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10499-33-9

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10499-33-9 Usage

Description

(NE)-N-(2-chlorocyclooctylidene)hydroxylamine, with the molecular formula C8H15ClNO, is an organic hydroxylamine compound characterized by the presence of a cyclooct-3-en-1-ylidene group and a chlorine atom attached to the cyclooctene ring. (NE)-N-(2-chlorocyclooctylidene)hydroxylamine has garnered interest due to its potential as a radical scavenger, antioxidant, anti-inflammatory, and anti-cancer agent. Its unique molecular structure and properties render it a promising candidate for pharmaceutical research and applications.

Uses

Used in Pharmaceutical Industry:
(NE)-N-(2-chlorocyclooctylidene)hydroxylamine is used as a potential therapeutic agent for its antioxidant properties. Its ability to act as a radical scavenger makes it a candidate for the treatment of conditions associated with oxidative stress and free radical damage.
(NE)-N-(2-chlorocyclooctylidene)hydroxylamine is also used as an anti-inflammatory agent, leveraging its potential to reduce inflammation and alleviate symptoms in various inflammatory diseases.
Furthermore, (NE)-N-(2-chlorocyclooctylidene)hydroxylamine is used as an anti-cancer agent, with studies exploring its potential to target and inhibit cancer cell growth, making it a candidate for cancer treatment and prevention.
Used in Chemical Research:
In the field of chemical research, (NE)-N-(2-chlorocyclooctylidene)hydroxylamine serves as a subject of study for understanding its antioxidant, anti-inflammatory, and anti-cancer mechanisms. This knowledge can contribute to the development of novel pharmaceutical compounds and therapies.
Used in Material Science:
The unique properties of (NE)-N-(2-chlorocyclooctylidene)hydroxylamine may also find applications in material science, particularly in the development of new materials with antioxidant and anti-inflammatory characteristics for various industrial and consumer products.

Check Digit Verification of cas no

The CAS Registry Mumber 10499-33-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,0,4,9 and 9 respectively; the second part has 2 digits, 3 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 10499-33:
(7*1)+(6*0)+(5*4)+(4*9)+(3*9)+(2*3)+(1*3)=99
99 % 10 = 9
So 10499-33-9 is a valid CAS Registry Number.
InChI:InChI=1/C8H14ClNO/c9-7-5-3-1-2-4-6-8(7)10-11/h7,11H,1-6H2/b10-8-

10499-33-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name α-Chlorocyclooctanone oxime

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

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

More Details:10499-33-9 SDS

10499-33-9Relevant articles and documents

Oxidation of gem-chloronitroso- and vic-chloronitroso-alkanes and -cycloalkanes to respective chloronitro compounds by novel cetyltrimethylammonium hypochlorite reagent

Mohammed, Abdulkarim H.A.,Nagendrappa, Gopalpur

experimental part, p. 433 - 441 (2012/03/26)

Cetyltrimethylammonium hypochlorite (CTAHC) is prepared and used as an oxidizing agent for nitroso group to nitro group. The gem-chloronitroso and vic-chloronitroso compounds are prepared respectively from ketoximes and olefins by reacting with NOCl generated in situ from chlorotrimethylsilane (TMSC1 (l) and iso-amyl nitrite. CTAHC oxidizes gem-chloronitroso and vic-chloronitroso compounds to the corresponding chloronitro derivatives. While gem-chloronitro compounds are obtained in good yields, the vic-chloronitro derivatives are formed in moderate yields, because of the propensity of the vic-chloronitroso group to tautomerize to α-chlorooxime. The present method is simple and practical, particularly for the preparation of vic-chloronitro compounds, considering the fact that the known methods of their preparation are few and quite involved. Indian Academy of Sciences.

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