azaanthraquinones were isolated.Quinoline-5,8-dione and 1-methoxy-1,3-cyclohexadiene gave the 8-methoxy isomer in an essentially regiospecific cycloaddition; isoquinoline-5,8-dione, however, gave both the 5- and 8-methoxy isomers in a 2.8:1 ratio.These structural assignments were verified by alternative syntheses of the possible isomers using heteroatom-directed lithiation procedures.

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