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2-bromo-3-(phenylsulfanyl)naphthalene-1,4-dione is a complex organic chemical compound characterized by a naphthalene core, which is a fused ring system consisting of two benzene rings. This particular compound features a bromine atom attached to the 2nd carbon of the naphthalene, a sulfur atom bonded to a phenyl group (benzene ring) at the 3rd carbon, and a 1,4-dione functional group, indicating two carbonyl groups (C=O) at the 1st and 4th positions of the naphthalene. The presence of the bromine and phenylsulfanyl groups imparts unique chemical and physical properties to the molecule, making it potentially useful in various applications such as pharmaceuticals, agrochemicals, or materials science.

3114-98-5

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3114-98-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 3114-98-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,1,1 and 4 respectively; the second part has 2 digits, 9 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 3114-98:
(6*3)+(5*1)+(4*1)+(3*4)+(2*9)+(1*8)=65
65 % 10 = 5
So 3114-98-5 is a valid CAS Registry Number.

3114-98-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-bromo-3-phenylsulfanylnaphthalene-1,4-dione

1.2 Other means of identification

Product number -
Other names 2-bromo-3-phenylthio-1,4-naphthoquinone

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:3114-98-5 SDS

3114-98-5Relevant academic research and scientific papers

Green synthesis of thiophenyl-1,4-naphthoquinones

Kanodia, Saraswati,Thapliyal, Prakash Chander

, p. 833 - 836 (2012/10/29)

Reaction of 1,4-naphthoquinones adsorbed on neutral alumina to thiophenols in ambient conditions gave respective mono thiophenyl 1,4-naphthoquinones regioselectively in quantitative yield. The solvent free synthesis and quantitative conversion makes the process practical method.

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