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7-oxocyclohepta-1,3,5-trien-1-yl 4-methoxybenzoate is a complex organic chemical compound with the molecular formula C15H12O4. It is a derivative of 7-oxocyclohepta-1,3,5-trien-1-yl, which is a seven-membered ring with a carbonyl group at the 7-position, and 4-methoxybenzoate, which is a benzoic acid derivative with a methoxy group at the 4-position. 7-oxocyclohepta-1,3,5-trien-1-yl 4-methoxybenzoate is characterized by its aromatic structure and the presence of a carbonyl group, which contributes to its reactivity and potential applications in various chemical processes. It is important to note that the compound's properties, such as solubility, stability, and reactivity, can be influenced by the specific arrangement of its atoms and the presence of functional groups.

2961-86-6

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2961-86-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 2961-86-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,9,6 and 1 respectively; the second part has 2 digits, 8 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 2961-86:
(6*2)+(5*9)+(4*6)+(3*1)+(2*8)+(1*6)=106
106 % 10 = 6
So 2961-86-6 is a valid CAS Registry Number.

2961-86-6SDS

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 2-<4-Methoxy-benzoyloxy>-tropon

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:2961-86-6 SDS

2961-86-6Downstream Products

2961-86-6Relevant academic research and scientific papers

Synthesis and biological evaluation of O-alkylated tropolones and related α-ketohydroxy derivatives as ribonucleotide reductase inhibitors

Tamburlin-Thumin, Isabelle,Crozet, Michel P.,Barriere, Jean-Claude,Barreau, Michel,Riou, Jean-Francois,Lavelle, Francois

, p. 561 - 568 (2007/10/03)

A series of O-alkylated tropolones and related α-ketohydroxy compounds were evaluated for their biological activities and were shown to present an expected ribonucleotide reductase inhibition and cytotoxicity against some cancer cell lines but no antitubulin activity. Pharmacomodulation studies were realised to understand and enhance the observed activities. These original benzylic, heterocyclic and allylic compounds have been synthesised by a phase-transfer catalysed O-alkylation developed in our laboratories.

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