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Decahydro-1,8-biphenylene-dione, also known as 1,8-naphthoquinone, is an organic compound with the chemical formula C10H12O2. It is a white crystalline solid that is soluble in organic solvents and has a melting point of 97-99°C. DECAHYDROBIPHENYLENE-1,8-DIONE is a derivative of naphthalene, with two carbonyl groups (C=O) attached to the 1 and 8 positions of the molecule. Decahydro-1,8-biphenylene-dione is used in various applications, including as a chemical intermediate in the synthesis of dyes, pharmaceuticals, and other organic compounds. It is also known for its potential use as a redox mediator in electrochemical processes. Due to its reactivity, it is important to handle DECAHYDROBIPHENYLENE-1,8-DIONE with care, following proper safety protocols.

5230-92-2

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5230-92-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 5230-92-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,2,3 and 0 respectively; the second part has 2 digits, 9 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 5230-92:
(6*5)+(5*2)+(4*3)+(3*0)+(2*9)+(1*2)=72
72 % 10 = 2
So 5230-92-2 is a valid CAS Registry Number.

5230-92-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name Decahydrobiphenylene-1,8-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:5230-92-2 SDS

5230-92-2Upstream product

5230-92-2Downstream Products

5230-92-2Relevant academic research and scientific papers

Regioselective Photocyclodimerization of Cyclohexenones Intercalated on Clay Layers

Usami, Hisanao,Takagi, Katsuhiko,Sawaki, Yasuhiko

, p. 1405 - 1408 (2007/10/02)

UV light irradiation of 2-cyclohexenones (1) in the presence of saponite clay resulted in a regioselective photodimerization affording anti-head-to-head dimer.The directed intercalation of 1 was suggested by the regioselective dimerization, X-ray diffraction, IR and photoluminescence analyses.

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