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1-(phenylsulfinyl)azulene is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

10437-67-9

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10437-67-9 Usage

Family

Azulene family

Structure

Seven-membered ring containing five carbon atoms and two nitrogen atoms, with a sulfur atom bonded to a phenyl group

Color

Pale yellow

Physical state

Solid

Solubility

Insoluble in water, soluble in organic solvents

Potential applications

Pharmaceutical and biological activities

Anti-inflammatory properties

Shown promising results as an anti-inflammatory agent

Antiviral properties

Shown promising results as an antiviral agent

Research areas

Organic synthesis and material science

Check Digit Verification of cas no

The CAS Registry Mumber 10437-67-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,0,4,3 and 7 respectively; the second part has 2 digits, 6 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 10437-67:
(7*1)+(6*0)+(5*4)+(4*3)+(3*7)+(2*6)+(1*7)=79
79 % 10 = 9
So 10437-67-9 is a valid CAS Registry Number.

10437-67-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-(benzenesulfinyl)azulene

1.2 Other means of identification

Product number -
Other names 1-azulenyl phenyl sulfoxide

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:10437-67-9 SDS

10437-67-9Upstream product

10437-67-9Relevant academic research and scientific papers

Synthesis and redox behavior of 1-azulenyl sulfides and efficient synthesis of 1,1′-biazulenes

Shoji, Taku,Higashi, Junya,Ito, Shunji,Toyota, Kozo,Asao, Toyonobu,Yasunami, Masafumi,Fujimori, Kunihide,Morita, Noboru

experimental part, p. 1242 - 1252 (2009/04/07)

The reaction of azulenes with several sulfoxides in the presence of acid anhydrides to afford the corresponding 1-azulenylsulfonium and 1,3-azulenediyldisulfonium ions is reported. The subsequent conversion of these ions in high yields into 1-azulenyl met

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