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Ethyl 2-(3-chloro-1,4-dioxo-1,4-dihydronaphthalen-2-yl)-3-oxobutanoate is a complex organic compound with the molecular formula C14H11ClO5. It is a derivative of naphthalene, a polycyclic aromatic hydrocarbon, with a chloro substituent at the 3-position and a 1,4-dihydronaphthalene structure. The compound features a 3-oxobutanoate group attached to the 2-position of the naphthalene ring, which is further esterified with an ethyl group. This chemical is characterized by its unique structure and functional groups, which may have potential applications in various chemical and pharmaceutical industries. However, further research and analysis are required to determine its specific uses and properties.

4660-46-2

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4660-46-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 4660-46-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,6,6 and 0 respectively; the second part has 2 digits, 4 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 4660-46:
(6*4)+(5*6)+(4*6)+(3*0)+(2*4)+(1*6)=92
92 % 10 = 2
So 4660-46-2 is a valid CAS Registry Number.

4660-46-2SDS

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 ethyl 2-(3-chloro-1,4-dioxonaphthalen-2-yl)-3-oxobutanoate

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:4660-46-2 SDS

4660-46-2Downstream Products

4660-46-2Relevant academic research and scientific papers

Vicarious nucleophilic substitution of hydrogen (VNS) in 1,4-naphthoquinone derivatives - Competition between VNS and vinylic nucleophilic substitution (SNV)

Ma?kosza, Mieczys?aw,Nizamov, Shamil

, p. 9615 - 9621 (2001)

Carbanions of dimethyl chloromalonate, ethyl 2-chloroacetoacetate and dimethyl malonate react with naphthoquinone derivatives mainly via vicarious nucleophilic substitution or oxidative nucleophilic substitution of hydrogen processes. These reactions in 2

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