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Azulene, 1-chloro- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

23306-02-7

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23306-02-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 23306-02-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,3,3,0 and 6 respectively; the second part has 2 digits, 0 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 23306-02:
(7*2)+(6*3)+(5*3)+(4*0)+(3*6)+(2*0)+(1*2)=67
67 % 10 = 7
So 23306-02-7 is a valid CAS Registry Number.

23306-02-7SDS

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 1-chloroazulene

1.2 Other means of identification

Product number -
Other names 1-Chlor-azulen

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:23306-02-7 SDS

23306-02-7Upstream product

23306-02-7Relevant academic research and scientific papers

Solution Photochemistry of Azulene

Selco, J. I.,Brooks, T.,Chang, M.,Trieu, M. T.,McDonald, J. K.,McManus, S. P.

, p. 429 - 433 (1994)

Photochemical reactivity has been observed in solution-phase azulene.Experiments are described which confirm photoinduced deuteration, chlorination, and polymerization.The threshold for the observed chemistry is at the origin of S2 which is at 27956 +/- 8 cm-1 (357.7 +/- 0.1 nm) in chloroform.Only one photon is required to induce the observed chlorine substitution reactions.Although no naphthalene is formed, this chemical channel appears to be the equivalent of a thermal reaction, with the substitutions taking place at the two equivalent positions on the small ring of azulene.The mechanism of these reactions is bimolecular in nature.Chlorination provides a complex mixture of products in most cases; however, deuteration proceeds cleanly giving only 1,3-d2-azulene.

Azulene – Thiophene – Cyanoacrylic acid dyes with donor-π-acceptor structures. Synthesis, characterisation and evaluation in dye-sensitized solar cells

Cowper, Paul,Pockett, Adam,Kociok-K?hn, Gabriele,Cameron, Petra J.,Lewis, Simon E.

supporting information, p. 2775 - 2786 (2018/05/04)

We report the synthesis of five new azulene containing dyes, having D-π-A type structures. These dyes are synthesised using a sulfonium salt cross-coupling reaction. The dyes have been evaluated spectroscopically, electrochemically, crystallographically, and as sensitizers in dye-sensitized solar cells. We propose a rationale for the dyes’ spectroscopic properties and performance in cells, based on conformational data derived from their crystal structures.

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