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2-(phenylsulfinyl)-1-oxaspiro[2.5]octane is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

21849-30-9

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21849-30-9 Usage

Type of Drug

Nonsteroidal anti-inflammatory drug (NSAID)

Purpose

To reduce pain, inflammation, and stiffness caused by conditions such as arthritis, gout, and ankylosing spondylitis

Mechanism of Action

Inhibits the production of prostaglandins, which promote inflammation, pain, and fever in the body

Potential Use

Cancer treatment, as it has shown promise in inhibiting the growth of tumor cells

Side Effects

Can cause stomach ulcers, gastrointestinal bleeding, and liver damage

Caution

Should be used with caution and under the guidance of a healthcare professional

Check Digit Verification of cas no

The CAS Registry Mumber 21849-30-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,1,8,4 and 9 respectively; the second part has 2 digits, 3 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 21849-30:
(7*2)+(6*1)+(5*8)+(4*4)+(3*9)+(2*3)+(1*0)=109
109 % 10 = 9
So 21849-30-9 is a valid CAS Registry Number.

21849-30-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-(benzenesulfinyl)-1-oxaspiro[2.5]octane

1.2 Other means of identification

Product number -
Other names 1-(benzenesulfinyl)-2-oxaspiro[2.5]octane

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:21849-30-9 SDS

21849-30-9Relevant academic research and scientific papers

α,β-Epoxy Sulfoxides as Useful Intermediates in Organic Synthesis. I. A Novel Synthesis of Dialkyl Ketones and a Synthesis of Aldehydes from Ketones by One Carbon Elongation

Satoh, Tsuyoshi,Kaneko, Youhei,Izawa, Takao,Sakata, Kiichi,Yamakawa, Koji

, p. 1983 - 1990 (2007/10/02)

Treatment of α,β-epoxy sulfoxides, prepared from 1-chloroalkyl phenyl sulfoxides with ketones or aldehydes, with sodium benzeneselenolate gives dialkyl ketones or aldehydes in good yields under mild conditions.The mechanism of this reaction and an application of this process to a formal total synthesis of dihydrojasmone are described.

IODOMETHYL PHENYL SULFOXIDE: REACTIVITY AND SYNTHETIC APPLICATIONS

Reutrakul, Vichai,Panyachotipun, Chitchanun,Hahnvajanawong, Viwat,Sotheeswaran, S.

, p. 1825 - 1828 (2007/10/02)

Lithio iodomethyl phenyl sulfoxides reacted with alkyl halides and carbonyl compounds to give adducts in good to moderate yields.Solvolysis of the carbonyl adducts led to sulfones or the ring expanded product.

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