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3624-26-8

1,2-Ethanediol, 1,2-di-2-naphthalenyl- is a complex organic compound characterized by its unique structure. It features a central ethylene glycol (1,2-ethanediol) backbone, with each hydroxyl group (-OH) attached to a naphthalene ring. The naphthalene rings are substituted at the 2-position, meaning they are attached to the second carbon of the ethylene glycol. 1,2-Ethanediol,1,2-di-2-naphthalenyl- is known for its rigid structure due to the fused aromatic rings and is used in various applications, including as a chemical intermediate in the synthesis of dyes and pharmaceuticals. Its chemical formula is C18H14O2, reflecting the presence of 18 carbon atoms, 14 hydrogen atoms, and 2 oxygen atoms. The compound's properties, such as solubility and reactivity, are influenced by the presence of the naphthalene rings, which contribute to its stability and potential applications in the chemical industry.

3624-26-8

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3624-26-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 3624-26-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,6,2 and 4 respectively; the second part has 2 digits, 2 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 3624-26:
(6*3)+(5*6)+(4*2)+(3*4)+(2*2)+(1*6)=78
78 % 10 = 8
So 3624-26-8 is a valid CAS Registry Number.

3624-26-8SDS

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 β,β'-dihydronaphthoin

1.2 Other means of identification

Product number -
Other names 1,2-Dihydroxy-1,2-di-(naphthyl-(2))-aethan

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

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:3624-26-8 SDS

3624-26-8Relevant articles and documents

Application of coumarin dyes for organic photoredox catalysis

Gualandi, Andrea,Rodeghiero, Giacomo,Della Rocca, Emanuele,Bertoni, Francesco,Marchini, Marianna,Perciaccante, Rossana,Jansen, Thomas Paul,Ceroni, Paola,Cozzi, Pier Giorgio

, p. 10044 - 10047 (2018)

Here we report the application of readily prepared and available coumarin dyes for photoredox catalysis, which are able to mimic powerful reductant [Ir(iii)] complexes. Coumarin derivatives 9 and 10 were employed as photoreductants in pinacol coupling and in other reactions, in the presence of Et3N as a sacrificial reducing agent. As the electronic, photophysical, and steric properties of coumarins could be varied, a wide applicability to several classes of photoredox reactions is predicted.

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